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Cerebral Palsy and Neurodisability

STRUCTURAL CHANGES IN BRAIN ON CRANIAL MAGNETIC RESONANCE IMAGING (MRI) IN SEVERELY MALNOURISHED CHILDREN
Harshit Bhargava
Acute cerebral venous thrombosis and diffuse white matter changes in classic homocystinuria
Christopher Barton
Acetazolamide induced aseptic meningitis in a female adolescent with idiopathic intracranial hypertension
Christopher Barton
Intramyocellular lipid excess in the mitochondrial disorder MELAS: MRS determination at 7T.
Sailaja Golla, Craig Malloy, Jimin Ren, Juan Pascual
Autism Spectrum Disordes - what are we waiting for? : 5 year follow-up study
taras no voloshyn
Fine motor functioning and speech in patients with Autism spectrum disorders during treatment by Intensive Neurophysiological Rehabilitation System
Volodymyr no Kozyavkin
Acetazolamide for severe early-onset epileptic encephalopathy due to mutations in the KCNA2 gene
khalid jama hundallah
Applying the SCPE Brain MRI Classification System in Cerebral Palsy: a valid process for analyzing data from a Cerebral Palsy Registry.
Antigoni Syrigou Papavasileiou, Maria Koutsaki, Marianna Petra, Sotiria Mastroyianni, Maria Pyrgelli, George Damianos, Irene Nikaina, Helen Skouteli, Argirios Dinopoulos
Prevention and Cure of the Intrathecal Baclofen Pump .
Yasser Awaad
Synergetic effect of intrathecal baclofen and deep brain stimulation in treating dystonia
Yasser Awaad
Functional Assessment Following Intrathecal Baclofen Therapy in Children with Spastic Cerebral Palsy
Yasser Awaad
Botulinum toxin- A in postoperative pediatric stiff hips
Yasser Awaad
EFFICACY OF DEEP BRAIN STIMULATION(DBS) IN REFRACTORY PEDIATRIC DYSTONIA
Dr Tarishi Nemani, Dr Vishal Kanubhai Patel, Dr.Puja Mehta, Dr.Paresh Doshi, Dr.Anaita Udwadia Hegde
Bilateral Actigraphy as a Real-World Measure of Motor Asymmetry in Hemiparetic Children with Perinatal Stroke
Asha Hollis, Ephrem Zewdie, Adam Kirton
Frequency and predictive factors of scoliosis in Malaysian children with Cerebral Palsy
POORANI ANANDAKRISHNAN, TEIK BENG KHOO
Improving epilepsy control among children with Cerebral Palsy in rural Bangladesh
Tasneem Karim, Manik Chandra Das, Mohammad Muhit, Nadia Badawi, Gulam Khandaker, Shekeeb S Mohammad
Cognitive profile in children with bilateral spastic cerebral palsy due to periventricular leukomalacia
Kaeko Ogura, Yukihiro Kitai, Satori Hirai, Hiroshi Arai
Upper Limb Habilitation in Children with Hemiplegic Cerebral Palsy Using A Novel Robotic Device – Assessment Using Jebsen-Taylor and Bruininks-Oseretsky Tests
Hian-Tat ONG, Hian-Tat ONG, Jia Xuan Tan, Michelle Lee, Jeremy LIN, Chee Leong Teo, Etienne Burdet, Sam Shuzhi Ge
Long-term neurodevelopmental outcomes following Extracorporeal Life Support and the role of neuroimaging in predicting outcomes
Sailaja Golla, Lakshmi Raman, Archana Dhar, Pilar Martin, Mary Ann Morris, Jefferson Tweed, stacey scott, Vinai Modem
An Update of Epidemiology of Cerebral Palsy in Northern region of Bangladesh – A comparative analysis
Mohammad Abdul Wahed
An Update of Epidemiology of Cerebral Palsy in Northern region of Bangladesh – A comparative analysis
Mohammad Abdul Wahed
CT Scanning findings in clinically diagnosed Cerebral Palsy
Mohammad Abdul Wahed
Wasting Syndrome – A predictor of early death in Cerebral Palsy
Mohammad Abdul Wahed
Mobius syndrome in four cases and literature review
yang xinying
International classification of function (ICF) Its application in cerebral palsy and Validation of the core sets in the Pakistani population
Shahnaz Hamid Ibrahim
Association of Risk factors for Early Childhood Disability in Rural Pakistan
Shahnaz Hamid Ibrahim
Outcomes and SLC2A1 Mutations in Febrile Young Infants with Hypoglycorrhachia
WENHAO YU
ROLE OF LINGUISTIC PROFILING INASSESSMENTS OF LEARNING AND LANGUAGE DISORDERS IN INDIAN CHILDREN-A CASE CONTROL STUDY
MsNitya Raman, MONA GAJRE, DrNandini Singh
A qualitative study on the clinical, radiological characteristics, and Prevalence of co-morbid conditions in children with hemiplegic cerebral palsy
Tandra Harish Varma, PRATIBHA SINGHI, Naveen Sankhyan, Prabhjhot Malhi
Sensorimotor robotic measures of tDCS and HD-tDCS enhanced motor learning in children
Lauran Cole
Sleep Disorders in Children with Cerebral Palsy
Tanmay Sanjay Jadhav, Dr. Shilpa Kulkarni, Dr. Amit Bhondve
CASE CONTROL STUDY ON ANTHROPOMETRIC ASSESSMENT OF CHILDREN WITH CEREBRAL PALSY
Aritra Guha, Dipankar Gupta, Sankar Kumar Das
Prevalence and profile of sleep disorders in children with static encephalopathy (Cerebral palsy) at a tertiary care pediatric centre
lakshmi narayana indana, Ramesh Konanki, Lokesh Lingappa, Nikith Milind Shah, Raju B.S.C.P B
Brain computer interface control in hemiparetic children with perinatal stroke
Zeanna Jadavji, Jack Zhang, Ephrem Zewdie, Adam Kirton
Preliminary Magnetoencephalography (MEG) Findings of Somatosensory Gating Using Dual-Pulse Sensory Tactile Stimulation in Dystonic Children with Basal Ganglia Stroke
Nomazulu Dlamini, Ahmad Mousa, Cecilia Jobst, Sabah Master, Gabrielle deVeber, Douglas Cheyne
Influence of plantar flexors spasticity on center of mass during walking among children with unilateral spastic cerebral palsy
Ehab Anwar Waly, Mai Ahmed
Genomic analysis identifies pathogenic variants in 9 of 17 cases with full-term cerebral palsy
Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata-Uematsu, Takehiko Inui, Saeko Yamamura-Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki-Muromoto, Yukimune Okubo, Wakaba Endo, Noriko Togashi, Yasuko Kobayashi, Akira Onuma, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Yoko Aoki, Shigeo Kure
Effect of structured weight bearing exercise on bone mineral density in children with Cerebral Palsy- an observational cohort
Ayush Gupta, U Singh, Biswaroop Chakrabarty, Prashant Jauhari, Atin Kumar, Manisha Jana, P Chaturvedi, Vandana Jain, R M Pandey, Sheffali Gulati
Which is the most common physiological type of Cerebral Palsy in India?
Mayank Vrujlal Detroja, Mahesh Kamate
General Movement Assessment in High Risk Infants in Sri Lanka: Experience from a Large Tertiary Care Hospital
gemunu prabhath hewawitharana, Piyumi Sasikala Wickramarachchi, Ayesha Yaddehi, R.D. Susantha Kumara, K.V. Kanchana Nilukshika, K.M.I. Induli, D.R. Sadeepi Chathuranga, D.L.N. Priyangika, W.R.A. Shantha, Sajee Anuradha Gamage, Bimba D.R. Hewawitharana, Champa J Wijesinghe
Association of comorbidities in cerebral palsy with GMFCS, CP type and Quality of life : An observational study at a tertiary care hospital
JAYANTI PRABHA, areesha alam, Rashmi Kumar, Chandrakanta kumar, neera kohli
Assessment of Neurodevelopmental Status in Infants and Children with Neonatal Hypoglycemic Brain Injury –characterise the Spectrum of Neurodisability (6-42 months)- Pilot Study
pradnya gadgil, Vidhi Shah, Shailee Shah, Abhishek Srivastava
Neurodevelopmental assessment of children and adolescents with Neonatal Hypoglycemic Brain Injury (NHBI) to establish the developmental profile in the age group of 6 years- 16 years: A Pilot Study
pradnya gadgil, Yuvika Kamdar, Pavitra Desai, Abhishek Srivastava
NEURO-DEVELOPMENTAL DELAY AND MALNUTRITION IN CHILDREN 0-6 YEARS IN MARGINALIZED RURAL INDIA
nandita chattopadhyay
Motor outcome after Therapeutic Hypothermia in infants with Hypoxic-Ischaemic Encephalopathy
Marieke Kuiper, Linda Meiners, Elizabeth Chandler, Rick Brandsma, Arend Bos, Hendrik ter Horst, Deborah Sival
Association of interleukin -6 Polymorphism and mRNA expression in cerebral palsy – a Pilot study
Anju Aggarwal, Sonali Verma, Anurupa Chakraborty, Neha Bansal, Shambhavi Roy
Efficacy of Botulinum Toxin on Spasticity and Functional Outcome in Cerebral Palsy: an evaluation
Lokesh Lingappa
A retrospective study to look for aetiology of cerebral palsy, time at diagnosis and the time taken to start rehabilitation services in patients following rehabilitation services at Lady Ridgeway Hospital, Colombo, Sri Lanka
Amali Dalpatadu, Samantha Waidyanatha, Pyara Ratnayaka, KCS Dalpatadu
Solution to problem of Plenty
Rahul Bharat
Home medical care for children with severe motor and mental disabilities
MARIKO MAEZAWA
Gabapentin in the management of dystonia: an open labeled study
payal shah, vrajesh udani, Alita Misquitta
Clinical course and seizure outcome of symptomatic epilepsy in cerebral palsy patients : community based study
Noha El tantawi, Dina Abd Elmegid
Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET), Central Motor Conduction Times (CMCT) and Somatosensory Evoked Potentials (SEP) in children with dystonic cerebral palsy (CP)
Stavros Tsagkaris, Verity McClelland, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Alexander Hammers, Jean-Pierre Lin
Neonatal Hypoglycemic Brain Injury in the indian scenario : Risk Factors And Clinical Profile
payal shah, vrajesh udani, Neelu Desai
ASSESSMENT OF IMPROVEMENT IN FUNCTIONAL ABILITY AND COMORBIDITIES OF A COHORT OF CHILDREN WITH CEREBRAL PALSY
PARVATHI MOHAN
From cerebral palsy to hereditary spastic paraplegia: à propos of three patients
Dina Rose Amrom, Sara Seneca, Cedric Ballez, Monique Cordonnier, Peter De Jonghe, Jonathan Baets, Massimo Pandolfo, Julie Soblet, Guillaume Smits
Clinical, radiological and genetic findings in a cohort of 60 polymicrogyria patients
Dina Rose Amrom, Annapurna Poduri, Nicolas Deconinck, Bernard Dan, Cynthia Prigogine, Anne Monier, Alec Aeby, Guillaume Smits, Emmanuel Scalais, Ingrid Unterberger, Eugen Trinka, François Dubeau, Donatella Tampieri, Jean-Claude Décarie, Jacques Michaud, Paul Mark, William B Dobyns, Christopher A Walsch, Frederick Andermann, Eva Andermann
Mothers’ perception in changes of hand skills pattern of their children with cerebral palsy to perform activities of daily living in Bangladesh
Md. Yeasir Arafat Alve
Integrative management of Cerebral palsy- Ayurveda (Indian traditional medicine) with Rehabilitative therapies
Lekshmi M K
Using Telemedicine to improve Access to Specialty Care for Underserved Patients with Neurodevelopmental Disorders.
Deepa Unnikrishnan Menon

CNS Infections

Neurodevelopment of 24 children born in Brazil with congenital Zika syndrome in 2015 - case series study
Lucas Victor Alves, Camila E Parede, Germanna V Silva, Maria Julia Gonçalves Mello, João Guilherme Bezerra Alves
Congenital Zika syndrome and infatile spasms - case series study
Lucas Victor Alves, Maria Júlia Gonçalves Mello, Patrícia Bezerra, João Guilherme Bezerra Alves
Perceptions and beliefs underpinning parents’ understanding about Neurocysticercosis among their children: A qualitative study
Endrakanti Mounika
Changing face of Pediatric Neurotuberculosis.
Kritika Tiwari, Purva Keni Karnavat, Anaita Udwadia Hegde
Chikungunya infection and Horner Syndrome: a case report
Lucas Victor Alves, Filipe Marinho Pinheiro Câmara, Mayara Batista Granhara, Alfredo Meneses Neto, João Guilherme Bezerra Alves
Reducing Turnaround Time (TAT) in the diagnosis of bacterial meningitis: Direct CSF analysis by Mass Spectrometry
Varnit Shanker
Should ionic calcium be a mandatory work up of suspected encephalitis
Varnit Shanker
G-Therapy: A Hope For Patients With Subacute Sclerosing Panencephalitis!
Gunvant Devichand Oswal, Dr.Pooja Shrirang Upasani, Dr. Umesh D. Kalane, Dr.Nandan Yardi, Dr. Anaita Udwadia Hegde
Serum and CSF concentrations of visinin-like protein-1 in children with acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) and those with prolonged febrile seizures
Takashi Ichiyama
Clinico-Radiological Profile and Outcome of Children with Tubercular Meningitis in a Tertiary Care Centre in Bangladesh
Kanij Fatema, Kanij Fatema, Md Mizanur Rahman
A case of mumps-related acute encephalopathy with biphasic seizures and late reduced diffusion
Takashi Shiihara
Good Hearing Outcome in Children with non-polio Enteroviral Meningitis
Chew Thye Choong, Elis Lee, Henry Tan, Natalie Tan
Should ionic calcium be a mandatory work up of suspected encephalitis
Varnit Shanker
Seasonal Influenza-Related Neurologic Complications in Children from 2010 to 2015
Eun Young Kim, Hui Jeong Yun, Hyung Min Cho
Polymerase Chain Reaction of cerebrospinal fluid in children with acute bacterial meningitis
Rajniti Prasad
A case of fulminant SSPE with transient EEG changes
Senthilkumar Vajramanickam
Differentiating Scrub typhus meningoencephalitis from other Acute Encephalitis Syndrome In children in Uttar Pradesh, India
Pranshi Agarwal, Areesha Alam, Jayanti Prabha, Amita Jain, Chandrakanta Kumar, Sanjeev Kumar Verma, Rashmi Kumar
Subacute Sclerosing Panencephalitis Presenting As Autoimmune Encephalitis
Ridhimaa Jain, Suvasini Sharma, Shilpa Devamare
Clinical profile and outcomes in Acute Necrotising Encephalopathy Of Childhood: Case series from a tertiary care Pediatric centre in India
srikanth domala
Rare case of streptococcus pneumoniae brain abscess in an infant
Surabhi Kaul, Rajan P Patel, Ian J Butler
A new mouse model of congenital Zika virus infection reveals neurodevelopmental pathways disrupted in congenital Zika syndrome
Ganeshwaran Hitoshi Mochida, Tojo Nakayama, Amanda Guise, Kimino Fujimura, Anais Meziani, Long Cheng, Dylan Vaughan, Andrew Kodani, Ann Durbin, Irene Bosch, Mauro Teixeira, Hanno Steen, Lee Gehrke, Judith Steen
A CASE SERIES OF EOSINOPHILIC MENINGITIS IN SOUTH INDIAN CHILDREN
sai chandar dudipala
SUBACUTE SCLEROSING PANENCEPHALITIS IN POST-MEASLES VACCINATION ERA-THE CHANGING EPIDEMIOLOGICAL TRENDS AND NEED FOR EARLY VACCINATION
EKTA AGARWAL, Dr. Kavita Srivastav, Dr. Surekha Rajadhyaksha
Atypical CNS infection: needs a mention.
abhijeet vilas botre
AUTOIMMUNE ENCEPHALITIS, AN EASILY OVERLOOKED ENTITY
Fadila Sufyan
Perceptions and beliefs underpinning parents’ understanding about Neurocysticercosis among their children: A qualitative study
Endrakanti Mounika
Congenital CMV infection- A rare cause of Central Diabetes Insipidus
Ambrin Akhtar
Japanese Encephalitis with Neurocysticercosis- Coexistence or Coincidence
MAROTI KADAM, Rajwanti K Vaswani, Shagun Shah, Baliram Gore, Chandrahas T Deshmukh, Jane David
Meningitis in patients with cerebral palsy: a review of eighteen cases from a single institution
Varnit Shanker
Treatment outcome of children with Congenital CMV infection at ICH and Dr. MR Khan Shishu(Children) Hospital
MASHAYA ZAMAN KOLI, SELINA HUSNA BANU, RAWNAK ARA
Cytokine and chemokine responses in clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) by type
Shinichiro Morichi
A case series of CNS influenza (H1N1) infection.
abhijeet vilas botre
ANALYSIS OF 126 CASES OF “ACTUTE ENCEPHALITIS SYNDROME” IN A PEDIATRIC ICU.
Ramakant Sabharwal, Praveen Kumar, SUMIT BHOJWANI, Sapna jain
Clinico-epidemiological profile and outcome of pediatric neurotuberculosis: a retrospective cohort study
Biswaroop Chakrabarty, Vivek Sirolia, Mudit Aggarwal, Prashant Jauhari, Atin Kumar, Sheffali Gulati
complete remission of a case of SSPE with intrathecal interferon alpha.
Nirendra Kumar Rai, ruchi singh
BILATERAL STRIATAL BRAIN ABSCESS- A RARE SITE, A RARE ORGANISM
Srinivasavaradan Govindarajan, INDRABHUSHAN SINGH, KANIKA GOYAL, ARUSHI GAHLOT SAINI, RENU SUTHAR, SAMEER VYAS, JAYASHREE MURALIDHARAN, MEENU SINGH
Clinical Outcome at 18 months following Acute Flaccid Myelitis due to Enterovirus D68
Jay Shetty, Lauren Marie Smith, Jacqueline McPherson, Paul Eunson, Kenneth McWilliam, Catherine McDougall, Kate Templeton
YIELD OF GENEXPERT AND OUTCOMES IN PEDIATRIC TUBERCULAR MENINGITIS
Lokesh Lingappa
High burden of neurological presentations in children admitted to Kenyan hospitals: A multi-hospital cohort study.
Jane Hassell, Thomas Julius, Morris Ogero, Charles RJC Newton, Mike English, Sam Akech
Enterovirus-D68 associated acute flaccid myelitis in Europe- Clinical and epidemiological data from European Collaboration
Jay Shetty, Marjolein Knoester, Jelte Helfferich, Oebele Brouwer, Coretta Van Leer-Buter, Randy Poelman, Hubert Niesters, EU EV D68 Working Group
A prospective cohort study to assess seizure recurrences in children with calcified neurocysticercosis
Abhijit Modak, Renu Suthar, Jitendra Kumar Sahu, Naveen Sankhyan, Niranjan Khandelwal
SSPE mimicking anti-NMDA receptor encephalitis
Shilpa Devamare, Vikram Bhaskar, Himani Bhasin, Suvasini Sharma
Syndromic Evaluations of CNS Infections by Multiplexed PCR Panels Enable Rapid Detection and Treatment of Infections
Siddhesh Chorghe, Sumir Pandit, Ashwini Chawathe, Pooja Gowda, Aparna Kotekar
Brachial neuritis and Prolonged Survival: The Enigma of Rabies encephalomyelitis
Kanika Goel, Chandana Bhagwat, Arushi Gahlot Saini, Renu Suthar, Reeta Mani, Paramjeet Singh, Namita Ravikumar, Meenu Singh
A prospective cohort study to assess seizure recurrences in children with calcified neurocysticercosis
Abhijit Modak, Renu Suthar, Jitendra Kumar Sahu, Naveen Sankhyan, Niranjan Khandelwal
Post infectious Opsoclonus Myoclonus Ataxia Syndrome in Tropics
Sumeet Dhawan, Lokesh Saini, Prabhudev M Hiremath, Bhanudeep singanamala, Arundhati Mukherjee, Sameer Vyas, Jitendra Sahu, Jayashree M, Naveen Sankhyan
What is the optimal duration of Anti-convulsant therapy for Acute Symptomatic Seizures in Children with Acute Encephalitis Syndrome?
Sumeet Rajendra Dhawan, Jitendra Kumar Sahu, Pratibha Singhi, Naveen Sankhyan, Jayashree Murlidharan
ENTEROVIRUSES NEUROINFECTIONS IN CHILDREN IN UZBEKISTAN.
Abrorjon Khoshimov
Enzymatic changes in the CSF in children with neuroinfections in uzbekistan.
Makhmudjon Bakhromov
Herpes encephalitis at children in Uzbekistan.
Makhmudjon Bakhromov

Education and Training

PEDIATRIC NEUROLOGY SERVICES IN RURAL MAHARASHTRA, INDIA AN 8 YEAR TREND
Anaita Udwadia Hegde, Roshan Kore, Purva Keni Karnavat, Asha Chitnis, Snehal Deshpande, Chetna Bhatt, Gayatri Hattiangadi, Nitin Nirmal, Sachin Pingale
The Quality of Life (QoL) in Indian Children with Learning Disorders – a case control study
lekha mishra
Closing the Epilepsy Treatment Gap: A Pediatric Epilepsy Education Initiative for Primary Care Providers in Zambia
Leah Wibecan, Ornella Ciccone, Owen Tembo, Prisca Kalyelye, Manoj Mathews, Archana A. Patel
Worldwide short course education programmes in epilepsy for paediatricians – are they effective?
Alison Gifford, Jo Wilmshurst, Finbar O'Callaghan, Mike Griffiths, Colin Dunkley, Philippa Rodie, Helen Cross, Martin Kirkpatrick
Flipped classroom versus traditional lecture in training undergraduate medical students on pediatric epilepsy: A randomized controlled trial
Jaya Shankar Kaushik, Vandana Arya, Radhamohan Rana, Anjali Verma, Harish Bhardwaj
Experience in providing a short training on EEG recording technique and reviewing in Bangladesh, Tanzania and Ghana
SELINA HUSNA BANU, Naila Zaman KHAN

Development Cognition and Psychiatry

Gratification phenomena in infancy: a report of twenty-nine children.
ROSHAN KOUL
Predictors of intellectual abilities among children with autism spectrum disorder
Watfa Al-Mamari, Ahmed Babiker Idris, Ahlam Ali Abdelsattar, Abeer Al-Mujaini, Muna Al-Jabri
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India
shriganesh patil, Abhinav Neela, Arpita Thakker, Smita Patil, Nandkishor Jadhav, Mona Gajre
The Assessment and Management of Childhood Masturbation: An Analysis of 45 Cases
Hüseyin Per
Near-infrared spectroscopy (NIRS) based neurofeedback training in children with Tourette syndrome(TS)
Pou-Leng Cheong, Chia-Wei Sun
ROLE OF LINGUISTIC PROFILING INASSESSMENTS OF LEARNING AND LANGUAGE DISORDERS IN INDIAN CHILDREN-A CASE CONTROL STUDY
MsNitya Raman, Dr Mona Gajre, DrNandini Singh
A NON LINEAR DYNAMIC AYURVEDA APPROACH FOR THE MANAGEMENT OF CHILDREN WITH AUTISM SPECTRUM DISORDER
DINESH KS, RAJESH N, JAYADEVAN CV, GEORGE MJ, ANITA PATEL
The sensory processing patterns of children with Autism Spectrum Disorder: Impact on behavior problems and adaptive behavior
MUTHUVEL RAJANGAM
To test if separation anxiety(SA) is absent/attenuated in autistic children
Nisreen Hussain Bohra
The Quality of Life (QoL) in Indian Children with Learning Disorders – a case control study
lekha mishra, jagruti bawa, smita patil, arpita thakker, manikantan r, mona gajre
Tuberous Sclerosis Complex (TSC)-Associated Neuropsychiatric Disorders (TAND): New Findings on Age, Gender and Genotype in Relation to Intellectual Phenotype
Petrus J De Vries, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood, Anna C Jansen
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India
shriganesh patil
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India
shriganesh patil, Abhinav Neela, Arpita Thakker
PROFILE OF CHILDREN WITH AUTISTIC SPECTRUM DISORDER ATTENDING A PUBLIC HEALTH HOSPITAL-AN INDIA EXPERIENCE
Dr Vidya Manjeri, Ms preeti Gurav, Ms Bhakti Anant Vanmali, Dr Sushant Sarang, Dr Avinash Dsouza, Dr Mona P Gajre
A STUDY ON HEAVY METALS PROFILE IN CHILDREN WITH AUTISM
Mogili Sudha Priyanka, SAVITA VERMA ATTRI, PRATIBHA SINGHI, PRAHBHJOT MALHI, JITENDRA KUMAR SAHU, ARUSHI GAHLOT SAINI
Creating an assessment scale of social and behavioral development for preschool children -The process of creating the scale-
Hideyo Goma, Shun Tanaka, Michio Ushiyama, Tomomi Ikeda, Rika Ochiai, Toshihiro Kato, Satomi Shimizu, Kazuhisa Inoue, Reiko Ushio, Hiromi Kotani
Cognitive visual dysfunctions in children with autism spectrum disorders and other developmental disabilities
Eu Gene Park, Young Hoon Kim
“Prevalence of Autism spectrum disorders (ASD) in a latinamerican city, first epidemilogical study in children 18 – 36 months of age”
Francisco Alberto Astorino, Elena Carrera, Liliana Contini
Effect of a Combination of Carnitine, Coenzyme Q10 and Alpha-Lipoic Acid (MitoCocktail) on Mitochondrial Function and Neurobehavioral Performance in Children with Autism Spectrum Disorder
Agustin Legido, Michael Goldenthal, Brigid Garvin, Shirish Damle, Kelleen Corrigan, James Connell, Diana Thao, Ignacio Valencia, Joseph Melvin, Divya Subramanian Khurana, Mitzie Grant, Craig Newschaffer
PREVALENCE AND CLINICAL CHARACTERISTICS OF AUTISM SPECTRUM DISORDER AT A TERTIARY HOSPITAL IN ZAMBIA
Kafula Lisa Nkole, Ornella Ciccone
The Effect of Glucocorticoid Receptor (GR) Function on the Behavior of ADHD Rats and the Mechanism of Interaction between GR and MAO A
Yanhui Chen, Hongzhu Lu, Jun Hu, Xiaoxia Lin
To address the issue comprehensively by measuring various neurobiological parameters exclusively in children and adolescents and an effort to bridge the gap between childhood and adult aggressive behavior.
P K Maheshwari, Sagar Lavania, Vishwas K
Neurodevelopmental Outcome After Neonatal Hypoglycemic Brain Injury .
Madhavi Shelke, Abhay Jain, Madhura Anvikar, Pratima weldode, Abdul Muqueet
Parental use of rehabilitation services and complementary therapy for autism in Jordan
amira masri
ROLE OF LINGUISTIC PROFILING INASSESSMENTS OF LEARNING AND LANGUAGE DISORDERS IN INDIAN CHILDREN-A CASE CONTROL STUDY
Nitya Raman, MONA GAJRE, DrNandini Singh
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India
shriganesh patil, Abhinav Neela, Arpita Thakker, Smita Patil, Nandkishor Jadhav, Mona Gajre
Tele medicine via Video Consultations for children awaiting Developmental Assessement
Edith Posener
All work and no play: The relationship of leisure time activities and psychological disorders in school children
Pallavi Bhad, Gouri Rao Passi
Vitamin B12 status and Neurodevelopmental delay in Infants in Northern India
Chandrika Azad
Eating behaviour in Children with Autism
Sachitra Rathod, Subramanian Mahadevan
Plasma amino acid profile in children with autism spectrum disorder
Wen-Xiong Chen, Min-Zhi PENG, Yan-Na CAI, Zhi-Fang HUANG, Jin-Yu HUANG, Si-Yuan YANG, Peng YI, Li LIU
Acupuncture for non-verbal autistic children: a randomized controlled trial
Wen-Xiong Chen, Gang LIU, Hong-Sheng LIU, Zhi-Fang HUANG, Jin-Yu HUANG, Si-Yuan YANG
18 F- FDG PET scan abnormalities at rest in children with Autism Spectrum Disorder
Razia A Kadwa, Pratibha D Singhi, Prahbhjot Malhi, Jitendra K Sahu, Naveen Sankhyan, Mittal B.R, Rajinder K
Pseudospasticity dysbasya in children
Julia Sadovskaya, Valentina Rodionova, Maria Karpilova, Anna Bitova
The Clinical Profile of epilepsy and electroencephalographic abnormalities in Children with Autistic Spectrum Disorder – A Retrospective Study
ALPANA SANTOSH KONDEKAR, Sandeep Bavdekar
PSYCHIATRIC CO-MORBIDITIES IN CHILDREN WITH AUTISM SPECTRUM DISORDERS
Somini Haresh Mehta, Neelu Desai
To study correlation of social emotional and communication scores based on Development profile 3 test and the Childhood Autism Rating Scale ( CARS) scores in children fulfilling the DSM V criteria for Autism Spectrum disorder.
Shambhavi Seth, Satinder Walia, Zeba Parveen
Efficacy of Weighted Compression Vest on Hyperactivity, Inattention and Core Symptoms in children with Autism Spectrum Disorder: an interventional pilot study
Nishtha Gupta, Deepti Gupta, Aparajita Gupta, Shobha Sharma, Lokesh Saini, Prateek Kumar Panda, Asha Chitnise, Sheffali Gulati
Health related Quality of Life in Children with Autism Spectrum Disorder aged 3-12 years and correlation with severity of autism and behavioral co-morbidities: a cross-sectional study
Prateek Kumar Panda, Sheffali Gulati, Sanjeeda Khan, Shobha Sharma, Priyanka Madaan, Bhavya G, Prashant Jauhari, R M Pandey
Spectrum of Genetic Etiologies in children with Autism Spectrum Disorder: a single institution observational study
Sheffali Gulati, Prateek Kumar Panda, Priyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty, Aparajita Gupta, Ankita Pal, Sachendra Badal, Vishal Sondhi, Neerja Gupta, Madhulika Kabra
A Mobile Autism Risk Initiative (AMARI) to Detect Autism Spectrum Disorder in Bangladeshi Children Under the Age of 4
Dennis P Wall
Analysis of outcomes of an interdisciplinary developmental program for syndromic children with neurological deficits
DIPTI KHOPKAR, SAMIR DALWAI
Neurodevelopmental disease pattern in a tertiary care hospital-An experience in Bangladesh.
BISWAJIT CHOWDHURY
Comparison of blood heavy metal levels in children with Autism Spectrum Disorder aged 3-12 years and typically developing children: A cross sectional study
Sheffali Gulati, Aparajita Gupta, Shobha Sharma, Prateek Kumar Panda, Biswaroop Chakrabarty, Rachna Sehgal, Amita Srivastava, Y K Gupta, R M Pandey
Comparison of Executive Function between children with Autism Spectrum Disorder and Typically Developing Children: a Cross-sectional study
Ratna Sharma, Asfa Ahmad, Shobha Sharma, Prateek Kumar Panda, Aparajita Gupta, Rupesh Samanchi, Sana Sayeed, Prashant Jauhari, Biswaroop Chakrabarty, Sheffali Gulati
Nutritional Status of Children with Autistic Spectrum Disorder
Dr. Vidya Manjeri, Priya Karkera, Disha Bagadia, Bhakti Anant Vanmali, Dr. Sushant Sarang, Dr. Avinash Dsouza, Dr. Mona P. Gajre
Clinical Spectrum and Management Outcome of Psychogenic Non Epileptic Seizures in Children: A Prospective Observational Study
Sheffali Gulati, Shobha Sharma, Prateek Kumar Panda, Priyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty
Cognitive Functioning in Children with Epilepsy: Generalized Seizures (GS), Complex Partial Seizure (CPS) and Temporal Lobe Epilepsy (TLE)
Gopukumar Kumarpillai, Sree Krupa Manthri, ashwini S Kalkunte, Umashankar R, shobha Nandavar, Girish Gadre, Murthi G
NON PHARMACOLOGICAL PROTOCOL FOR TREATING ADHD CHILDREN (NFB,CES,CCT)
hussein hosny abdeldayem
Mobile Media Use in Children with a Neurodevelopmental Disorder from the ages of 0-8years.
Franzina Coutinho, Akansha Shah, Shantanu Tilak, Neelu Desai, Vrajesh Udani
Use Of mobile media among children (0-8years) with ASD against the typically developing control group
Franzina Coutinho, Akansha Shah, Shantanu Tilak, Neelu Desai, Vrajesh Udani
Prevalence of internet gaming disorder in patients in the age group 5-12 years presenting to the outpatient department of a tertiary care hospital in Delhi
Meenakshi Bhatt, Rachna Sehgal, Aditi Tiwari
Can specific EEG criteria contribute as a neural marker for the siblings of Autistic children?
Razia Sultana
NEUROCOGNTIVE OUTCOMES IN SURVIVORS OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA
Vishwa CR, Rachna Seth
The Perturbance of Microbiome and Gut Brain Axis in Autism Spectrum Disorders
Sue Xue Ming
INFLUENCE OF SENSORY INTEGRATION OCCUPATIONAL THERAPY IN REDUCING NEGATIVE BEHAVIOR 2 TO 5 YEARS CHILDREN WITH AUTISM SPECTRUM DISORDERS
Junita Elvira, Hardiono D Pusponegoro, Setyo Handryastuti
Rare diseases presenting with Autism Spectrum Disorder (ASD); An etiological conundrum
Vrushabh Sopan Gavali, Leena Srivastava, Nirali Thakker, Sujit Jagtap
Association between Sleep Disturbances and Sensory-over-responsivity in Children with Autism Spectrum Disorder.
Akansha Shah, Somini Mehta, Neelu Desai, Vrajesh udani
A Study of Trace Elements Status in Children with Infantile Tremor Syndrome: An Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) Based Study
Trinity Deepak Francis
EVALUATION OF HYPERANDROGENISM IN CHILDREN WITH AUTISM SPECTRUM DISORDER AND AGE-SEX MATCHED CONTROLS
Neeharika Sriram
EVALUATION OF HYPERANDROGENISM IN CHILDREN WITH AUTISM SPECTRUM DISORDER AND AGE-SEX MATCHED CONTROLS
Neeharika Sriram, Jitendra Kumar Sahu
Children's Pathology Leading to Disruption of Object Relations
Umesh Jain
The effect of omitting breakfast on cognitive function and blood glucose level among adolescent secondary school students
Halima Adamu
Targeted gene sequencing in children with autism spectrum disorder
Mary Iype, Anitha Ayyappan, PA SURESH
AUTISM - Is there an increased risk from ART (artificial reproductive technique)
Darshana N Vora, Nitish S Vora
Demographic details of children with Autism presenting to a specialist Autism center
Darshana N Vora, Nitish S Vora
Early Detection of Developmental Problems by Parents
Sundara sabaratnam Sam LINGAM
Diagnostic Investigations of Children with Learning Difficulties
Sundara sabaratnam Sam LINGAM
Magnitude of sleep problem in children with Neurological disorders compared with normal population
Darshana N Vora, Nitish S Vora
Cranial neuroimaging findings in nutritional vitamin B12 deficiency (NVBD) in infants
Jatinder Singh Goraya
Picky Eating in Autism Spectrum Disorder, its Characters and Treatment
Shigeru Hanaoka
Autism and ADHD: Differential functioning on a Computerized Performance Test (MOXO-CPT)
YAEL LEITNER
STRUCTURE OF SLEEP IN CHILDREN WITH EPILEPSY AND COGNITIVE IMPAIRMENT.
Abrorjon Khoshimov
Shared atypical functional connectivity in children with autism spectrum disorder and attention- deficit/hyperactivity disorder
EVDOKIA ANAGNOSTOU
A Phase 2 Randomized, Placebo-Controlled Trial of Tideglusib, an Orally Administered GSK3Beta Inhibitor, in the Treatment of Adolescents with Autism Spectrum Disorder
EVDOKIA ANAGNOSTOU

Epilepsy

Evaluation of vitamin B12 levels in children with Infantile spasms and children with Global Developmental Delay without Infantile spasms: A cross sectional observational study
Mahender Kumar Meena
EEG services for children in Africa: Pilot survey of capacity and needs
Veena Kander
Febrile Infection Related Epilepsy Syndrome (FIRES) - A multi-centric study from India
Sandeep Bhagwan Patil, Neha Manjhani, Rakhi Sharma, Ravi Sharma, KP Vinayan, Arun Grace Roy, Vivek Jain
Practical aspects of the use of Ketogenic Diet in the management of Childhood Epilepsy- a review of experience from Scotland
Elma Stephen, Lucy Elphinstone, Helen Grossi, Tracy Cameron
Efficacy of Modified Atkins Diet (MAD) as Treatment for Intractable Epilepsy in Children - A Randomized Controlled Trial.
Nazmul Haque
Assessment of Oral Hygiene of Children with Epilepsy
Mohammed M Jan
Clinical Profile and Outcomes of Epilepsy surgery in children from tertiary epilepsy care center India
Sandeep Bhagwan Patil, Nilesh Kurwale, Sujit Jagtap
Treatment approach for neonates with acute symptomatic seizures influences length of hospital stay
Hannah C. Glass
Levels of Immunoglobulins, Complement and T Lymphocyte Subsets in the Peripheral Blood of Children with Convulsive Diseases and Their Signifiances
XY GUO
Plasma Galanin and Neuropeptide Y Levels in Children with Convulsive Diseases and Their Signifiances
XY GUO
Classifying Electroencephalographic Diagnoses of Epilepsy without Epileptiform Discharges and Nonepileptic Paroxysmal Events Using Deep Convolutional Neural Networks
Lung-Chang Lin, Chen-Sen Ouyang, Ching-Tai Chiang, Rong-Ching Wu, Hui-Chuan Wu, Rei-Cheng Yang
The clinical efficacy and follow-up study of ketogenic diet adding treatment for refractor epilepsy in children
Zeshu Ning
TITLE: PAROXYSMAL NON-EPILEPTIC EVENTS IN A PEDIATRIC EPILEPSY CLINIC: A PROSPECTIVE STUDY
Neelu desai
The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE)
Sun Dan
Canonical transient receptor potential chan nel 3 contributes to recurrent febrile seizure s by inducing neuronal cell death and neuroi nflammation
Sun Dan
Study of 15 patients with early infantile epileptic encephalopathy -treatable Neurometabolic causes
harshuti biren shah
Factors associated with Electroencephalographic and Clinical Remission of Benign Childhood Epilepsy with Centrotemporal Spikes
Su Jeong You, Eun Hye Lee
GABA TRANSAMINASE DEFICIENCY DISORDER IN AN INDIAN FAMILY - REPORT OF TWO NEW CASES
Ruchita Vyas, Omkar Hajirnis, Purva Keni Karnavat, Anaita Udwadia Hegde
KETOGENIC DIET: DO WE NEED 4:1 RATIO FOR KETOSIS?
Purva Keni Karnavat, Anaita Udwadia Hegde, Shilpa Kulkarni, Roshan Kore, Bhakti Tulaskar, Suvarna Sawant
Epilepsy Genetics – a new weapon in our Armamentarium!
Dr Tarishi Nemani, Dr Vishal Kanubhai Patel, Dr Purva Keni Karnavat, Dr Anaita Udwadia Hegde
Clinical features and efficiency of ketogenic diet of 106 Dravet syndrome patients
JING PENG
Analysis of clinical and genetic features of 30 patients with KCNQ2-related disorder
JING PENG
CLINICO-ETIOLOGICAL PROFILE OF REFRACTORY STATUS EPILEPTICUS IN CHILDREN
KC Sadik, Devendra Mishra, Urmila Jhamb, Monica Juneja
Electroencephalogram Features of Children with Type 1 Diabetes Mellitus
Ceren Gunbey, Ruken Yıldırım
Perampanel and Brivaracetam: Efficacy and safety in pediatric refractory epilepsy
Divya Subramanian Khurana, Ana Melikishvili, Sara McGuire, Karen S Carvalho, Ignacio Valencia, Daphne M Hasbani, Uzma Sharif, Agustin Legido
Intravenous Fosphenytoin loading dose of 20 mg/kg in Status epilepticus: Is it enough in Indian children?
Kavita Srivastava
It’s not all about seizures: Experience of Dravet Syndrome management in a Scottish Children’s Hospital
Sylvia Yuk San Tran, Elma Stephen
First Complex Febrile Seizure – do we need to investigate.
Arpita Devbrata Adhikari, Krishna Shetye, Smita Patil, Mona Gajre
Prevalence of Epilepsy and Inter-ictal Epileptiform discharges in children with Neurodevelopmental disorders
B Anukirthiga, Devendra Mishra, Sanjay Pandey, Monica Juneja
Seizures in children with Zika Virus Congenital Syndrome
Lucas Victor Alves, Patrícia Gomes de Matos Bezerra, Maria Júlia Gonçalves de Mello, Ana Rodrigues Falbo, José Natal Figueiroa
A critical analysis of lumbar puncture in the emergency management of febrile seizures: a cross-sectional study
Eduardo Jorge da Fonseca Lima, Gabriel Brito de Moura Monteiro, Alberto de Barros Lima Filho, Lucas Victor Alves
Clinico-etiological Profile and Developmental Status of Infants Aged 1-24 months with Epilepsy in India
Pankaj Kumar Sahu, Devendra Mishra, Monica Juneja
Ohtahara Syndrome due to unique Heterozygous PIGO mutation: Clinical and EEG features
Arayamparambil C Anilkumar
Congenital Mirror Movements with epilepsy in association with KCNT1 gene mutation: A Case Report.
RAGHAVENDRA K
National Surveillance of Mortality in Children with Epilepsy in the UK and Ireland
Omar Abdel-mannan, Alastair Sutcliffe
The absence of NIPA2 enhances neural excitability through BK channels
Han Xie, Nana Liu, Wenshu Xiangwei, Kai Gao, Tianshuang Wang, Yuwu Jiang
Pediatric status epilepticus. Cases admitted during years 2015-2016 at Hospital de niños Dr. O. Alassia de la ciudad de Santa Fe, Argentina.
Francisco Alberto Astorino, Betiana Comas, María Inés Malatini
Efficacy of adjunctive vagus nerve stimulation in patients with Dravet syndrome
Songee Youn
Evolution of epileptic zeisures iniciated during neonatal period in a long term follow up of 97 children
Francisco Alberto Astorino, María Ines Malatini, Betiana Comas
Febril status epilepticus in children. Series of cases of children admited at Dr. O Alassia Hospital, Santa Fe Argentina period 2015 to 2018
Francisco Alberto Astorino, Betiana Comas, María Inés Malatini
Absence epilepsy, the great masquerader
Samata Singhi
Not all that blinks is tics
Samata Singhi
Epileptic Spasms in Southern Africa
Sharika V Raga
Autoimmunity of childhood epilepsy
sonali verma, Anju Aggarwal, Gargi Rai, Shukla Das
KETOGENIC DIET IN ZAMBIA: MANAGING REFRACTORY EPILEPSY IN A LOW INCOME COUNTRY.
Kafula Lisa Nkole, Nfwama Kawatu, Chimbizyani Kanyinji, Theresa Njobvu, Ornella Ciccone, Stacey Tarrant, Archana A Patel, Annmarie Bergin
Open label randomized comparison of levetiracetam and sodium valproate monotherapy in childhood epilepsy
SWATI BHAYANA
Hemimegalencephaly with congenital facial lipoma-A Case Report
Subramanian Velusamy, Subramanian Velusamy, Balaraman Krishnakumar
The efficacy and safety of levetiracetam treating in pediatric epilepsy in different ages and seizure types
Yu Liu, Xueying Wang, Gaobo Ye, Shaoping Huang, Lin Yang
A Chinese boy with Malonyl-CoA decarboxylase deficiency and a novel mutation in the MLYCD gene
Fang Wang, Lin Yang
Nurse Lead “Multi Levels” Pediatric Epilepsy Education Initiatives
Amal Chaman Chehab
Experience with very high dose (8mg/kg/day, maximum 60mg/day) prednisolone for West syndrome in a resource limited setting
Sunil Malik
Comparison Of Electroencephalographic Sleep Stages With Bispectral İndex Data İn Children
Sanem Yılmaz, Hasan Tekgul, Erdem Simsek, Hande Tekin, Hepsen Mine SERIN, Gul Aktan, Sarenur Gokben
Effects of ketogenic diet on plasma levels of valproic acid in children with epilepsy
Fang Wang, Jinqiu Wang, Baoni Mu, Lin Yang
Cannabinoid receptor type 2 controls neuronal autophagy through regulation of mTOR signal pathway during the repair of hippocampal neurons in status epilepticus rats
Qiong Wu, Hua Wang
Comparison of Epileptic Seizure Classifications (ILAE-1981 and ILAE-2017) with A Modular Education Program Among Residents in Pediatrics
Meherrem Imanli, Hasan Tekgul, Erdem Simsek, Hepsen Mine Serin, Seda Kanmaz, Sanem Yilmaz, Gul Aktan, Sarenur Gokben
Tuberous Sclerosis Complex (TSC) - Associated Epilepsy: Final Results from the TOSCA Study
Rima Nabbout, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, Petrus J De Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, Anna C Jansen, John C Kingswood
Perampanel in paediatric population: experience in a regional hospital
Nikole Ada Tracy, Wing Cheong Lee, Li Yan Tsung, Shuk Mui Tai, Kam Tim Liu
Risk Of Recurrence After Withdrawal Of Antiepileptic Medication In Children With Epilepsy
Mizanur Rahman, Sufia Khatun Sumi, Kanij Fatema
WWOX related epileptic encephalopathy: A new autosomal recessively inherited disorder
Hepsen Mine SERIN, Gurkan Gurbuz, Betul Kilic, Bulent Kara, Sarenur Gokben
Analysis of curative effect and  influence factors of small dose and short course of ACTH on 73 cases of IS
Xiaodi Han, Fang Fang, Chunhong Chen
Clinical and EEG characteristics of epilepsy of infancy with migrating focal seizures
Shuqian Zhang, Ruopeng Sun, Baomin Li
De novo Mutation among a Chinese Infantile Spasms Cohort and Precision Treatment with Levetiracetam in Four de novo STXBP1 Mutation Patients
Li-ying Liu, Fang Liu, Yang-yang Wang, Gui-Xia Zhang, Meng-Na Zhang, Qian Lu, Li-Ping Zou, Xiao-Li Chen
The value of mobile phone videos in increasing the diagnosis accuracy and saving cost of consultation for infant paroxysmal events: a prospective study in China
Lu-Lu Huang, Yang-Yang Wang, Li-Ying Liu, Hong-Ping Tang, Meng-Na Zhang, Shu-Fang Ma, Li-Ping Zou
Establishment and utility assessment of Posterior Reversible Encephalopathy Syndrome early warning scoring (PEWS) scale Establishment and utility assessment of PEWS scale
Li-Ping Zou, Hui Li, Li-ying Liu, Yang-yang Wang, Ying Liu, Jing Chen, Lin-Yan Hu, Meng-Jia Liu, Meng-Na Zhang, Shu-Fang Ma
First unprovoked seizure in children-Predictors of recurrence
Smita Prabhakar Patil
Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation
ChunHong Chen, HuSheng Wu, XiaoHui Wang, HongMei Wang, XiaoTun Ren, JunLan Lv, Fang Fang
Adverse drug reactions of anti-epileptics in children-an observational studySundeep Kaushik, Suvasini Sharma, Deepti Chopra, Bijoy Patra, Satinder Aneja
Dr Sundeep Kaushik
The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE).
Liu Zhi Sheng
A unique variant of West Syndrome:Vitamin B12 responsive epileptic encephalopathy
Harshkumar Arvindbhai Patel, Prarthana Kharod, Prarthana Kharod
Clinical profile and short-term outcome of status epilepticus in children
Chinmay Chetan, Satinder Aneja, Suvasini Sharma, Bijoy Patra, Surendra Bahadur Mathur
Accelerated corticospinal tract maturation, as measured by neuronavigated transcranial magnetic stimulation (nTMS), corresponds to preserved IQ in girls, but not in boys, with focal epilepsy
Harper Lee Kaye, Clemente Vega, Ali Jannati, Melanie McNally, Gabrielle Block, Alvaro Pascual-Leone, Alexander Rotenberg
SYNDROMES AND ETIOLOGY IN PEDIATRIC EPILEPSY: EVALUATION OF INTERNATIONAL LEAGUE AGAINST EPILEPSY (ILAE) 1989, 2010 AND 2017 CLASSIFICATION OF EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, satinder aneja
FEATURES OF EPILEPSY AND CEREBRAL PALSY IN CHILDREN IN UZBEKISTAN.
Abrorjon Khoshimov
DESCRIPTIVE EPIDEMIOLOGY OF “CONTINUOUS SPIKE AND SLOW WAVE IN SLEEP (CSWS)” EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, Satinder Aneja
Clinico-Etiological profile of acute seizures in children admitted in PICU and their short-term outcome
Suman Choudhary, DR SWATI MULYE, DR GUNJAN KELA MEHROTRA, DR CHANDAN KUMAR SHAW
Profile of children with seizures and epilepsy presenting at a tertiary care specialist Paediatric epilepsy clinic
Nitish S Vora
ELECTROCLINICAL PROFILES OF CHILDREN WITH BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES (BECTS) AT A TERTIARY CARE CENTRE
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, Satinder Aneja
PROFILE OF CHILDHOOD EPILEPSY AT A TERTIARY CARE HOSPITAL IN SOUTHERN INDIA Janani R1,Saji James2,Ranjith Kumar 3 ,1Post graduate,2 Professor of Pediatrics,Department of Pediatrics,3 Assistant Professor Paediatric neurology Sri Ramachandra medical college
Janani Raghunathan
Lacosamide responsive ESES (electrical status epilepticus in slow wave sleep )– 2 case reports
pradnya gadgil, Nilima Bhalerao, Sunita Venkatraman
‘Prevent Neonatal hypoglycaemia, Prevent Infantile Spasms: Revealing findings from an etiological study on West Syndrome patients from North India
Prabhar Srivastava, Priyanka Surana, Romit Jain, Vedam Ramprasad, Thenral SG, Sakthivel Murugan, Vivek Jain
A clinical and electrophysiological profile of epileptic spasms- A tertiary care centre experience
abhishek ravindra jain, mary iype, P A Mohammed Kunju, mini sreedharan, bindu thankappan
A Practical Quality of Life Questionnaire for Children with Severe Intellectual Disability and Epilepsy: Comparing proxy reporting by Mothers and Fathers
Vivek Mundada, Deepak Parashar, APJ Parker
Effectiveness and tolerability of perampanel in children under 7 years old with refractory epilepsy: A single-center, retrospective study
Fu-Man Chang, Wen-Chin Weng, Pi-Chuan Fan, Wang-Tso Lee
A NEW VEGETATIVE SIGN RELATED TO ANTERIOR INSULA EPILEPSY: IPSILATERAL “GLOVE AND SOCK” SKIN CYANOSIS
Oana Tarta-Arsene, Oana Tarta-Arsene, Sergiu Stoica, Sergiu Stoica, Sorin Tarnoveanu, Diana Gabriela Barca, Sorin Tarnoveanu
A case of KCNA2 encephalopathy presenting with various involuntary movements, severe psychomotor retardation, and sleep disturbance.
Tatsuharu Sato
Infantile epilepsy with prolonged focal myoclonic seizures: A distinctive syndrome associated with TBC1D24 mutation.
Deepa Sirsi, John Schreiber, Satish Agadi, Robert S Greenwood, Susan T Arnold
Status Epilepticus in Pediatric Patients Severity Score (STEPSS): A clinical score to predict the outcome of status epilepticus in children.
Sidharth Yadav, Suvasini Sharma, Bijoy Patra, Rajeev Malhotra, Virendra Kumar
Screening for Mental Health Problems in Children and Young People with Epilepsy and Early Management in the Clinic Setting
Ailsa McLellan, Suzanne Felix, Catriona George, Kirsten Verity, Michelle Small, Celia Brand, Richard Chin, Jay Shetty
What to expect from an unexpected seizure?
Rosa Lualdi, Giulia Bravar, Valentina Dolcemascolo, Paola Cogo, Giovanni Crichiutti
THE CLINICAL CASE OF EPILEPTIC ENCEPHALOPATHY IN ANGELMAN SYNDROME.
Akmal Asatullayevic Mukhamedov
Clinico-radiological and electrographic spectrum of children with Temporal lobe epilepsy: a retrospective cohort study
Zulfiqar Luhar, Biswaroop Chakrabarty, Ankita Pal, Prashant Jauhari, Atin Kumar, Shobha Sharma, Sheffali Gulati
Outcome of Rasmussen Encephalitis with conservative management
Bijoy Patra, Surendra Bahadur Mathur, Kanti Lal Chakraborti, Preeti Gaddad, Suvasini Sharma, Satinder Aneja
Clinical and Molecular profile of First Indian cohort of Unclassified West Syndrome Patients
Romit Jain, Priyanka Surana, Prabhar Srivastava, Thenral SG, Ramprasad V, Saktivel Murugan, Subathra Mahalingam, Aishwarya Subramaniyan, Sameer M Zuberi, Vivek Jain
Microbiological diagnostic challenges in a seasonal cluster of Rhombencephalitis
smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Milind Shah, Srikanth Domala, Ashwini Mohan, Ravi verma
Achievement of camp in children with epilepsy
Monika Kukuruzovic, Masa Malenica, Iva Separovic, Kristna Kuznik
ETIOLOGICAL CLASSIFICATION (ILAE-2017) AND THERAPEUTIC REPONSE IN CHILDREN WITH EPILEPSY PRESENTING AT A TERTIARY CARE SPECIALIST EPILEPSY CLINIC.
Nitish S Vora
Hemiconvulsion Hemiplegia Epilepsy Syndrome: A case Report
DEEPAK DWIVEDI, Chitra soni, jyoti singh
Prolonged Seizures in Children
Clodagh Mitchell, Jay Shetty, Libby Dickson, Celia Brand, Paul Leonard, Ailsa McLellan
Study of Drug Resistant Epilepsy at a Tertiary Care Centre in Western India 2018
Rasika Sandeep Bharaswadkar
Pediatric lamotrigine overdose resulting in generalized seizure and encephalopathy
Djurdja Djordjevic
Prevalence and association of risk factors for anticonvulsant polytherapy amongst epileptic children: A case-control study
Shifa Bidhan, Krishna M Adhikari, Rakesh Kumar Gupta
Improving triaging of Infantile Spasm EEG referrals in a large Canadian institution
Djurdja Djordjevic
A case of De Novo NAA10 mutation presenting with eyelid myoclonias (AKA Jeavons syndrome)
Vinod Valentine
Parietal epilepsy presenting as eye flutter and absences
Kalyani Dilip Karkare
Significance of polyspikes on electroencephalogram in children with focal epilepsy
Ara Ko, Ju Hyun Kong, Yun-Jin Lee, Sang Ook Nam
Experience of ketogenic diet as an adjuvant therapy in Febrile Infection Related Epilepsy Syndrome (FIRES)
Purnima Suhas Prabhu, Vrajesh Udani, Toral Bhatt, Neelu Desai
Ketogenic Diet (KD) in children with epilepsy: Parental expectations and experiences
Rajesh RamachandranNair, Nandini Nandeesha
The role of sleep and awake EEGs in detection of epileptiform discharges in pediatric population.
Nupur Sinha, Shilpa Kulkarni, Suresh Birajdar, Tushar Maniar
ketogenic diet in infant with intractable epilepsy
alifiani hikmah putranti
Evolution and Outcome of Epilepsy in Children with Neonatal Hypoglycemic Brain Injury
Neeta Ajit Naik
Clinical utility of next generation sequencing in Early-Onset Epileptic Encephalopathies
Vishal Sondhi, K M Adhikari, Vishal Vishnu Tewari, K Venkatnarayan, Rakesh Gupta
Genotype and phenotype of epileptic patients with SCN2A mutations
Qi Zeng, Xiaoling Yang, Dan Wang, Jing Zhang, Jiaoyang Chen, Aijie Liu, Xiaoyan Liu, Xiru Wu, Yuwu Jiang, Yuehua Zhang
Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations
Jing Zhang, Jiaoyang Chen, Qi Zeng, Liping Zhang, Xiaojuan Tian, Xiaoling Yang, Zhixian Yang, Ye Wu, Yuehua Zhang
Hypothyroidism and valproate: Is there a causal relationship?
Chhitiz Anand
Epilepsy Versus Chronic diseases: How different are parent’s attitudes?
Noha El tantawi, Dina Abd Elmegid, Eman Atef
The electroclinical features of CHD2 mutation related epilepsy
Jiaoyang Chen, Jing Zhang, Qi Zeng, Liping Zhang, Hua Li, Zhixian Yang, Xiaoling Yang, Aijie Liu, Yuehua Zhang
Electrophysiological characteristics in children with Subacute sclerosing panencephalitis (SSPE): A study from a tertiary care hospital.
ANSHITA ARORA, SHILPA KULKARNI, MEENAL GARG, SONAM KOTHARI, ANAITA HEGDE, KRISHANKUMAR SHAH
CLINICOETIOLOGICAL PROFILE OF CHILDHOOD SEIZURES IN A TERTIARY CARE HOSPITAL: A PROSPECTIVE OBSERVATIONAL STUDY
Akash Rai, Dipankar Gupta, Sankar Kumar Das
Up-regulation of HMGB1-TLR4 Inflammatory Pathway in Focal Cortical Dysplasia Type II
Ye Wu
Super Refractory Status Epilepticus in children : Etiological, electrophysiological, treatment and outcome profile
Deepti Ashok Kewalramani, Sonam Kothari, Shilpa Kulkarni, Anaita Hegde, Krishankumar Shah
Does Ethnicity Affect the Clinical Presentation of Tuberous Sclerosis Complex?
Ravi Benjamin Dhamija, Cigdem Akman, Aliza Alter, Daniel McBrian, Elena Gonzalez
Serum levels of both prolidase activity and oxidative stress in epileptic children
Nurettin KARACAN, Mustafa CALIK
Role of Arterial Spin Labeling (ASL) in Localization of Epileptogenic Focus for Pre-surgical Evaluation of Intractable Epilepsy.
Rahul M Nikam, Vinay Kandula, Arabinda Choudhary, Harry Chugani
Functional Hemispherotomy : patient characteristics and outcome in a series of 26 patients
Lakshminarayanan Kannan, Dinesh Nayak, Ravi Mohan Rao
Clinical characteristics and epilepsy outcomes after surgery in children with focal cortical dysplasia type II
tianshuang wang, Ming Liu, Jie Zhang, Lixin Cai, Qingzhu Liu, Yuwu Jiang, Ye Wu
Semiological, Diagnostic and theraupetic challenges in Infantile onset epilepsy
Smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Shah, Srikanth Domala, Prasanthi Aripirala, Ravi verma
KNOWLEDGE ATTITUDE PRACTICE (KAP) STUDY FOR THE CARE OF CHILDREN WITH EPILEPSY IN SCHOOLS
Darshana N Vora, Nitish S Vora
Hemispherotomy for catastrophic epilepsy: our early experience
Sujit Abajirao Jagtap, Nilesh Kurwale, SANDEEP PATIL, SONAL CHITNIS, ANIRUDHA JOSHI, SUJIT NILEGAONKAR
Vagal Nerve Stimulation treatment in children with pharmaco-resistant epilepsy: A single centre experience
Mazen Haider, Helen McCullagh, Gayatri Vadlamani, Janet Kellett, Gopalakrishnan Venkatachalam
Clinical profile of patients with infantile spasms following Neonatal hypoglycemic brain injury: a retrospective study from India
Romit Jain, Prabhar Srivastava, Priyanka Surana, Vivek Jain
Yield of Laboratory Testing in Pediatric Ketogenic Diet Patients: Critical Assessment of Abnormal Results and Impact on Clinical Care.
Charuta Joshi, Chelsey Stillman, Stephanie Criteser, Alison Conley, Jennifer Oliver
Simultaneous quantification of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate, pipecolic acid and alpha-aminoadipic acid in pyridoxine-dependent epilepsy
Zhixian Yang, Jiao Xue, Pan Gong, Junjuan Wang, Minhang Wu, Wenshuang Yang, Shiju Jiang, Ye Wu, Yuwu Jiang, Yuehua Zhang, Tatiana Yuzyuk, Hong Li
COMPARISON OF CALCIUM LEVELS IN CHILDREN WITH FEBRILE SEIZURES AND CHILDREN WITH FEVER AND NO SEIZURES
Rekha Mittal, Shailabh Gupta, Naresh Bhatia
Some Neuropsychological factors as associated to cognitive functions of Mesial Temporal lobe epilepsy (MTLE) children.
Gopukumar Kumarpillai, Murthy G, Umashankar R, shobha Nandavar, Girish Gadre
Nitrazepam as first line treatment for Infantile Spasm-20 years’ experience from Tertiary Paediatric Neurosciences Centre
Jay Shetty, Paul Eunson, Celia Brand, kenneth McWilliam, Krishnaraya Kamath Tallur, Richard Chin, Ailsa McLellan
Low ratio ketogenic diet (KD) can achieve good seizure control in children with epilepsy
Rajesh RamachandranNair, Zeling Chen
Outcome Following Febrile Seizures: A Scottish Population Cohort
Libby CHATTERTON DICKSON, Ailsa McLellan, Paul Leonard, Clodagh Mitchell, Jay Shetty
PHOTOSENSITIVITY AND CLINICAL CHARACTERISTICS FROM A SCOTTISH POPULATION COHORT
Gareth Neo, Lauren Marie Smith, Leanne Brennan, Jay Shetty, Krishnaraya Kamath Tallur
Experience with Isoflurane in Paediatric Super Refractory Status Epilepticus
Ashwini Mohan, Lokesh Lingappa, Ramesh Konanki, Nikit Shah, Smilu Mohanlal, Farhan Shaikh, anupama Y, shashwat Mohanty
Effects rehabilitation with interactive metronome training on speech disorders and epilepsy patients.
Tatiana Tomenko
Epilepsia Partialis Continua (EPC) in children: Clinical presentation and underlying aetiologies
SNEHAL SURANA, Jane Hassell, Stewart Boyd, Helen Cross, Yael Hacohen
An Exploration of Prescribing Practice and Parental Use of Emergency Rescue Medication to Prevent Status Epilepticus in Children
Celia Brand, Ailsa McLellan
Protective effects of the ROCK inhibitor fasudil against cognitive dysfunction following status epilepticus in immature male rats
Song xiaojie
Our experience with use of new 2017 ILAE classification in children with epilepsy
Abhinav Sahu, Neeta Naik, AMI SHAH, Abhinav Tiwari
A Study of Reasons for Poor Response/ Poor Control of Epilepsy in Children on Polytherapy
nilima narkhede
MAGNITUDE OF CO-MORBIDITIES IN PEDIATRIC EPILEPSY: NEED FOR NEUROPSYCHOLOGICAL REHABILITATION
Somini Haresh Mehta, Urvashi Shah
Epilepsy burden in NHBI (Neonatal Hypoglycemic Brain Injury)
RITESH C SHAH
Retrospective cohort of Dravet syndrome due to SCN gene mutation from Southern India
Hemadriben Muljibhai Vegda, Vykuntaraju Gowda, Raghavendraswami Amoghimath, Asha benakappa
Evolution of electroencephalogram findings in pontocerebellar hypoplasia type 2A
Rony Cohen, Yoram Nevo, Sara Kivity, Ayelet Halevy, Sharon Aharoni, Rachel Straussberg
Infantile tremor syndrome followed by West Syndrome: A case series
Jasmine Singh
Tolerance to cannabidiol in children and adults with treatment-resistant epilepsy
Shimrit Uliel-Sibony, Moran Hausman-Kedem, Uri Kramer
EPILEPTIC ENCEPHALOPATHY DUE TO GABRG2 MUTATION
Angeles Schteinschnaider, Isaura Gonzalez, Eliana Julian, Julia Boccoli
Efficacy of zinc supplementation in preventing recurrence of febrile seizure in Bangalore
Ramya Ramesh, Rachel Ranitha Peterson, Carolin Elizabeth George
Two novel PCDH19 missense mutations in a mosaic male and a female epilepsy patients
Qian Peng, Haiming Yuan
systematic review of Perampanel in children and adolescent
ALPANA SANTOSH KONDEKAR, Rochana Redkar
Verbal Semantics and Social cognition in adolescents with drug resistant refractory epilepsy
Sujit Abajirao Jagtap, SONAL CHITNIS, KINJAL JAIN, ANKIT ARORA, MEDHA ADHYRU, SANDEEP PATIL, NILESH KURWALE
A hot and jerky child
Sonal Bhatia
Comparison of 1981, 1989 and 2017 International League Against Epilepsy classification (ILAE)
David Asish Manchala, Neelu Desai, Payal Shah, Vrajesh Udani
Assessment of quality of life in Omani children with epilepsy attending Sulatan Qaboos University Hospital
Amna Mohamed Al Futaisi
Mammalian Target of Rapamycin (mTOR) Inhibitors as an Effective Therapy for Refractory Epilepsy associated with Tuberous Sclerosis Complex: A Systematic Review
ALPANA SANTOSH KONDEKAR, mayank Detroja
Dandy Walker malformation with epileptic spasms
Gürkan Gürbüz
Effectiveness and Safety of high-dose, Oral Pyridoxine as an adjunct to high-dose Adrenocorticotrophic hormone versus high-dose Adrenocorticotrophic hormone alone for the treatment of West Syndrome: An Open-Label, Randomized Control Trial
Arundhati Banerjee, Jitendra Kumar Sahu, Naveen Sankhyan, Smita Pattanaik, Renu Suthar, Arushi Gahlot Saini, Lokesh Saini, Prahbhjot Malhi, Pratibha Singhi
SPECTRUM OF TUBEROUS SCLEROSIS COMPLEX - CLINICAL PROFILE IN A COHORT OF 48 CHILDREN
Leema Pauline Cornelius
Valproic Acid: A potion with caution
ALPANA SANTOSH KONDEKAR, swarupa bansode
Etiology of Epilepsy In a developing Country – A study from a tertiary Pediatric Hospital
David Asish Manchala, Neelu Desai, Rahul Badheka, Vrajesh Udani
Bones and brains: a prospective case-control study of seasonal vitamin D in childhood epilepsy
Celia Brand, Ailsa McLellan, Sonia Joseph, Richard Chin
X-LINKED EPILEPTIC INFANTILE ENCEPHALOPATHY OF UNUSUAL INHERITANCE
Angeles Schteinschnaider, Solange Gril, Mercedes Villanueva, Agatha Fernandez, Horacio Martinetto, Ezequiel Surace
SYNCOPE IN CHILDREN-CLINICO-ETIOLOGICAL CORRELATION
MADHURA FADNIS
Severe neonatal epileptic encephalopathy secondary to a mutation of the ATP1A3 gene
Thouraya Ben Younes, Hanene Benrhouma, Hedia Klaa, Aida Rouissi, Myriam Chaabouni, Ichraf Kraoua, Ilhem Ben Youssef-Turki
Telephone based follow-up of children with Epilepsy aged 4 months to 18yrs: comparison of accuracy between a Specialty Nurse and a DM Pediatric Neurology Fellow to identify Critical Clinical Events requiring Face-to -Face evaluation
Sheffali Gulati, Prashant Jauhari, Shruti N M, Prateek Kumar Panda, Mable Jossy, Biswaroop Chakrabarty, R M Pandey
Epilepsy in Children- Psychosocial and Emotional Impact on Their Siblings and Their Coping Skills
EKTA AGARWAL, Dr. Kavita Srivastav, Dr. Surekha Rajadhyaksha, Dr. Manjiri Datar
LANGUAGE EVALUATION IN GENETIC EPILEPSY FEBRILE SEIZURES + SYNDROME – A PROSPECTIVE CONTROLLED OBSERVATIONAL STUDY
Toral Bhatt, Vrajesh Udani, Megha Shah, Neelu Desai, somini mehta
EFFECT OF LONG-TERM ANTIEPILEPTIC DRUGS ON BONE MINERAL METABOLISM AND THYROID PROFILE IN INDIAN CHILDREN:A CASE CONTROL STUDY
Devaraja Sethi, Kavita Srivastava, Surekha Rajadhyaksha, Anuradha Khadilkar
Epidemiological Survey (three staged) of Pediatric Epilepsy in a rural suburb of Pune District
EKTA AGARWAL, Dr. Surekha Rajadhyaksha, Dr. Kavita Srivastav
Clinical and therapeutic profile of childhood epilepsy in an Onchocerciasis-endemic rural Area
Dominique ENYAMA
Asymptomatic malaria parasitaemia and seizure control in children with nodding syndrome; a cross sectional study
Rodney Ogwang, Ronald Anguzu, Pamela Akun, Albert Ningwa, Edward Kayongo, Kevin Marsh, Charles Newton, Richard Idro
Prevalence of Seizures among children admitted with BRUE (Brief resolved unexplained event)
Lamyaa Jad
EFFECT OF ACTH COMBINATION THERAPY VERSUS ACTH ALONE IN WEST SYNDROME: A RETROSPECTIVE STUDY
Devaraja Sethi, Kavita Srivastava, Surekha Rajadhyaksha
Clinical Profile of Epilepsy in Neonatal Hypoglycemic Brain Injury.
Madhavi Shelke, Shirish Bhartiya, Varsha Vaidya, Sandeep Saraf
Kabuki Syndrome and Effectiveness of Perampanel
Manoj Vasireddy
Comparison between Melatonin and Diazepam for Prevention of Recurrent Simple Febrile Seizures: Randomized clinical trial
amira darwish
Clinical spectrum and therapeutic outcomes of electrical status epilepticus during sleep in children
Bing-Wei PENG, Hai-Xia Zhu, Xiu-Ying WANG, Xiao-Jing LI, Hui-Ci LIANG, Feng-Qiong ZHANG, SHu-Yao Ning, Yan-Ying Zhong, Wen-Xiong Chen
Febrile Infection Related Epilepsy Syndrome (FIRES) – A rare cause of super refractory status epilepticus
Aanchal Pradeep Khemani, Sanjay Bafna, Sagar Lad, Nandan Yardi
Clinicoetiological profile and outcome of convulsive status epilepticus in children
Rajwanti Kishore Vaswani, Sayoni RoyChowdhury
“Me and My Epilepsy”: A qualitative study of Children’s Experiences and a novel child-centered animation about epilepsy
Rebecca Black, Jeni Harden, Martyn Pickersgill, Jay Shetty, Ailsa McLellan, Celia Brand, Michelle Small, Richard Chin
Neonatal-onset epilepsy: Clinico-etiological spectrum and short-term outcome
Prasanthi Aripirala, Ramesh Konanki, Lokesh Lingappa
Utility of short term video EEG recording in diagnosis of paroxysmal events in children
abhinav ashok tiwari, neeta naik, ami shah, abhinav sahu
Polypharmacy in childhood epilepsy syndrome management: overuse or underuse of a diagnostic tool?
selina husna BANU, SELINA HUSNA BANU, Naila Zaman KHAN
Continuous Spikes and Waves during Slow-Wave Sleep (CSWS) in Children: The Epilepsy Syndrome that Can’t Stop, Won’t Stop
Arushi Gahlot Saini, Naveen Sankhyan, Prahbhjot Malhi, Niranjan Khandelwal, Pratibha Singhi
Infantile spasms following Acquired brain injury - A tertiary Neuro-Rehabilitation centre experience
Archana Murugan
Oral Ketamine is an Effective and Safe Treatment for Non-Convulsive Status Epilepticus
Archana Murugan
A Prospective Study of Non-Epileptic Events in Children with Intractable Epilepsy
Shermila Pia, Andrew Mallick, Elliot Warren, Nick Kane
Transition to adult medical care for adolescents with epilepsy-identifying care gaps in current models: Perspectives from a UK neurology tertiary centre
Thomas Robb
EPEMA (encephalopathy,petechiae and ethylmalonic aciduria) – a case series.
KAPIL JETHA, Vykuntaraju K Gowda, Varun M Srinivas, Meenakshi Bhat, Maya Bhat, Christopher Rita, Asha Benkappa
Cohort of Clinical profile and Outcome of Pyridoxine dependent epilepsy
KAPIL JETHA, Vykuntaraju K Gowda

Headache

Barriers to Care among Indian Children with Recurrent Headache
Charu Jain, Devendra Mishra, Monica Juneja, V Pavithra, Deepti Chawla
The Perception and Performance of Headache Management among School Health Teachers
Young-Il Rho, Shin-Young Park, Mi-Sun Jang
Examination of children with migraine; Three years experience
Deniz Karakaya, Deniz Yüksel, Hülya Kayılıoglu, Ayşe Aksoy, Ulkuhan Oztoprak, Çigdem Genç Sel, Erhan Aksoy, Ozge Dedeoglu
COMPARISON OF THE LIFESTYLE PATTERNS OF CHILDREN WITH RECURRENT PRIMARY HEADACHE WITH THOSE OF CHILDREN WITH NO HEADACHE IN FIVE TO EIGHTEEN YEARS AGE
Rekha Mittal, Lakshmi Narain Taneja, Sumit Kumar Dwivedi
Factors Predicting Migraine in Pediatrics Patients with Asthma: A National Perspective
Riddhiben patel, vandana vedanarayanan, jagdish desai
P300 scores and neurobehavioural profile of children with primary headache
Jyotindra Narayan Goswami, Saroj Kumar Patnaik
Relapsing factors for pediatric migraine
KON-HEE LEE
Arterial Spin Labelling Perfusion Weighted Imaging (ASL-PWI) in Pediatric Hemiplegic Migraine: Clinico-radiological Correlation
Badal G Jain, Rahul Nikam, Tara Pezzuto, Rachit Patil, Vinay Kandula
Assessment of the association between pediatric Idiopathic Intracranial Hypertension and olfactory function
Maya Muhlbauer Avni, Naama Yosha-Orpaz, Osnat Konen, Nitza Goldenberg-Cohen, Rachel Straussberg
IDIOPATHIC INTRACRANIAL HYPERTENSION IN CHILDREN- IS IT REALLY IDIOPATHIC?
Sumeet Rajendra Dhawan, Lokesh Saini, Raviteja Indla, Indar Sharawat, Akshay Saxena, Sameer Vyas, R K Sharma, Arushi Gahlot Saini, Renu Suthar, Jitendra Sahu, Naveen Sankhyan

Metabolic Disorders

Pyridoxine dependent epilepsy: beyond ALDH7A1 gene mutation
ROSHAN KOUL
A RARE CAUSE OF STRIDOR & RECURRENT CENTRAL APNEA: MAPLE SYRUP URINE DISEASE
RAVI SHARMA, SAKSHI SHARMA, VIVEK JAIN, LALIT BHARADIA
DIAGNOSIS OF GM2 GANGLIOSIDOSIS WITH A NEW MUTATION
Rashmi Adiga, Neha Rajkumar Jain, Sudhindra Kulkarni, Kruti Varshney
Leigh-like syndrome due to homoplasmic m.8993T>G variant with hypocitrullinemia and unusual biochemical features suggestive of multiple carboxylase deficiency (MCD)
Maina Padmanabha Kava, Barry Lewis, Lawrence Greed, Shanti Balasubramaniam
Large-single scale mitochondrial DNA deletions in different tissues of patients with Kearns-Sayre syndrome
yuqing shi, fang fang, zhimei liu
Long-term follow-up and Clinical findings of BH4 deficiency patients in Korea
Eun Sook Suh
Three Cases Of Creatine Deficiency Syndromes Caused By GAMT Gene Mutation
Lei Yang, Fang Fang
Expanding the phenotype of TRNT1 mutations to include Leigh syndrome.
Carolina Gorodetsky, Chantal F. Morel, Ingrid Tein
Fatal neonatal lactic acidosis secondary to a novel defect in COX16 causing complex IV deficiency
Maina Padmanabha Kava, Shanti Balasubramaniam, Barry Lewis, Richard Rodenburg
TRPM6 gene mutation resulted in primary hypomagnesemia with secondary hypocalcemia(HSH) in 3 cases
xiaohui wang, shen zhang, weihua zhang, jiuwei li, changhong ding, fang fang
NEWLY IDENTIFIED TOTALLY TREATABLE METABOLIC ENCEPHALOPHY: Biotin-Thiamine Responsive Basal Ganglia Disease
TARISHI NEMANI, PUJA MEHTA, Purva Keni karnavat, ANAITA UDWADIA HEGDE
Phosphoserine aminotransferase deficiency: MRI Findings.
Alcy Torres, Zakir Iqbalbhai Shaikh, Bindu Setty
Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Presentation
Ceren Günbey, İnci Türkan Yılmaz, İbrahim Taş, Meral Topçu
Profile of Peroxisomal Disorders in infancy and childhood
Lobna Abdelgawad Mansour, Ekram Mohamed Fateen, Mohamed Ahmed Rashed, Hoda Ahmed Marzouk, Dina Mohamed Hesham, Lamia Tarek Tawfik
Argininemia in 3 siblings- different phenotypes in the same family
Aman Elwadhi, Suvasini Sharma, Bijoy Patra
Gene therapy improves global development in AADC deficiency
Takanori Yamagata, Karin Kojima, Akihiko Miyauchi, Takeshi Nakajima, Naoyuki Taga, Sachie Nakamura, Mitsuhiro Kato, Hitoshi Osaka, Shin-ichi Muramatsu
Hypocalcemia as a cause of breath holding spells in children below 6 months
Simran Jain, Neha Ahuja, Gouri Rao Passi
An unusual presentation of Menkes disease masquerading as a leukodystrophy with macrocephaly
Aswini Annadurai, Anshula Tayal, Aman Elwadhi, Suvasini Sharma, Bijoy Patra
A rare cause of developmental delay
Sakshi Batra, Aman Elwadhi, Suvasini Sharma, Bijoy Patra
A case report on siblings with motor regression and dystonia
Abhishek Jain, Aman Elwadhi, Suvasini Sharma, Bijoy Patra
Neurometabolic profile of macrocephaly in infancy and childhood, Biochemical and molecular study
Lobna Abdelgawad Mansour, Ekram Mohamed Fateen, Mohamed Ahmed Rashed, Ezzat Mohamed Elsobky, Solaf Mohamed Mohamed, Lamia Tarek Tawfik
Case of two brothers with Cerebrotendinous Xanthomatosis presenting with Progressive Myoclonic Epilepsy
Karan Desai, Sangeeta Ravat, Viraj Sanghi, Piyush Kumar, Priyanka Walzade, Neeraj Jain
A case series of four patients of Menkes disease -clinico radiological presentation with usual and unusual features.
umesh dinkar kalane, Umesh Dinkar Kalane, Surekha Rajadhyaksha
Assessment of Vitamin B-12 deficiency and Risk Factors in Healthy Infants: A Cross-sectional Study
Kuchana Suresh Kumar, Savita Attri, Arushi Gahlot Saini, Bhavneet Bharti, Naveen Sankhyan, Prateek Bhatia, Ajay Patial
Gelastic cataplexy leading to the diagnosis of Niemann-Pick disease type C
Ezgi Oktener Anuk
A Missed Diagnosis: Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase Deficiency with Unilateral Basal Ganglia involvement in an Adolescent Boy
ALPANA SANTOSH KONDEKAR, mayank Detroja
CONGENTIAL METHEMOGLOBINEMIA TYPE 2: A RARE CAUSE OF NEURODEVLOPMENTAL DELAY
vishal bhansali, sanjay bafna
BIOTINIDASE DEFICIENCY: A TREATABLE CAUSE OF REFRACTORY EPILEPSY IN INFANCY
SHIKHA JAIN
Clinical and genetic analysis in three Chinese patients with congenital disorder of glycosylation
Changhong Ren, Fang Fang, Changhong Ding
GLUTARIC ACIDURIA TYPE 1: AN USUAL IMAGING FEATURE
SHRUTI HARSHAL AGRAWAL, SANGEETA RAVAT, VIRAJ SANGHI
Spectrum of Inherited White Matter Disorders in Children and their Outcomes
Vijay Gonda, Arushi Gahlot Saini, Naveen Sankhyan, Jitendra Sahu, sameer vyas, Savita Attri, Inusha panigrahi
Kangaroo gait as a presentation of Hyper-manganesemia
Akash Harakchand Chheda, Vrajesh Udani, Hina Faldu
All that glitters is not gold: A lesson to learn.
abhijeet vilas botre
Lysine- restricted diet in a child with pyridoxine -dependant epilepsy prevents long term developmental delay
Leah Queit, Maina Padmanabha Kava, Barry Lewis, Lawrence Greed, Peter Williams Rowe, Shanti Balasubramaniam
Treatable Leigh syndrome involving mitochondrial cofactor metabolism
Zhimei Liu, Fang Fang
Infantile-onset mitochondrial disorder associated with COQ4 missense mutations
Leechin Wong, WangTso Lee
Does Thiamine help in Wilsons disease management?
MAHESH ARUN SAMBHARE
Pediatric neurotransmitter disorders: single center experience in India
Rahul Badheka, Vrajesh Udani, Neha Inamdar
Clinico-biochemical profile and outcome of children with Inborn Errors of Metabolism (IEM)
Bidisha Banerjee, Supriya Shinde, Rita Christopher
A novel mutaion in HTRA2 causes mitochondrial disorder associated with early infantile onset epileptic encephalopthy,movement disorder and 3 methyl glutaconic aciduria
Harshkumar Arvindbhai Patel
A proposed staging system for CLN3 disease (Juvenile Batten Disease)
Jonathan W Mink, Justin Williams, Erika Augustine
MTHFR Deficiency Heavy Form going with Demyelinating Leukodystrophy and Psychomotor Retardation
MESUT GUNGOR, BULENT KARA
The Clinical feature of Urea cycle disorders in China
Li Jiang
Analysis of 154 cases with mitochondrial DNA variations in Chinese children with mitochondrial disorders
yuqing shi
The Unified Batten Disease Rating Scale (UBDRS): Validation and Reliability in an Independent Sample
Jonathan W Mink, Miriam Nickel, Eva Wibbeler, Christoff Schwering, Angela Schulz
Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET) imaging and motor and sensory neurophysiology in children with Glutaric Aciduria(GA1) dystonia awaiting Deep Brain Stimulation Surgery (DBS)
Stavros Tsagkaris, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Verity McClelland, Alexander Hammers, Jean-Pierre Lin
Clinical and genetic analysis of progressive cavitating leukoencephalopathy in China
Ren Changhong, Fang Fang, Zhimei Liu
NEUROREGRESSION IN CHILDREN – CLINICAL SPECTRUM AND INVESTIGATION PROFILE IN CHILDREN ATTENDING NEUROLOGY OUTPATIENT
Ayesha Mariam, vishwanathan venkataraman
Clinical profile of Indian children with type 1 citrullinemia at a Tertiary care referral centre in Southern India – A Descriptive study
Balamurugan N, Vykuntaraju K Gowda, Rita Christopher, Asha Benakappa
Clinical profile of children with type 1 Glutaric aciduria at a Tertiary care referral centre in Southern India – A Descriptive study
Balamurugan N, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Asha Benakappa
Spectrum of riboflavinopathies from southern India - A desrciptive study
Arundhati Patil
Severe preeclampsia could be the sign of long-chain fatty acid oxidative enzyme deficiency
Selda Bülbül, Uğur Can Kara
Lysosomal Storage Diseases: Experiences of Kırıkkale University
Selda Bülbül, Cansu Çelik, Elif Gökçe Ünal
Importance of Influenza vaccination in Urea Cycle Disorders
Selda Bülbül, Cansu Çelik, Elif Gökçe Ünal

Movement Disorders

A novel frameshift mutation in SLC2A1 (GLUT1) associated with a mild form of carbohydrate-responsive movement disorder
Yasser Awaad
High dose of levodopa and Segawa disease
Madina Taghiyeva
GENETIC SPECTRUM OF PEDIATRIC MOVEMENT DISORDERS
Kritika Tiwari, TARISHI NEMANI, Purva Keni karnavat, ANAITA UDWADIA HEGDE
Utility of Deep Brain Stimulation in Pantothenate Kinase Associated Neurodegeneration(PKAN)
Puja Mehta, Purva Keni, Anaita Hegde
Management of Status Dystonicus in Children: Reporting of 3 cases with videos.
Kanij Fatema
A Rare Case Of Early Onset Hereditary spastic paraplegia caused by AFG3L2 and SPG7 mutations
Piyush Kumar Anshu, Dr Viraj Sanghi
Paroxysmal exercise induced dyskinesia in siblings — A rare cause
Senthilkumar Vajramanickam
An Imaging Clue for Treatable Early Childhood-Onset Dystonia - Manganism
Hansashree Padmanabha, Savita Krishnamurthy, Sharath Kumar G G, Indumathi Chikkanayakana
Anti-NMDAR Encephalitis in Children ; a Malaysian Experience
Balakrishnan Priyalatha, Tajudin Tajul Arifin, Vigneswari G
Rett syndrome in Taiwan: genotype and phenotype characteristics
Leechin Wong, WangTso Lee
Atypical Presentations of Anti-NMDAR encephalitis – A Report of 3 Interesting Cases
Balakrishnan Priyalatha, Tajudin Tajul Arifin
Two Different Phenotypes of Tyrosine Hydroxylase Deficiency Syndrome
Punita Chandra Segaran, Tajudin Tajul Ariffin
A tripping kid- Unusual presentation of GLUT 1 Deficiency Syndrome
Jigyasha Sinha, Anirban Ghosal, Hrishikesh Kumar
Transcranial magnetic stimulation in the treatment of Tourette's syndrome in children: A pilot study
Cynthia K Kahl, Adam Kirton, Tamara Pringsheim, Paul Croarkin, Rose Swansburg, Ephrem Zewdie, Frank P MacMaster
Spectrum of movement disorders in children – types, etiology, severity and response to therapy
Chandrashekhar Pandey, Hardeep Singh Malhotra, Chandrakanta Kumar, Rashmi Kumar
Unusual Presentation of 4H Syndrome as Post Varicella Ataxia
Ridhimaa Jain, Aman Elwadhi, Suvasini Sharma, Nicole Wolf, Resie M van Spaendonk, Bijoy Patra
PROGRESSIVE AND SEVERE MOVEMENT DISORDER IN A PATIENT CARRYING A GNAO1 MUTATION RESPONSIVE TO DEEP BRAIN STIMULATION
Angeles Schteinschnaider, Mercedes Villanueva, Milagros Beltramo, Agata Fernandez, Ezequiel Surace, Horacio Martinetto
THE EFFECT OF RISPERIDONE IN IMPROVING MOTOR AND FUNCTIONAL DISABILITY IN CHILDREN WITH CHOREO-ATHETOID CEREBRAL PALSY: A ONE YEAR PROSPECTIVE STUDY AT A TERTIARY CARE CENTRE
Nishant Mittal
“Distinctive upper limb dystonia as a correlate to the ‘Eye of tiger’ MRI sign.”
Akash Harakchand Chheda, Satish Khadilkar, Vrajesh Udani
CHILDHOOD ONSET CHRONIC ATAXIA: A CLINICAL, ETIOPATHOLOGICAL, RADIOLOGIC AND GENETIC AUDIT.
Pallavi Shriram Todase, shilpa kulkarni, sonam kothari, anaita hegde, krishankumar shah
Can early onset ataxia phenotypically be distinguished from developmental coordination disorders?
Tinka Lawerman, Rick Brandsma, Natasha M Maurits, Octavio E Martinez-Manzanera, Roelineke J Lunsing, Oebele F Brouwer, Hubertus PH Kremer, Deborah A Sival
A novel mutation in KMT2B gene causing childhood-onset generalized dystonia
Tanmayee Subhash Thombare
A Diagnostic Algorithm for Early Onset Ataxia
Rick Brandsma, Corien Verschuuren, Oebo Brouwer, Hubertus Kremer, Tom de Koning, Marina de koning-Tijssen, Deborah Sival
Clinical clues in etiological diagnosis of childhood ataxia
EKTA AGARWAL
Profile of Neuronal Brain Iron Accumulation in Pediatric population: experience from a tertiary care centre in North India
Ankita Pal, Prateek Kumar Panda, Biswaroop Chakrabarty, Prashant Jauhari, Vishal Sondhi, Rajni Farmania, Atin Kumar, Manisha Jana, Sheffali Gulati
Early Onset Ataxia and Comorbid Dystonia: Are There Shared Biological Pathways?
Deborah Anita Sival, Marina Tijssen, Dineke Verbeek
PONTOCERREBELAR HYPOPLASIA SUBTYPE 1B (EXOSC3 MUTATION): CASE REPORT
Fernanda Noemi Moreira, Nicolas Espinosa
Tics in a child with Hashimoto encephalopathy
Padma Balaji, Vasanthi Thiruvengadam, Ashish Badaya
Writer’s cramp in children- A case series
dipa saha
Multimodal immunotherapy in a patient with opsoclonus-myoclonus-ataxia syndrome - case report
Tomasz Mieszczanek
The Tonic Labyrinthine Response (TLR) also known as “Scissoring” is a hallmark of Dystonia
Federica Graziola
Spinocerebellar ataxia 35
Manimala S
Status dystonicus in Children: A Nightmare for both the Physician and the Patient
Arushi Gahlot Saini, Kanika Goyal, Sumeet Dhawan, Lokesh Saini, Renu Suthar, Jitendra Sahu, Naveen Sakhyan, Jayashree Muralidharan, Pratibha Singhi
Motor and sensory neurophysiology in childhood dystonias correlate with distinct resting glucose brain metabolism patterns using [18F]FDG PET-CT imaging and may help characterise the prognosis of deep brain stimulation (DBS) neuromodulation
Stavros Tsagkaris, Verity McClelland, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Teresa Szyszko, Alexander Hammers, Jean-Pierre Lin
Tourette syndrome -a developmental dopamine disorder
Yoshiko Nomura
Segawa Disease- 47 years since the first description -Revisit of its clinical features and pathophysiology
Yoshiko Nomura

Muscle and Nerve

Incidence of infantile spinal muscular atrophy in Shikoku Island of Japan
Kentaro Okamoto, Mitsumasa Fukuda, Isao Saito, Risako Urate, Satoshi Maniwa, Daisuke Usui, Takahiro Motoki, Toshihiro Jogamoto, Kaori Aibara, Takatoshi Hosokawa, Yukihiko Konishi, Reiko Arakawa, Kenji Mori, Eiichi Ishii, Kayoko Saito, Hisahide Nishio
Rigid spine syndrome: A report of 15 children
ROSHAN KOUL
Childhood Onset Limb Girdle Muscular Dystrophies in Aegean Part of Turkey
Uluç Yiş, Gülden Diniz, Filiz Hazan, hülya sevcan daimagüler, bahar toklu baysal, figen baydan, gülçin akıncı, aycan ünalp, gül aktan, erhan bayram, semra hız, cem paketçi, derya okur, erdener özer, ayça ersen danyeli, gökhan uyanık, sebahattin çırak
Differentiation between inflammatory myopathies and genetic muscle disease
xingzhi chang
Diagnostic Potential of Next Generation Sequencing in Suspected Genetic Neuromuscular Disorders
Dr Vishal Kanubhai Patel, Purva Keni Karnavat, Anaita Udwadia Hegde
Spinal Muscular Atrophy – Lower Extremity Dominant Type 2 (SMALED2)
Erdem Simsek, Sanem Yilmaz, Hepsen Mine SERIN, Seda Kanmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben
UK initiative to speed up diagnosis of Duchenne muscular dystrophy worldwide
Henriette van Ruiten, Mayhew Anna, Helen Aspey, Robert Muni Lofra, Volker Straub, Michela Guglieri
Pain prevalence and characteristics in spinal muscular atrophy type II
Yuu Uchio, Mikiko Hasegawa, Kouta Kajima, Hayato Suzuki, Kaho Nakamura, Midori Saito, Tetsuo Ikai, Futoshi Wada, Kayoko Saito, Reiko Arakawa, Osamu Nitta
Atypical childhood-onset neuroaxonal dystrophy in an Indian girl - case report
Himani Bhasin, Sakshi Jain, Marta Romani, Enza Maria Valente, Suvasini Sharma
STUDY OF CYTOKINE (IL-2, IL-6, TNF-α, Interferon-ϒ, IL-17) LEVELS IN ACUTE GUILLAIN-BARRE SYNDROME
JAYANTH KRISHNA MADUGULA
Neuromusclar transmission defect in FKRP congenital muscular dystrophy
Kenneth McWilliam, Linda McLellan, Lisa Robertson
Bone Health Monitoring In Boys With Duchenne Muscular Dystrophy: A Survey Of Clinical Practice In The United Kingdom NorthStar Clinical Network
Shuko Joseph, Nadia Capaldi, Marina DiMarco, Iain A Horrocks, Volker Straub, S Faisal Ahmed, Michela Guglieri, Sze Choong Wong, North Star Clinical Network
The Efficacy of Acyclovir in Childhood Bell’s Palsy
Gürkan Gürbüz
Received care by brazilian patients with Duchenne Muscular Dystrophy
Clarisse Pereira Dias Drumond Fortes
Combination of Topiramate and Lacosamide is Effective for Paramyotonia Congenita with neurological symptoms
Yoshie Kurokawa, Akihiko Miyauchi, Akihiko Miyauchi, Hirokazu Yamagishi, Hirokazu Yamagishi, Eriko Jimbo, Eriko Jimbo, Kazuhiro Muramatsu, Kazuhiro Muramatsu, Hitoshi Osaka, Hitoshi Osaka, Takanori Yamagata, Takanori Yamagata
Impact of genetic results on treatment of CONGENITAL MYASTHENIC SYNDROME (CMS)
RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, BINDU MADHAVI PARICHURI, SMILU MOHANLAL
A Toddler with Myasthenia Gravis Ocular
alifiani hikmah putranti
Vamorolone, the first dissociative steroidal anti-inflammatory, improves muscle function and shows limited side effects in Duchenne muscular dystrophy (DMD): results of Phase IIa studies in 48 DMD boys.
Michela Guglieri, Kanneboyina Nagaruja, Paula Clemens, Jesse Damsker, John McCall, Edward Smith, Diana Castro, Jean Mah, Craig McDonald, Nancy Kuntz, Richard Finkel, Mar Tulinius, Yoram Nevo, Monique Ryan, Richard Webster, Andrea Smith, Lauren Morgenroth, Eric Hoffman, Laurel Mengle-Gaw, Laurie Conklin
CONGENITAL MYASTHENIA SYNDROME: CLINICAL PROFILE, TREATMENT RESPONSE, ELECTRODIAGNOSTIC STUDIES AND GENETIC AUDIT .
Pallavi Shriram Todase
Guillain-Barre Syndrome: Uncommon association to common pediatric diseases
Marwa Abd Elmaksoud, Yasmine El Chazli, Shaymaa Elsayed
Design of a phase 3 trial to evaluate the long-term efficacy and safety of ataluren in patients with nonsense mutation Duchenne muscular dystrophy
Francesco Bibbiani, Panayiota Trifillis, Edward O'Mara, Joseph McIntosh
Long-term Pulmonary Function Outcomes in Non-Ambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy Treated with Ataluren: 240-Week Data from an Open-label Extension Study
Craig M McDonald, Craig Campbell, Eugenio Mercuri, Francesco Muntoni, Kathryn Selby, Francesco Bibbiani, Panayiota Trifillis, Joseph McIntosh, Marcio Souza, Stuart W Peltz, Mar Tulinius
CARDIOPULMONARY ASSESSMENT IN CHILDREN WITH DUCHENNE MUSCULAR DYSTROPHY
Priyanka Madhukar Meshram
Late onset LAMA-2 Deficiency Congenital Muscular Dystrophy
Amarinder Singh Oberoi, Krishnakumar N Shah
Ragged red fibers in myopathy with white matter changes - mitochondrial disorder or a red herring?
Bijoy Patra, Helman Guy, Suvasini Sharma, Puneet Jain, Ravinder Kumar Saran, MS Van Der Knapp
Meta-analyses of ataluren in patients with nonsense mutation Duchenne muscular dystrophy
Craig Campbell, Francesco Muntoni, Eugenio Mercuri, Gary L Elfring, Panayiota Trifillis, Francesco Bibbiani, Stuart W Peltz, Craig M McDonald
Preservation of Function over time as Measured by North Star Ambulatory Assessment in Ambulatory Boys with Nonsense Mutation Muscular Dystrophy Treated with Ataluren
Craig M McDonald, LJ Wei, Gary L Elfring, Panayiota Trifillis, Francesco Bibbiani, Marcio Souza, Joseph McIntosh, Stuart W Peltz, Francesco Muntoni
Clinical profile and benefit from riboflavin in BVVL due to RFVT2 deficiency
Manoj Peter Menezes, Kayla Cornett, Gabrielle Donlevy, Joshua Burns
Multiplex ligation-dependent probe amplification based SMN1 deletion analysis in 150-Indian patients with spinal muscular atrophy
Hansashree Padmanabha, Veeramani Preethish-Kumar, KIRAN POLAVARAPU, Saraswati Nashi, Seena Vengalil, Deepha Sekar, Nalini Atchyaram, Priya Thomas, KRISHNA GK
Spinal Muscular Atrophy, a single centre experience
Ann Agnes Mathew
EARLY CLINIC-ELCTROPHYSIOLOGICAL PREDICTORS OF POOR FUNCTIONAL OUTCOMEIN GBS
EKTA AGARWAL
Duchenne Muscular Dystrophy a South Indian Perspective
Ann Agnes Mathew
Explore evaluation methods of treatment efficacy on spinal muscular atrophy
kotaro yuge, Masao Suda, Ryuta Ishii, Takashi Ohya, Shinichiro Nagamitsu, Motomu Yoshida, Yushiro Yamashita
Double-blinded Randomized Placebo Controlled trial of Valproate and levocarnitine in Children with Spinal Muscular Atrophy (aged 2-15years)
Sheffali Gulati, Biswaroop Chakrabarty, Jaya Shankar Kaushik, Ranjith Kumar Manokaran, Priyanka Madaan, Prabhjot Kaur, Madhulika Kabra, Sumita Bisoi, Sanjay Wadhwa, R M Pandey, Y K Gupta
Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy
Ranjith Kumar Manokaran, Biswaroop Chakrabarty, Prashant Jauhari, Rakesh Kumar, Sandeep Aggarwala, Arun Gupta, Manisha Jana, R M Pandey, Sheffali Gulati
Case series - congenital myasthenia gravis genotype and phenotype co-relation
Rujuta Joshi
Hereditary Sensory and Autonomic Neuropathy Type VII- A Rare Presentation
Maroti Kadam, Swati Gupta, Mamta Muranjan, Rajwanti K Vaswani
Etiological Profile of Hereditary Muscular Weakness in Pediatric Outpatients in Northern India
Prateek Kumar Panda, Prashant Jauhari, Biswaroop Chakrabarty, M C Sharma, Vaishali Suri, Chitra Sarkar, Madhulika Kabra, Sheffali Gulati
Phenotype-Genotype correlation ofa cohort of children with genetically confirmed Congenital Myasthenic Syndrome
mukul malhotra, Karthik Muttusamy, Sangeetha Yoganathan, Maya Mary Thomas, Pavalan Paneer, sumita Danda
Pulmonary functions in children with dystrophinopathy aged 5-18 years on oral steroid therapy for at least six months
Ankit Meena, Biswaroop Chakrabarty, Kana Ram Jat, S K Kabra, Sheffali Gulati
Genetic evaluation of Congenital Myopathy (CM) and Congenital Muscular Dystrophy (CMD) in children : Slow Death of Muscle biopsies
RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, PRASHANTHI ARIPRALA, RAMPRASAD VL, THENRAL SG
Schwartz-Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation
Gürkan Gürbüz
Anti –HMG-Co A reductase antibodies associated with progressive necrotizing myositis and autophagosomes in a teenager
Eleanor Ng, Maina Padmanabha Kava, Peter Williams Rowe, Simon Williams, Phillipa Lamont, Rei Curd Junckerstorff
Clinical profile of three children with HSAN type 4 from South India
Beena Suresh, Beena Suresh, Sujatha Jagadeesh
Guillain-Barré syndrome in a pediatric tertiary center (last five years)
Mafalda Sampaio, Cristina Garrido, Ruben Rocha, Marcio Cardoso, Ana Paula Sousa, Teresa Temudo, Sónia Figueiroa, Ines Carrilho, Manuela Santos
McArdle disease: a diagnosis to suspect in the paediatric age
ruben Rocha, Cristina Garrido, Ana Cardoso, Manuela Santos
Clinical and genetic characteristics of congenital myasthenia syndrome with episodic apnea caused by CHAT gene mutation in China
Zhimei Liu, Fang Fang
Comparison of five different electrophysiological criteria for Childhood Guillian Barre Syndrome
ANANTHANARAYANAN KASINATHAN, Arushi Gahlot Saini, Renu Suthar, Lokesh Saini, Jitendra K Sahu, Pratibha Singhi, Sunit Singhi, Naveen Sankhyan
A case series of hereditary sensory autonomic neuropathy in children
Renu Suthar, Hansa Shree Padmanabha, Arushi Gahlot Saini, Jitendra K Sahu, Bhavneet Bharti, Naveen Sankhyan, Ingo Kurth, Pratibha Singhi
A Case of Congenital Myasthenia with False Positive Anti-acetylcholine Receptor antibody
Chee Geap Tay, Limin Li, Chin Seng Gan, Chee Ming Teh, Vigneswari Ganesan, Choong Yi Fong
Clinical and genetic characteristics of GDAP1 gene mutation in Charcot Marie Tooth disease
JUN LAN LU, JUN LAN LU
Somatosensory Evoked Potential: a normative study in children
DILIP THAKUR
A pediatric case of anti-MuSK-antibody-positive ocular myasthenia gravis
Jeesuk Yu
Paediatric Gullain Barre syndrome and its variants – observation of clinico-electrophysiological profile in a tertiary care hospital
Sufia Khatun Sumi
Factors influencing initial diagnosis of Guillain Barre syndrome : A retrospective analysis
Padma Balaji, Vasanthi Thiruvengadam
SHORT TERM NEUROLOGICAL OUTCOME OF A COHORT OF ACUTE ASYMMETRIC FLACCID MYELITIS
lokesh saini
Disorders of Neuromuscular transmission in children: experience of a tertiary centre from North India
Priyanka Madaan, Biswaroop Chakrabarty, Prashant Jauhari, Aparajita Gupta, Rajni Farmania, Vishal Sondhi, Rachna Dubey, Sheffali Gulati
Collagen VI related myopathies: clinical variability of triple-helical domain mutations of COL6A mutations
Sophelia HS Chan, Ka Yee Anna Kwong, Ho Ming Luk, Fai Man Ivan Lo, Tsui Hang Sharon Fung, Ho Yin Mandy Tsang, Ho Yin Brian Chung, On-Kei Angel Chan
Clinicopathological profile and treatment outcome of Inflammatory myopathies in children: a retrospective cohort study
Prateek Kumar Panda, Vyshakh Anand, Prabhjoth Kaur, Prashant Jauhari, Biswaroop Chakrabarty, Atin Kumar, Manisha Jana, M C Sharma, Vaishali Suri, Chitra Sarkar, Sheffali Gulati
Abnormalities of Fatty Acid Oxidation as Potential Candidate Biomarker for Spinal Muscular Atrophy (SMA)
Maina Padmanabha Kava

Neonatal and Fetal Neurology

Head growth, brain growth and neurodevelopmental outcomes in preterm neonates
Thiviya Selvanathan, Vann Chau, Rollin Brant, Anne Synnes, Ruth Grunau, Steven Miller
Myocardial dysfunction as predictor of neurodevelomental outcome in severely asphyxiated term neonates-A case control study.
Himani Bhasin, Arvind Saili, Sushma Nangia
Health Related Quality of Life of Former Preterm Infants after Posthemorrhagic Hydrocephalus and Shunt Insertion
Haim Bassan, Moran Gigi, Jonathan Roth, Rina Eshel, Shlomi Constantini
ROLE OF SUBCORTICAL INJURY IN NEONATAL STATUS EPILEPTICUS
Siddharth Jain
Antenatal diagnosed Arachnoid Cyst [AAC]: An experience of 11 children
Naresh Biyani
Antenatal diagnosed Spilt Cord Malformation type 1 [ASM]: An experience of 18 children
Naresh Biyani
Association of amplitude integrated EEG findings with short term neurological outcome in term neonates
Giriraj Kumar Sharma, Padma Balaji, Vaanathi H, Shobna R, Rahul Yadav
Application of Cerebral Function Monitor for electrical seizure-detection and neurological maturity assessment in Intrauterine Growth Restricted Neonates : A Pilot Study
Jyotindra Narayan Goswami, Ashutosh Kumar, Saroj Kumar Patnaik
Fetal intraventricular haemorrhage (IVH), ventriculomegaly, cataracts and retinal haemorrhages due to Collagen 4A1 mutation
Prakash Satodia, Jerald William, Priya Parthasarathy
Can nuchal cord be responsible for later neurodevelopmental disorders
Edina Karabeg, Enes Karabeg, Adi Karabeg, Biserka Rešić
Why do neonates receive antiepileptics?
Abhijeet Anant Rakshasbhuvankar, Shripada Rao, Soumya Ghosh, Lakshmi Nagarajan
The effect of Fetally Open, Fetoscopic and Postnatal Myelomeningocele Closure on Neuromuscular Outcome in Spina Bifida Aperta
Renate J Verbeek, Agnieszka Pastuszka, Tomasz Koszutski, Johannes H van der Hoeven, Eelco W Hoving, Deborah A Sival
VICI SYNDROME- A RARE CASE REPORT
Giriraj Kumar Sharma, vaanathi H, padma balaji, shobana R, rahul anand yadav
Normative data of ABR in newborns and young infants
monika chhajed, lokesh saini, Vrajesh Udani, Saranjit kaur
A Prospective Observational Study of Neurodevelopmental Outcomes at One Year in Neonates receiving Family Centered Care in NICU
Arti Maria
Long term prophylactic anticonvulsant uses on neurodevelopmental and neurophysiological outcome in asphyxiated neonate with encephalopathy
dipa saha
Neurodevelopmental follow up in high risk babies – The scenario in India
Anasuya Das
Comparison of Developmental Surveillance outcomes of Infants with and without High-risk factors using the ‘Ages and Stages Questionnaire-3’ (asq-3): An Observational Cohort study
pradeep raj balasubramaniam
NEUROIMAGING FINDING OF CONGENITAL CHICKUNGUNYA ENCEPHALITIS
Deepak Dhami
OUTCOME OF ISOLATED FETAL VENTRICULOMEGALY
Prakash Satodia, Soma Mukherjee
Late MR Spectroscopy is not Recommended in the Evaluation of Neonatal Hypoxic Ischemic Encephalopathy (HIE).
Suhasini Kauskal, Christabel Lee, Paola Pergami
SOCS3 a new link between Astrocyte and Fetal Alcohol Spectrum Disorder
Chen Yang
Description of primary neurologic phenotypes in congenital CMV infection
Hitha Vishwanath Amin, Lisa Emrick, Gail Demmler-Harrison
Neurodevelopmental Outcomes of Therapeutic Hypothermia from a NICU in Bangladesh
MA Mannan, AB Shilpi, Naila Z Khan
Characteristics of exosomes in the cerebrospinal fluid of preterm infants
Robert Spaull, Bryony McPherson, Andriana Gialeli, Aled Clayton, James Uney, Oscar Cordero-Llana, Axel Heep

Neurogenetics

Clinical and hereditary characteristics of MECP2 duplication syndrome in Chinese patients
zhanwen he, Xiangyang Luo, Liyang Liang
Cerebral infarction, growth retardation and severe intellectual disability in Korean patients with de novo duplication of 14q32.2
Ji Yoon Han, In Goo Lee
Two Siblings with Congenital Myotonia carrying a New Mutation in the CLCN 1 Gene
Nezir Özgün
Optic Atrophy and Retinal Pigmentary Changes: Expanding The Phenotypic Spectrum of Farber Lipogranulomatosis
Abdullah Saeed Alamri, Ali A AlFaiz, Daniah Alshowaeir, Fatimah Al Mousawi, Adel A Mahmoud, Aqeela Al-Hashim
Expanded clinical spectrum of Okur-Chung neurodevelopmental syndrome in a patient with a hot sport mutation (p.Lys198Arg) in the CSNK2A1 gene. 
Kohei Haraguchi
The Landscape of Genetic causes of basal ganglia and thalamus involvement in children based on the first 5000 MRI studies
SAAD ALSHAHWAN
Delineation of the CLP1 mutations; A possible founder mutation in Turkish cohort
Sema Saltik, Serhat Guler, Tanyel Zubarioglu, Ertugrul Kiykim, Cengiz Yalcinkaya, Gözde Yesil
ISCA2 Related Mitochondrial Disorder: A distinct cause of Infantile Leucodystrophy
Sadia Tabassum, Rowim Al Mutairi, Mohammed Al Mannai, Ali Al Otaibi
Two distinct phenotypes caused by the same mutation in the SAMHD1 gene
Serdal Gungor, Derya Okur, Elmasnur Yilmaz, Ana Topf, Rita Horvath, Hanns Lochmuller, Bilge Ozgor, Ece Sonmezler, Uluc Yis, Ahmet Yaramis, Yavuz Oktay, Semra Hiz
NGS Analysis of four Chinese siblings with Late-Infantile Neuronal ceroid Lipofuscinosis
ren xiaotun
Hereditary sensory and autonomic neuropathy(HSAN ) type IV in Jordan
amira masri
CONSEQUITUR: A multinational effort towards determining the neurogenetic disease burden of consanguineous marriages in Turkey by genomics approaches
Semra Ayse Hiz, Elmasnur Yilmaz, Derya Okur, Ece Sonmezler, İpek Kalafatcilar, Serdal Gungor, Ahmet Yaramis, Uluc Yis, Erhan Bayram, Ana Topf, Rita Horvath, Hanns Lochmuller, Yavuz Oktay
Pallister-Hall syndrome – case report
Himani Bhasin, Suvasini Sharma, Bijoy Patra
The clinical features,laboratories characteristics and genetic diagnosis of Kabuki syndrome
Hong Mei Wang, Xiao-hui Wang, Hu-sheng Wu, Yun Wu, Xiu-wei Zhuo
De novo KCNH1 mutation in an infant with Temple-Baraitser syndrome
Jun Hu
S-adenosylhomocysteine hydrolase deficiency associated with masseter hypertrophy, hyperCKemia, intellectual disability, bradykinesia, cerebellar atrophy, hepatopathy and alterations of creatine and choline homeostasis. Expansion of cerebrohepatomuscular p
Judy Pipo Deveza
Next Generation Sequencing Based Multi-gene Testing of Over 1000 Indian Patients Affected with Neurological Disorders Revealed an Improved (>40%) Diagnostic Yield
Ashraf U Mannan, Aparna Ganapathy, Avshesh Mishra, Anil Vittal Kanthi, Megha Rani Soni, Irene Patric, Aparajit Sridharan, Sobha George, Lakshmi Mohan, Swathi M Chinnappa, Ankitha Prabhudev, Syama Sreedharan, Thyagarajan Chandrasekaran, Priyanka K, Mukunth Sadagopan, Aswathy S L, Vidya H K, Satish Sankaran, Shanmukh Katragadda, Vamsi Veeramachaneni, Ramesh Hariharan, Vijay Chandru
Rett (-like) syndrome: expanding the genetic sprectrum to KIF1A and GRIN1 gene
Jiaping Wang, Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao
Clinical, Genetic and Follow-up Study of Leigh Syndrome in Children
Shen Danmin
NDUFS6 mutations cause lethal neonatal mitochondrial complex I deficiency
MOHAMED ALJABRI
The Clinical Profile of Tuberous Sclerosis Complex: A Retrospective Cohort Study in A Tertiary Care Hospital In Bangladesh
Md Mizanur Rahman, Kanij Fatema
Clinical and Imaging Characteristics of Subependymal Giant Cell Astrocytoma in Patients with Tuberous Sclerosis Complex included in TOSCA – TuberOus SClerosis Registry to IncreAse Disease Awareness
Anna C Jansen, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, Petrus J De Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood
Burden of Illness and Quality of Life among Patients with Tuberous Sclerosis Complex: Findings from TOSCA Research Project
Anna C Jansen, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D' Amato, Guillaume B d'Augères, Petrus J de Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood
Mutation Screening using Next Generation Sequencing (NGS) Gene Panel in Patients with Normal Targeted Metabolic Profiling
MAJED J. Dasouki, Amal Jabr, Ghadah AlDakheel, Mohamed Abouelhoda, Shazia Subhani, Fahd Elbadoui, Nada AlTassan, Dorota Monies
Genetic profile of childhood Charcot-Marie-Tooth disease
Stuart Murray, Joshua Burns, Leah Kim, Kayla Cornett, Manoj Menezes
Phenotype and genotype features of twelve Chinese children with mitochondrial DNA depletion syndromes
Lifang Dai
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport
heba youssef el khashab, Farrukh ABBAS Chaudhry
Aicardi-Goutières Syndrome - expanding the phenotypic spectrum.
Ami Shah, Snehal Mallakmir, Rashid Merchant, Mitusha Verma
X linked infantile epileptic encephalopathy due to SMC1A truncating mutation - ‘An emerging phenotypic syndrome’
Ami Shah, Neeta Naik, Salil Gundewar
A Novel Missense Variant p.(Leu60Pro) in FAM126A Causes Leukodystrophy, Hypomyelinating, 5
Aman Elwadhi, Suvasini Sharma, Bijoy Patra, Parneet Kaur, Katta M Girisha, Anju Shukla
LAMA2 related congenital muscular dystrophies- Two case reports and correlation of genotype with clinical, molecular phenotype
SNEHAL MALLAKMIR, SNEHAL MALLAKMIR, Rashid Merchant, Vijay Yewale
Phenotypic spectrum of Novel mutations in Paediatric mitochondrial disorders: A study from a tertiary care centre in Western Maharashtra.
Dr Sonam Rameshchandra Kothari, Dr Shilpa Kulkarni, Dr Leeha Singh, Dr Anaita Udwadia Hegde, Dr K N Shah
Genotype and phenotype analysis of Leigh syndrome involving valine metabolism in 8 Chinese children
Xiaodi Han, Fang Fang, Zhimei Liu
Genetic spectrum of Infantile epileptic encephalopathy: Indian experience
Spoorthi Jagadish, Rahul Badheka, Neelu Desai, Vrajesh Udani
Collaborative data collection by TREAT-NMD Registries to support post-marketing surveillance in Spinal Muscular Atrophy
Michela Guglieri, Joanne Bullivant, Victoria Hodgkinson, Miriam Rodrigues, Volker Straub, Hugh Dawkins, Craig Campbell, Nathalie Goemans
Clinical and Genetic Correlation in Childhood Onset Pharmacoresistant Epilepsy
Ami Shah, Neeta Naik, Abhinav Sahu, Abhinav Tiwari Tiwari
Top 15 research priorities in tuberous sclerosis complex
Anna Jansen, Eva Schoeters, Alain Wouters, Peter Raeymaekers
Next generation sequencing: a magic bullet or a cautious sword?
Shruti Bajaj, Mamta Muranjan, Anaita Hegde, Mukesh Agrawal
Combining Pathway analysis and animal model behavioral testing for the identification of treatment for neurodevelopmental disorders
Francois Bolduc, Richard He, Kerri Whitlock, Cory Rosenfelt
RHOBTB2 gene: recently discovered cause of rett-like encephalopathy, with possible therapeutic opportunity
Gia Melikishvili, Olivier Dulac, Nugzar Sekhniaidze, Mariam Melikishvili, Sophio Kakabadze, Nazi Tabatadze
ATP1A3 mosaicism in families with alternating hemiplegia of childhood
Xiaoling Yang, Xiaoxu Yang, Shupin Li, Qi Zeng, Jing Zhang, August Yue Huang, Adam Yongxin Ye, Zhe Yu, Sheng Wang, Yuwu Jiang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang
Study of the rare causative genes and analysis of genotype-phenotype correlations of Dravet syndrome
Xiaojuan Tian, Qi Zeng, Jing Zhang, Aijie Liu, Xiaoling Yang, Yuwu Jiang, Xiru Wu, Yuehua Zhang
The Study of Genotype-phenotype Correlation in Patients with Alternating Hemiplegia of Childhood
Shupin Li,, Xiaoling Yang, Jiaoyang Chen, Qi Zeng, Jing Zhang, Yuehua Zhang
Therapeutic Antisense Oligonucleotides based Exon Skipping Gene Editing Strategies in Duchenne Muscular Dystrophy
Arun Shastry
The mosaicism and incomplete penetrance of PCDH19 mutations
Aijie Liu, Xiaoxu Yang, Xiaoling Yang, Qixi Wu, Jing Zhang, Dan Sun, Zhixian Yang, Yuwu Jiang, Xiru Wu, Liping Wei, Yuehua Zhang
HECW2 mutation causes periodic attacks of paralysis, intellectual disability and hypotonia
Kazuyuki Nakamura, Takahiro Abiko, Takashi Kanbayashi, Mitsuko Nakashima, Hirotomo Saitsu, Naomichi Matsumoto, Mitsuhiro Kato
Holoprosencephaly and Kabuki’s syndrome
Surabhi Kaul, Rajan p Patel
A good carpenter loves his tools: a case series highlighting the utility of the newer genetic tests
Shruti Bajaj, Shantala Vadeyar, Mamta Muranjan, Pradnya Gadgil, Kshitij Sheth
A RARE TYPE OF HEREDITARY SENSORY AUTONOMIC NEUROPATHY
PRIYANKA SUNIL WALZADE, SHRUTI AGRAWAL, MANSI SHAH, VIRAJ SANGHI, SANGEETA RAVAT
Developmental delay and cerebellar atrophy due to novel pathogenic variants in Gemin5 gene
Deepa Soundara Rajan
NEUROLOGICAL AND EEG FINDINGS IN ANGELMAN SYNDROME:TALE OF 26 CHILDREN
Jeevan Silwal
Gestalt Diagnosis of Children with Intellectual disability with Dysmorphism- Necessity for Establishing Genetic Diagnostic Approach.
Shaoli Sarker, Mustafa Mahbub, Narayan Saha, AZM AZAM, Humaira Rafiqa Quaderi, Shayla Imam Kanta, Sultana Razia, Fayaza Ahmed, Asma Hoque, Ahmed Asif Ferdous, Naila Zaman Khan
Challenges in diagnosis and management of Acute Necrotising Encephalitis in a large South African family with RANBP2 mutation
Gillian Tracy Riordan, Alvin Ndondo, Sara Seneca, Karen Fieggen, Jo Wilmshurst
CLINICAL PHENOTYPE IN PATIENTS WITH MEF2C MUTATION
Angeles Schteinschnaider, Julia Boccoli, Eliana Julian, Manuel Rivera, Paulina Carullo, Mercedes Villanueva
Cockayne syndrome: Clinical and genetic study of a Maghrebian series
Thouraya Ben Younes, Ichraf kraoua, Hanene Benrhouma, Aida Rouissi, Hedia Klaa, Houda Yaakoub-Youssef, Najoua Miladi, Ilhem Ben Youssef-Turki
Clinical profile, genetic correlation and treatment response in a cohort of children with genetically confirmed Early Infantile Epileptic Encephalopathy (EIEE)
Karthik Muthusamy, Sumita Danda, Sangeetha Yoganathan, Maya Thomas
TELO2 Mutation in a Pair of Siblings -- a Rare cause of Global Development Delay / Epilepsy.
khian aun tan
Subtle Seizure in the form of Recurrent apnoea Beyond Neonatal Period as Initial presentation of DIGEORGE Syndrome –A Rare Case Report .
BASUDEV BISWAL, TUSHITA GHOSH, rachita sarangi, ANUSPANDANA MAHAPATRA
A founder homozygous mutation in VPS53 as the cause of Complicated Hereditary Spastic Paraparesis
Moran Hausman-Kedem, Shay Ben-Shachar, Shay Menascu, Liora Sagie, Aviva Fattal-Valevski
Diagnostic yield of clinical exome sequencing in non-structural infantile onset epileptic encephalopathy
Prashant Jauhari, Prabhjot Kaur, Aparajita Gupta, Biswaroop Chakrabarty, Sheffali Gulati
Assessment of cardiac involvement in childhood Neurofibromatosis Type 1 diagnoses, identification of Rasopathic cases
Ilyas Emre Tekdemir, Deniz Yüksel, Vehbi Dogan, Ayşe Aksoy, Hulya Kayılıoglu, Ulkuhan Oztoprak, Erhan Aksoy, Cigdem Sel
Hereditary spastic paraplefgia (HSP) in Brazilian children: a clinical and genetic study.
Roberta Magalhães Ortega, Marcondes Cavalcante França Jr., Sergio Rosemberg
A novel AP1S2 gene splice site mutation of X-linked mental retardation in a Chinese pedigree and literature review
Liang Huo
Clinical and Genetic Spectrum of Disorders with Cerebellar Atrophy
Ramya Bandi, lokesh lingappa, Prasanthi Aripirala, Rini Kothari, Ramesh Konanki, Nikit Milind Shah, Smilu Mohanlal, Thenral SG, Ramprasad VL
Copy Number Variant Sequencing reveals a 10q24.31-q24.32 haploid duplication in a Chinese family with congenital Split hand/foot malformation
LI GAO
Mutation Analysis of genotype and clinical phenotype in children with hyperinsulinemic hypoglycemia
LI GAO
Neuropsychological and behavioral characteristics of children with a candidate mutation in EMC10 - The characteristics of a new syndrome?
Eliana Haddad Eid, Tammy Pilowsky Peleg, Rachel Straussberg
Modeling vanishing white matter disease with patient-derived induced pluripotent stem cell reveals astrocytic dysfunction
Ling Zhou, Peng Li, Na Chen, Lifang Dai, Yinan Liu, Li Shen, Jingmin Wang, Yuwu Jiang, Ye Wu
Dysmorphology leading to the diagnosis of Schwartz Jampel Syndrome
Jayarekha Raja
AicardiGoutieres - A close mimick of congenital infection: Case series with 3 children and 4 families
Beena Suresh, Sujatha Jagadeesh, Vaishnavi Reddy, Min Lee-Kirsch
Novel homozygous mutations in NARS2 gene with mitochondrial dysfunction presenting as early infantile epileptic encephalopathy
Wilson Heredia
Natural history and genotypic spectrum of cavitating leukoencephalopathy in childhood
Jie zhang, Ming Liu, Zhongbin Zhang, Ling Zhou, Weijing Kong, Yuwu Jiang, Jingmin Wang, Jiangxi Xiao, Ye Wu
A study on protective effect of BDNF-MSC in Rett syndrome model
Hyo Jeong Kim, Jaesuk Lee, Delger Bayarasaikhan, Bonghee Lee
Clinico-investigative profile of Hereditary spastic paraplegia in children
Mayank Vrujlal Detroja, Mahesh Kamate
“STUDY OF CLINICO-ETIOLOGICAL PROFILE OF EARLY ONSET EPILEPTIC ENCEPHALOPATHY IN CHILDREN’’
Boda Praful Kumar, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, RADHA RAMA DEVI, PRASHANTHI ARIPIRALA, THENRAL SG
Whole Exome Sequencing in Diagnose of Patients with Leukodystrophy
Hsin Pei Wang, Wang-Tso Lee
TITLE: Status of Genetic Counselling in Hereditary Neurogenetic disorders: A clinic-epidemiologic study in Western Rajasthan
Ankit Manoj Panday
The spectrum of clinical findings, radiological profile and genetics of Vanishing White Matter Disease from tertiary care center of Southern India.
Syed Shah Naseeruddin Sarmast
Developmental delay and cerebellar atrophy due to novel pathogenic variants in Gemin5 gene
Deepa Soundara Rajan
Reanalysis of the whole exome sequencing raw data and the clinical information can yield additional diagnosis missed by previously commercial genetic test report in children with epilepsy and intellectual disability
Jinliang Li, Kai Gao, Yuwu Jiang
TITLE: Spectrum of Neurocutaneous Disorders in Pediatric Neurology Clinic in Western Rajasthan
Ankit Manoj Panday
Whole Exome Sequencing (WES) identifies PGAP3 mutation in three patients from two Saudi families with hyperphosphatasia with mental retardation syndrome 4 (HPMRS4)
ELSAYED MOHAMED ALI, HAMOUD MOHAMED GALLAB
Infantile Neuroaxonal Dystrophy (INAD) in a Pair of Malaysian Siblings with Progressive Cerebellar Atrophy
Limin Li, Meow Keong Thong, Chee Geap Tay, Choong Yi Fong
Rare chromosomal causes of developmental delay and epilepsy- Experience from a tertiary care center
Chaitanya Ashok Datar
Preempting complications in genetic disorders: Lowe Syndrome a case study
Priyanka Dilip Patil
Clinical and genetic studies on fifteen patients with tyrosine hydroxylase deficiency
Yao Zhang
Juberg-Hellman Syndrome :X linked female restricted epilepsy in an extended family in North Kerala
Anilkumar Elayadeth, Divya Pachat, Akbar Mohamed
Diversity of phenotypes in Infantile Seizure and their families with PRRT2 Mutations
TUNG MING CHANG, Inn Chi Lee, Ming Chen, Yuh Jyh Jong
Phenotype plays an important role in the genetic diagnostic success rate in a cohort of 500 families with rare
Keri Ramsey
XIA-GIBBS SYNDROME WITH PARTICULAR HAIR - A RARE CAUSE OF GLOBAL DEVELOPMENTAL DELAY
Diana Gabriela Barca, Cristina Minca, Mihaela Axente
CHALLENGES IN CLINICAL INTERPRETATION OF NEW MUTATIONS IN RARE CONDITIONS
Diana Gabriela Barca, Sorina Mihaela Papuc, Carmen Burloiu, Aurora Arghir, Magdalena Budisteanu
Molecular diagnosis and genetic counselling of X fragile Syndrome
Nouha Abdelmoula Bouayed, Sonda Kammoun, Fatma Abid, Balkiss Abdelmoula, Wafa Aloulou, Samir Aloulou

Neurocritical care, Neurotrauma, Neuroprotection

Neurological Complications in Pediatric Cardiac Surgery: Incidence, Predictors and Outcome
wejdan salem hakami
Our experience in the management of diffuse axonal injury patients in pediatric population and the review of literature- an institutional study.
Achal Gupta, Konika Bansal, Nitin Dange
Assessment of clinical follow-up and prognosis in acute neurological condition in pediatric patients managed in pediatric intensive care unit
Ece Naz Karakaya, Deniz Yüksel, Selman Kesici, Ayşe Aksoy, Ülkühan Öztoprak, Çigdem Genç Sel, Erhan Aksoy, Hülya Kayılıoğlu
Emergency room visits and admission rates of children with neuromuscular disorders: A 10-year experience in a medical center in Taiwan
Tai-Heng Chen, Yao-Hua Liu, Wei-Tsun Kao, Yung-Hao Tseng
Diagnostic Utility of Middle Cerebral Artery flow indices as a Non-invasive tool for detecting Raised Intracranial Pressure in Pediatric patients.
Indar Kumar Sharawat, Naveen Sankhyan, Ananthanarayanan Kasinathan, Arun Bansal, Jitendra Kumar Sahu, Kushaljit Singh Sodhi, Mangat Ram Dogra
Clinico-radiological profile of acute leucoencephalopathy with restricted diffusion- a novel cause of acute encephalopathy in children.
Mahesh Kamate
Early Post-Traumatic Seizures in PediatricTraumatic Brain Injury
Snehal Surana, Arpita Devbrata Adhikari, Vineet Kumar, Mona Gajre, Vidya M
Big Black Brain
Sayoni Roy Chowdhury, Rajwanti K Vaswani, Chandrahas Deshmukh, Jane David, Anupa Johny Ekka
Native medicine use and lead poisoning in children
Renee Alce, Renee Alce, Padma Balaji, Ravikumar Krupanandan, Venkataraman Viswanathan, Bala Ramachandran
Neuroprotective effects of vitamine D in hiperoxic brain injury
erhan bayram, ipek polat, serap cilaker mıcılı, Meryem Calısır, Uluç Yiş, Guven Erbil, Osman Yılmaz, semra hız kurul
A prospective study on incidence of non-convulsive status epilepticus in children with acute encephalopathy
sruthi thiruveedi, Dr Lokesh Lingappa, Dr Ramesh Konanki, Dr Nikit shah, Dr Anupama yerra, Dr Farhan Shaikh
Brain Death Determination for Comatose Patients in The Pediatric Intensive Care Unit
Kun-Long Hung, Su-Ching Hu, Wong Lee-Chin

Neuroradiology

Cranial Magnetic Resonance Imaging patterns in infants with hypernatremic dehydration
Gouri Rao Passi, Shailesh Gupta, Puneet Yadav
Congenital Brain and Spine Malformations – prenatal fetal MRI approach
Ivana Markovic
Value of Neuroimaging in Thalassemia
Amitkumar Jayant Choudhari, Rashid Merchant, Deepak Patkar, Mitusha Verma, Alka Karnik
pseudo TORCH syndrome – Recessive mutation in occludin ( OCLN ) gene
shriganesh patil
Intracerebral large artery disease with Aicardi-Goutières Syndrome
Chung Jane Ng, Wang Tso Lee
Role of Fetal Neuroimaging in Congenital Cytomegalovirus Infection, with Postnatal Imaging Correlation.
Vinay Kandula, Rahul Nikam, Lauren Averill, Arabinda Choudhary
Clinical & Neuro-Imaging Changes of Subacute sclerosing panencephalitis- Experience 30 Cases in Tertiary Care Center in Bangladesh
Gopen Kumar Kundu
Case Report: Van der Knaap Disease
Vaishali Deshpande, Vaishali Deshpande, Sushma Save, Sandeep Bavdekar
NCL11:A rare cause of pure pancerebellar atrophy
Mahesh Kamate
Distribution of Cerebellar Tonsillar Position in the Indian Pediatric Population
Divyata R Hingwala
Neuroimaging findings in Neuromyelitis Optica spectrum disorder and mimics
Divyata R Hingwala
Brain MRI in children with Wilson Disease
yuan wu, Ying Zhu, Ting Zhang, Ming Li
Isolated mitochondrial complex IV (cytochrome c oxidase) deficiency mimicking ADEM
Amal Yousef Kentab, Mohammed Al-Nasser, Hamdy Hassan, Hisham El Khaldi
Neuroimaging in paediatric central nervous system infections.
Dr.Deepak Patkar, Dr. Amitkumar Choudhari, Amit kumar Pandey, Dr. Shilpa Kulkarni, Dr. Rashid Merchant
Pituitary iron and volumetric analysis in β Thalassemia
Dr. Anuja Nayak, Dr. Deepak Patkar, Dr. Amitkumar Choudhari, Dr. Shilpa Kulkarni, Dr. Rashid Merchant
cerebellar calcification and seizures in a child with autoimmune polyendocrine syndrome 3A
Rachel Peterson, Asha Kuruvilla, Ann Mathew
Clinical & Neuro-Imaging Changes of Subacute sclerosing panencephalitis- Experience 30 Cases in Tertiary Care Center in Bangladesh
Gopen Kumar Kundu
Vacuolar leukodystrophy revealing COX10 mutation
Thouraya Ben Younes, Hanene Benrhouma, Rania Ben Aoun, Lilia Kraoua, Said Galai, Hedia Klaa, Aida Rouissi, Ridha Mrad, Cyrine Drissi, Souhail Omar, Abdelhamid Slama, Ichraf Kraoua, Ilhem Ben Youssef-Turki
Spectrum of acquired White Matter Disorders in Children and their Outcomes
Vikas Chauhan, Arushi Gahlot Saini, Naveen Sankhyan, Sameer Vyas, Paramjit Singh, Jayashree Muralidharan
Pineal cysts in children: the experience of child neurology department
sirine belghuith
RHOMBENCEPHALO SYNAPSIS – A RARE CEREBELLAR ANOMALY WITH GOMEZ LOPEZ HERNANDEZ SYNDROME
Leema Pauline Cornelius
ne imaging of children with Tuberous sclerosis complex: is it safe to adapt international recommendations for resource limited settings?
Marie Wessels, Bergit Schlegel, Jo M Wilmshurst
ALERD In a Post-Operative Case Of a 20 Month Girl Child.
Narendranadha reddy k, MAHESH KAMATE, MAYANK DETROJA, santosh kurbeit
The spectrum of leukodystrophies in children: Experience at a tertiary care centre from North India
Biswaroop Chakrabarty, Priyanka Madaan, Puneet Jain, Sachendra Badal, Prashant Jauhari, Atin Kumar, Manisha Jana, Neerja Gupta, Madhulika Kabra, Sheffali Gulati
Clinical correlates of mineralizing lenticulostriate vasculopathy (mLSV) in children
Jatinder Singh Goraya
POMS 2b pediatric cohort): Effect of Auto-adjusting Continuous Positive Airways Pressure on cognition and MRI in children with Sickle Cell Disease: a single-blind, randomized, controlled phase II trial
Satwinder Sahota, Jamie Kawadler, Hanne Stotesbury, Melanie Koelbel, April Slee, Dawn Saunders, Fenella Kirkham

Neuroimmunology

Autoantibodies normilize after a month in tonsilitis and persist in Sydenham's chorea
Hilla Ben-Pazi, Julie Stoner, Adi Aran, Kathy Alvarez, Madeleine W Cunningham
Efficacy of thyrotropin releasing hormone therapy for patients with subacute sclerosing panencephalitis
Eiji Nakagawa
A NEW NEUROINFLAMMATORY DISORDER IN CHILDREN: Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
tarishi nemani, PURVA KENI KARNAVAT, EPARI SRIDHAR, ANAITA UDWADIA HEGDE
MicroRNA-181a-5p regulates blood brain barrier permeability after meningoencephalitis via positive regulating HMGB1 expression
Ling-juan Liu
Unsolved mystery:11-year-old patient with antibody negative immune-mediated necrotizing myopathy
Cemal Karakas, Jeetendra Sah, Yaacov Anziska, Yoshimi Hisamoto, Radha Giridharan, Joan Cracco, Alexandra Reznikov, Geetha Chari
Paediatric Guillian-Barré Syndrome variants presenting with dysautonomia
Omar Abdel-mannan, Luigi D’Argenzio, Matthew Pitt, Felice D’Arco, Sanjay Bhate, Yael Hacohen, Marios Kaliakatsos
Hemophagocytic Lymphohistiocytosis: A missed diagnosis in children with neurological manifestations
Marwa Saeed Abd Elmaksoud, Ahmed Adel Hassan Elbehairy, Asmaa Elsharkawy, Yasmine El Chazli
Anti-MOG antibody related demyelinating diseases: Clinical-radiological spectrum and treatment experience
Hepsen Mine SERIN, Erdem Simsek, Seda Kanmaz, İpek Dokurel Cetin, Sanem Yılmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben
Clinical and prognostic analysis of ocular myasthenia gravis in children
Chen Jiji, Jiang Li, Li Xiujuan, Hong Siqi
clinical features of Myelin oligodendrocyte glycoprotein(MOG)antibody positive cetral nervous system inflammatory dymyelination in 31 children
Zhang wh
Therapeutic plasma exchange in inflammatory demyelinating CNS syndromes in paediatric patients
Silvia Noemi Tenembaum, Andrea Savransky, Marina Huaman Rios, Silvana Liz Vergel, Mabel Castro Velasquez, Sara Perez Sierra, Gabriela Marcarian, Romina Alba, Ana Maria Pugliese
Effect of fingolimod in pediatric MS: further insights from sensitivity, supportive and post-hoc analyses from PARADIGMS
Kumaran Deiva, Peter Huppke, Brenda Banwell, Tanuja Chitnis, Jutta Gärtner, Lauren Krupp, Emmanuelle Waubant, Tracy Stites, Gregory Lewis Pearce, Martin Merschhemke
OPSOCLONUS-MYOCLONUS SYNDROME: SIMULTANEOUS COMBINATION IMMUNOSUPPRESSIVE THERAPY WITH EXCELLENT OUTCOME
Shailesh Barot, Anaita Hegde, Krupa Torne, Manohar Patil, Vaibhavi Barot
FATAL DIAGNOSIS OF SSPE TO TREATABLE CAUSE OF AUTOIMMUNE ENCEPHALITIS
chandra sadanandavalli retnaswami
Improved performance of the 2017 McDonald criteria for diagnosis of multiple sclerosis in children irrespective of age
yael hacohen, Wallace Brownlee, Kshitij Mankad, WK 'Kling' Chong, Ming Lim, Evangeline Wassmer, cheryl Hemingway, Fredrik Barkhof, Olga Ciccarelli
Pediatric-onset multiple sclerosis in Egypt: a multi-center registry
AMR MOHAMMED
Spinal cord disease following Falls and minor Sporting injury: Myelitis or SCIWORA?
Terrence Thomas
case series of pediatric multiple sclerosis
Yareeda Sireesha, Angamattu Kanikannan, Mathukumalli Neeharika
Inflammatory neuropathology of infantile Alexander disease: A case report
Kengo Kora, Takeo Kato, Minako Ide, Takayuki Tanaka, Tomokatsu Yoshida
Iatrogenic Intracranial Hypertension secondary to Immunoglobulin therapy of Chronic Inflammatory Demyelinating Polyneuropathy
Elizabeth Pilley, Conrad Schmoll, Jayakara Shetty, Kenneth McWilliam
Pediatric Acquired Demyelination Syndromes (ADS) profile in a Brazilian center
José Albino da Paz, Renata Paolilo, Samira Apostolos-Pereira, Dagoberto Callegaro, Ana Luiza Araújo, Douglas Sato, Carolina Medeiros Rimkus
Acquired neuromyotonia in children with CASPR2 antibodies
SNEHAL SURANA
Subacute meningitis / Prolonged fever as presentations of MOG antibody associated autoimmune demyelination syndrome – a case series
Rahul Badheka, Vrajesh Udani, Neelu Desai
AUTOIMMUNE ENCEPHALITIS: OUTCOMES IN A PEDIATRIC POPULATION
MONICA elsa FERREA, Paola Di Lalla, Laura Silvina Fernandez, Silvia Intruvini
Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive To Steroids (CLIPPERS)
Manish Prasad
Pediatric autoimmune encephalitis: Case series from two Chinese tertiary pediatric neurology centers
Jianzhao Zhang, Yuwu Jiang, Jianzhao Zhang
Rare cause of intractable vomiting: Neuromyelitis Optica
Reena Jain, nirupa chandorkar, dinesh raj, pankaj vohra, suvasini sharma
Retrospective study of 30 patients with Opsoclonus-Myoclonus Syndrome (OMS) in Brazil.
José Albino da Paz, Renata Paolilo, Ciro Matsui
Clinical profile and outcome of Acute Necrotizing Encephalopathy of Childhood (ANEC): a retrospective cohort study from a tertiary care centre of North India
Sachendra Badal, Prateek Kumar Panda, Priyanka Madaan, Ankita Pal, Prashant Jauhari, Biswaroop Chakrabarty, Vishal Sondhi, Rachana Dubey, Sheffali Gulati
Clinical and Neuroradiological profile of Acute Disseminated Encephalomyelitis in 13 children at tertiary center in Saudi Arabia
Amal Yousef Kentab, Amal Y. Kentab, Mustafa AM. Salih, Hamdy H. Hassan, Mohammed Na N. Al-Nasser, Heba Y. El khashab
Intravenous immunoglobulin versus methyl prednisolone in children with ADEM:: a randomized controlled trial
Rajniti Prasad, Gautam Goswami
Pediatric anti-NMDA receptor encephalitis: experience of a tertiary care teaching center in North India
Biswaroop Chakrabarty, Prateek Kumar Panda, Prashant Jauhari, Vishal Sondhi, Rachana Dubey, Sheffali Gulati
Clinico-epidemiological profile of Opsoclonus Myoclonus Ataxia syndrome: experience of a tertiary care centre from north India
Biswaroop Chakrabarty, Prabhjot Kaur, Prashant Jauhari, Vishal Sondhi, Rachana Dubey, Prateek Kumar Panda, Sheffali Gulati
Spectrum of Guillian Barre syndrome in children – atypical features, types, prognostic indicators and relationship to zika virus.
Ishita Tewari, Chandrakanta Kumar, Ravindra Garg, Amita Jain, Rashmi Kumar
The case of Kinsburn`s Encephalopathy in a child with neuroblastoma of posterior mediastinum
Tetiana Stetsenko
Pathognomonic features and Neuropsychiatric Outcome of Anti-NMDAR Encepahlitis in children: A case series
Janaki Menon, Veena Nair, Purushothaman Kuzhukkathukandiyil
Brain stem encephalitis in children
Kavita P Thakkar, Yoshimi Sogawa, Amy C Goldstein, Giulio Zuccoli
Our experience with Rituximab in two patients with anti-MuSK positive Myasthenia gravis.
MESUT GUNGOR, BULENT KARA, AYFER SAKARYA GUNES
Follow-up Study on Chinese children with relapsing MOG-IgG-associated Central Nervous System demyelination
Ji Zhou, Xiaopeng Lu, Yao Zhang, Taoyun Ji, Yiwen Jin, Min Xu, Yuehua Zhang, Xinhua Bao, Hui Xiong, Xinzhi Chang, Yuwu Jiang, Ye Wu
Clinico-radiological correlation of Acquired Demyelination Syndromes(ADS) of central nervous system: A pediatric cohort
ANSHITA ARORA, SONAM KOTHARI, SHILPA KULKARNI, ANAITA HEGDE, KRISHANKUMAR SHAH
Intracranial Calcification, Spastic Paraparesis, Length Shortening and Immunological Disorders: Three SPENCDI Cases
MESUT GUNGOR, AYFER SAKARYA GUNES, BULENT KARA
Acquired Central Nervous System demyelinating syndromes in children: experience of a tertiary centre from North India
Priyanka Madaan, Biswaroop Chakrabarty, Prateek Kumar Panda, Juhi Gupta, Vishal Sondhi, Rachana Dubey, Atin Kumar, Manisha Jana, Sheffali Gulati
Acquired neuromyotonia in children with CASPR2 antibodies
Snehal Surana, Ratna Kumar, Prab Prabhakar, Matthew Piit, Yael Hacohen, Sukhvir Wright
Clinico-radiologic spectrum and outcome of pediatric demyelinating disorders – A retrospective study
Bidisha Banerjee, Muhammed Valikandy Hafis, Ullas V Acharya
Long term Outcome of Thymectomy in Pediatric Myasthenia Gravis
leeha Singh, Leeha Singh, Shilpa Kulkarni, Anaita Hegde, K. N. Shah
Opsoclonus myoclonus ataxia syndrome: A study from a tertiary care center in Western India
leeha Singh, Shilpa Kulkarni, Anaita Hegde, K. N. Shah
Low seropositivity to antiganglioside antibodies in Guillain-Barre Syndrome; A Prospective study of 83 children
Naveen Sankhyan, Sunit Singhi, Pratibha Singhi, Savita Verma, Mini Tageja
Use of the radiotracer 18F-GE180 for PET scan imaging of active neuro-inflammation in children with multiple sclerosis
Badal G Jain, Hua Li, Zhang Shaohui, Xuyi Yue, Rahul Nikam, Alana Salvucci, Yangchun Xin, Diane Chugani, Harry Chugani
Familial acute necrotizing encephalopathy (ANE1)
Zoltan Liptai, Sarolta Dobner, Peter Benke, Anna Szocs, Judit Moser, Fleur Vansenne
Anti NMDAr antibody mediated encephalitis: unusual presentation with focal motor deficits: 2 case reports
pradnya gadgil, Nilima Bhalerao, Sunita Venkatraman
Role of Rituximab and pulse Cyclophosphomide in anti-NMDAR encephalitis
Lakshminarayanan Kannan
CLINICAL PROFILE, TREATMENT AND OUTCOME IN CHILDREN WITH NMDA RECEPTOR ENCEPHALITIS: DATA FROM A TERTIARY CARE MEDICAL COLLEGE IN KERALA.
abhishek ravindra jain, mini sreedharan, P A Mohammed Kunju, mary iype, bindu thankappan, ishita deasi, rajagembeeran venugopal, priyanka ramteke, heena sheikh
Radiologically isolated syndrome in childhood: experience of our clinic
Ayfer Sakarya Güneş
The Clinical Course of Children Younger than 7 Years of Age with Anti-N-methyl-D-aspartate Receptor Encephalitis
Hitha Vishwanath Amin, Sarah R Risen, Mered Parnes, Christian Michael Niedzwicki, Eyal Muscal

Neurosurgery

Feasibility of using transcranial magnetic stimulation (TMS) for presurgical language mapping in young children
Shalini Narayana, Katherine K Schiller, Luke M Embury, Stephen Fulton, Amy McGregor, Basanagoud Mudigoudar, Sarah Weatherspoon, James W Wheless, Frederick Boop
Dermoid cyst mimicking Gastro esophageal reflux disease
Surabhi Kaul, Stephen Katzen, Andrew Minzenmayer, Andrew Fang, Nivedita Thakur, Manish N Shah, Rajan P Patel
Acalvaria: a 5-months follow up
Ivan Riyanto Widjaja, Angelina Armine Susanto Putri, Dicky Adi Putra, Marsha Zaneta, Nur Hasan
Infected Dermal Sinus with Arachnoiditis (IDSA): An experience of 20 children
Naresh Biyani
Functional mapping of the brain by novel tripolar EEG electrodes
Sameer C Dhamne, Damon Hyde, Shunan Li, Walt Besio, Alexander Rotenberg
International Infant Hydrocephalus Study (IIHS): 5 year health outcome results of a prospective, multicentre comparison of endoscopic third ventriculostomy (ETV) and shunt for infant hydrocephalus
YAEL LEITNER
Utility of neuronavigated transcranial magnetic stimulation (nTMS) for functional motor mapping in infants and toddlers
Harper Lee Kaye, Gabrielle Block, Saeed Kayhanian, Hannah Purtell, Ugur Damar, Alexander Rotenberg

Neurooncology

A randomized, double-blind, parallel group, placebo-controlled trial of metformin in tuberous sclerosis complex
Sam Amin, Andrew A Mallick, Hannah Edwards, Andrew Lux, Amjad Khan, Matthew Laugharne, Marcus Likeman, Finbar O'Callaghan
The neurological manifestations of lympho-haematopoietic malignancies
Dr Sonam Rameshchandra Kothari, Dr Shilpa Kulkarni, Dr Meghana Nadiger, Dr Anaita Udwadia Hegde, Dr K N Shah
THE СLINICAL CASE OF TOXIC CRANIAL NEUROPATHY IN A CHILD WITH NEUROBLASTOMA
Akmal Asatullayevic Mukhamedov

Neuro-opthalmology

Congenital double elevator palsy with ptosis in a child
Subramanian Velusamy, Subramanian Velusamy, Balaraman Krishnakumar, Balasubramanian Radhakrishnan, Rajendran Abinaya, Kandasamy Sivakumar, Kandasamy Sivakumar
Cerebral vision impairment in children: How much of it is preventable?
Ramesh Konanki, Sravanthi Kuruva, Lokesh Lingappa, Nikit Milind Shah, Srikanth Domala
Neurodevelopmental disorders and disordered chromatin remodeling: the lessons from Rubinstein–Taybi syndrome spectrum and clinical presentation of a Tunisian case revealed on behalf of bilateral congenital glaucoma and other ocular abnormalities
Nouha Abdelmoula Bouayed, Sonda Kammoun, Fatma Abid, Wafa Aloulou, Samir Aloulou

Neurorehabilitation

Intensive Neurophysiological rehabilitation system (INRS)- new approach for treatment of children with Autism
Volodymyr Kozyavkin
Effects of tDCS and HD-tDCS on motor learning and motor maps in children
Adrianna Giuffre, Lauran Cole, Patrick Ciechanski, Helen Carlson, Ephrem Zewdie, HsingChing Kuo, Cynthia Kahl, Amy Webber, Megan Metzler, Ashley Harris, Adam Kirton
Mirror Therapy in children with hemiplegia: a comparative study
Neha Ahuja, Gouri Rao Passi
Retrospective analysis on ayurvedic treatment protocol in cerebral palsy children.
Deepty Nair, Dr Dinesh K S
Impairment of neurological ontogenesis in children with autism spectrum disorders: cohort study
Taras no Voloshyn
Early Therapy in Perinatal Stroke (eTIPS): Feasibility Trial
Anna Purna Basu
Long Term Outcomes of Patients with Functional Neurological Disorders
Charoula Siafaka, Vanita Shukla, Anirban Majumdar, Biju Hameed
DISORDERS OF CONSCIOUSNESS IN PEDIATRIC BRAIN INJURED PATIENTS: OUTCOMES
MONICA elsa FERREA, Flavia Dorrego, Silvia Intruvini
Effect of aerobic training on muscle endurance among adolescents with bilateral spastic cerebral palsy.
Ehab Anwar Waly, Ahmed Mostafa Aboeleneen, Ashraf Darwesh
Factors affecting adherence to a home program: a survey presenting to a tertiary care unit.
Franzina Coutinho, Akansha Shah, Shantanu Tilak, Neelu Desai
Neurorehabilitation in children with acquired brain injury: Does multidisciplinary and holistic approach lead to equitable perceived outcomes irrespective of ethnicity, injury type or severity?
Amit Bali, Kayleigh Goddard, Gerard Anderson, Vivek Mundada
Model of Integrated Support for the families of the children with traumatic brain injury: experience of one centre
Vivek Mundada, Gerard Anderson, Theresa Pass
Speech & Swallowing rehabilitation in Child with GBS: The journey from ICU to School
abhijeet vilas botre

Neuroendocrinology

Effect of Glucocorticoid Receptor’s Function on Expression of MAOA by GC-KLF11-MAOA Pathway
Yanhui Chen, Jie Zheng, Xiaoxia Lin, Jun Hu

Stroke & Neurovascular Disorders

A RARE COMPLICATION OF NEPHROTIC SYNDROME IN PEDIATRICS - ISCHEMIC STROKE
NEHA MANJHANI, SAKSHI SHARMA, RAVI SHARMA, RAJIV BANSAL, VIVEK JAIN
Comorbidity of Myhre syndrome and Moyamoya disease: a case report and literature review
qun li Liu, juan ling Liu, an ding Mao
RNF213 mutation in child with DMD carrier combined with Moyamoya disease
Ji Yoon Han, Yun Tae Lee
Anatomical Venous Variants in Children with Cerebral Sinovenous Thrombosis (CSVT):
Elizabeth Kouzmitcheva, Andrea Andrade, Prakash Muthusami, Manohar Shroff, Mahendranath Moharir
A Case Series of Acute Necrotizing Encephalopathy of Childhood
Reza maskani, Farzad Ahmadabadi, Sonia Ruhollahi, Adel Ahadi, Shamal maskani, Sonia hosseini anbaran
Mineralizing Angiopathy- A case series of 5 cases.
Anand GAJAJNAN DIWAN
Cerebral Sinovenous Thrombosis in Children: Single Center Experience
İpek Dokurel Cetin, Hepsen Mine SERIN, Cenk Eraslan, Erdem Simsek, Seda Kanmaz, Sanem Yilmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben
Validation of Cerebrovascular Reactivity Imaging in Children
Kenda Alhadid, Jackie Leung, William Logan, Nomazulu Dlamini
LONG-TERM FUNCTIONAL AND COGNITIVE OUTCOMES AFTER PEDIATRIC STROKE
Shaanvar Sh Shamansurov, Sadokat O Nazarova, Parviza T Usmanova, Nodirakhon M Tulyaganova
Thalamic diaschisis following perinatal stroke and its relationship to clinical motor function
Brandon Craig, Helen Carlson, Adam Kirton
Pediatric ischemic stroke associated to deficiency of adenosine deaminase 2 (DADA2).
José Albino da Paz, Tayrine Gonçalves, César Alves, Leandro Lucato
Utility of Testing for Prothrombotic Disorders in Children with Perinatal Periventricular Venous Infarction
Noa Mandel-Shorer, Daune MacGregor, Suzanne Laughlin, Leonardo Brandao, Gabrielle deVeber, Nomazulu Dlamini, mahendranath moharir
Multiple Burr Holes [MBH] as a surgical revascularization procedure for Moyamoya disease [MMD]: An experience of 9 children
Naresh Biyani
Factors influencing long term outcomes in childhood arterial ischemic stroke
Maggie LoYee Yau, Jay Gajera, Anneke Grobler, Belinda Stojanovski, Mark MacKay
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