Presentations and Authors


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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
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
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
Sleep Disorders in Children with Cerebral Palsy
Tanmay Sanjay Jadhav, Dr. Shilpa Kulkarni, Dr. Amit Bhondve
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
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
Solution to problem of Plenty
Rahul Bharat
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
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

CNS Infections

Congenital Zika syndrome and infatile spasms - case series study
Lucas Victor Alves, Maria Júlia Gonçalves Mello, Patrícia Bezerra, João Guilherme Bezerra Alves
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
Atypical CNS infection: needs a mention.
abhijeet vilas botre
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
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
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
SSPE mimicking anti-NMDA receptor encephalitis
Shilpa Devamare, Vikram Bhaskar, Himani Bhasin, Suvasini Sharma
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
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
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

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
All work and no play: The relationship of leisure time activities and psychological disorders in school children
Pallavi Bhad, Gouri Rao Passi
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
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
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
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

Epilepsy

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
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
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
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
Lacosamide responsive ESES (electrical status epilepticus in slow wave sleep )– 2 case reports
pradnya gadgil, Nilima Bhalerao, Sunita Venkatraman
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
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
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
Prevalence and association of risk factors for anticonvulsant polytherapy amongst epileptic children: A case-control study
Shifa Bidhan, Krishna M Adhikari, Rakesh Kumar Gupta
Experience of ketogenic diet as an adjuvant therapy in Febrile Infection Related Epilepsy Syndrome (FIRES)
Purnima Suhas Prabhu, Vrajesh Udani, Toral Bhatt, Neelu Desai
The role of sleep and awake EEGs in detection of epileptiform discharges in pediatric population.
Nupur Sinha, Shilpa Kulkarni, Suresh Birajdar, Tushar Maniar
COMPARISON OF CALCIUM LEVELS IN CHILDREN WITH FEBRILE SEIZURES AND CHILDREN WITH FEVER AND NO SEIZURES
Rekha Mittal, Shailabh Gupta, Naresh Bhatia
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
PHOTOSENSITIVITY AND CLINICAL CHARACTERISTICS FROM A SCOTTISH POPULATION COHORT
Gareth Neo, Lauren Marie Smith, Leanne Brennan, Jay Shetty, Krishnaraya Kamath Tallur
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
Retrospective cohort of Dravet syndrome due to SCN gene mutation from Southern India
Hemadriben Muljibhai Vegda, Vykuntaraju Gowda, Raghavendraswami Amoghimath, Asha benakappa
EPILEPTIC ENCEPHALOPATHY DUE TO GABRG2 MUTATION
Angeles Schteinschnaider, Isaura Gonzalez, Eliana Julian, Julia Boccoli
A hot and jerky child
Sonal Bhatia
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
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
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
LANGUAGE EVALUATION IN GENETIC EPILEPSY FEBRILE SEIZURES + SYNDROME – A PROSPECTIVE CONTROLLED OBSERVATIONAL STUDY
Toral Bhatt, Vrajesh Udani, Megha Shah, Neelu Desai, somini mehta
Clinical Profile of Epilepsy in Neonatal Hypoglycemic Brain Injury.
Madhavi Shelke, Shirish Bhartiya, Varsha Vaidya, Sandeep Saraf
Febrile Infection Related Epilepsy Syndrome (FIRES) – A rare cause of super refractory status epilepticus
Aanchal Pradeep Khemani, Sanjay Bafna, Sagar Lad, Nandan Yardi
“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
Polypharmacy in childhood epilepsy syndrome management: overuse or underuse of a diagnostic tool?
selina husna BANU, SELINA HUSNA BANU, Naila Zaman KHAN
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

Metabolic Disorders

A RARE CAUSE OF STRIDOR & RECURRENT CENTRAL APNEA: MAPLE SYRUP URINE DISEASE
RAVI SHARMA, SAKSHI SHARMA, VIVEK JAIN, LALIT BHARADIA
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
Fatal neonatal lactic acidosis secondary to a novel defect in COX16 causing complex IV deficiency
Maina Padmanabha Kava, Shanti Balasubramaniam, Barry Lewis, Richard Rodenburg
A rare cause of developmental delay
Sakshi Batra, Aman Elwadhi, Suvasini Sharma, Bijoy Patra
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
CONGENTIAL METHEMOGLOBINEMIA TYPE 2: A RARE CAUSE OF NEURODEVLOPMENTAL DELAY
vishal bhansali, sanjay bafna
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
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
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 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
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

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
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 Diagnostic Algorithm for Early Onset Ataxia
Rick Brandsma, Corien Verschuuren, Oebo Brouwer, Hubertus Kremer, Tom de Koning, Marina de koning-Tijssen, Deborah Sival
Tics in a child with Hashimoto encephalopathy
Padma Balaji, Vasanthi Thiruvengadam, Ashish Badaya
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

Muscle and Nerve

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
Atypical childhood-onset neuroaxonal dystrophy in an Indian girl - case report
Himani Bhasin, Sakshi Jain, Marta Romani, Enza Maria Valente, Suvasini Sharma
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
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
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
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
Factors influencing initial diagnosis of Guillain Barre syndrome : A retrospective analysis
Padma Balaji, Vasanthi Thiruvengadam

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
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
VICI SYNDROME- A RARE CASE REPORT
Giriraj Kumar Sharma, vaanathi H, padma balaji, shobana R, rahul anand yadav
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

Neurogenetics

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
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 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
Genetic profile of childhood Charcot-Marie-Tooth disease
Stuart Murray, Joshua Burns, Leah Kim, Kayla Cornett, Manoj Menezes
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
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
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
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
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
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
A study on protective effect of BDNF-MSC in Rett syndrome model
Hyo Jeong Kim, Jaesuk Lee, Delger Bayarasaikhan, Bonghee Lee
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

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
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
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

Neuroradiology

Case Report: Van der Knaap Disease
Vaishali Deshpande, Vaishali Deshpande, Sushma Save, Sandeep Bavdekar
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
Pineal cysts in children: the experience of child neurology department
sirine belghuith
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

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
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
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
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
Subacute meningitis / Prolonged fever as presentations of MOG antibody associated autoimmune demyelination syndrome – a case series
Rahul Badheka, Vrajesh Udani, Neelu Desai
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
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-radiologic spectrum and outcome of pediatric demyelinating disorders – A retrospective study
Bidisha Banerjee, Muhammed Valikandy Hafis, Ullas V Acharya
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

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
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
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

Neuro-opthalmology

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

Early Therapy in Perinatal Stroke (eTIPS): Feasibility Trial
Anna Purna Basu
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
Speech & Swallowing rehabilitation in Child with GBS: The journey from ICU to School
abhijeet vilas botre

Stroke & Neurovascular Disorders

A RARE COMPLICATION OF NEPHROTIC SYNDROME IN PEDIATRICS - ISCHEMIC STROKE
NEHA MANJHANI, SAKSHI SHARMA, RAVI SHARMA, RAJIV BANSAL, VIVEK JAIN
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
Intraarterial Embolectomy in Pediatric Arterial Ischemic Stroke
Nesibe Gevher Eroglu Ertugrul, Ceren Gunbey, Ahmet Ziya Birbilen, Ahmet Peker, Anıl Arat, Murat Arsava, Haluk Topaloglu, Dilek Yalnizoglu
Brain Magnetic Resonance imaging and angiography findings in Ugandan children with Sickle Cell Anemia; a cross sectional study
Richard Idro, Nancy Green, Deogratius Munube, Linda Buluma, Bridget Kebirungi, Robert Opoka, Paul Bangirana, Ezekiel Mupere, Edward Kayongo, Rogers Sekibira, Phillip Kasirye, Iga Matovu, Samson Kamya Lubowa, Michael Kawooya, Philip Larussa, Frank Minja
Management of Acute Stroke in Pediatric Population with Moya-Moya Disease- Our Institutional Experience
Achal Gupta, Konika Bansal, Nitin Dange
CLINICO-PATHOGENETIC CHANGES OF COMPLICATIONS OF INTRAVENTRICULAR HEMORRHAGE IN PERINATAL PERIOD AMONG CHILDREN IN UZBEKISTAN.
Makhmudjon Bakhromov


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