Presentations and Authors


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Cerebral Palsy and Neurodisability

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
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
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
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
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

CNS Infections

Changing face of Pediatric Neurotuberculosis.
Kritika Tiwari, Purva Keni Karnavat, Anaita Udwadia Hegde
Good Hearing Outcome in Children with non-polio Enteroviral Meningitis
Chew Thye Choong, Elis Lee, Henry Tan, Natalie Tan
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
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

Education and Training

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

Development Cognition and Psychiatry

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 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, Abhinav Neela, Arpita Thakker
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
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
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
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
Rare diseases presenting with Autism Spectrum Disorder (ASD); An etiological conundrum
Vrushabh Sopan Gavali, Leena Srivastava, Nirali Thakker, Sujit Jagtap

Epilepsy

KETOGENIC DIET: DO WE NEED 4:1 RATIO FOR KETOSIS?
Purva Keni Karnavat, Anaita Udwadia Hegde, Shilpa Kulkarni, Roshan Kore, Bhakti Tulaskar, Suvarna Sawant
It’s not all about seizures: Experience of Dravet Syndrome management in a Scottish Children’s Hospital
Sylvia Yuk San Tran, Elma Stephen
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
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
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
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
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 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
Clinical utility of next generation sequencing in Early-Onset Epileptic Encephalopathies
Vishal Sondhi, K M Adhikari, Vishal Vishnu Tewari, K Venkatnarayan, Rakesh Gupta
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
Effects rehabilitation with interactive metronome training on speech disorders and epilepsy patients.
Tatiana Tomenko
Our experience with use of new 2017 ILAE classification in children with epilepsy
Abhinav Sahu, Neeta Naik, AMI SHAH, Abhinav Tiwari
Utility of short term video EEG recording in diagnosis of paroxysmal events in children
abhinav ashok tiwari, neeta naik, ami shah, abhinav sahu

Headache

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

Metabolic Disorders

Expanding the phenotype of TRNT1 mutations to include Leigh syndrome.
Carolina Gorodetsky, Chantal F. Morel, Ingrid Tein
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
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
An unusual presentation of Menkes disease masquerading as a leukodystrophy with macrocephaly
Aswini Annadurai, Anshula Tayal, 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
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

Movement Disorders

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
Anti-NMDAR Encephalitis in Children ; a Malaysian Experience
Balakrishnan Priyalatha, Tajudin Tajul Arifin, Vigneswari G
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
CHILDHOOD ONSET CHRONIC ATAXIA: A CLINICAL, ETIOPATHOLOGICAL, RADIOLOGIC AND GENETIC AUDIT.
Pallavi Shriram Todase, shilpa kulkarni, sonam kothari, anaita hegde, krishankumar shah
A novel mutation in KMT2B gene causing childhood-onset generalized dystonia
Tanmayee Subhash Thombare
Early Onset Ataxia and Comorbid Dystonia: Are There Shared Biological Pathways?
Deborah Anita Sival, Marina Tijssen, Dineke Verbeek
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

Spinal Muscular Atrophy – Lower Extremity Dominant Type 2 (SMALED2)
Erdem Simsek, Sanem Yilmaz, Hepsen Mine SERIN, Seda Kanmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben
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
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
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
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
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
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
Somatosensory Evoked Potential: a normative study in children
DILIP THAKUR
Factors influencing initial diagnosis of Guillain Barre syndrome : A retrospective analysis
Padma Balaji, Vasanthi Thiruvengadam
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

Neurogenetics

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
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
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
Clinical and Genetic Correlation in Childhood Onset Pharmacoresistant Epilepsy
Ami Shah, Neeta Naik, Abhinav Sahu, Abhinav Tiwari Tiwari
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
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
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
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
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

Neurocritical care, Neurotrauma, Neuroprotection

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
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

Neuroimmunology

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
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
OPSOCLONUS-MYOCLONUS SYNDROME: SIMULTANEOUS COMBINATION IMMUNOSUPPRESSIVE THERAPY WITH EXCELLENT OUTCOME
Shailesh Barot, Anaita Hegde, Krupa Torne, Manohar Patil, Vaibhavi Barot
Spinal cord disease following Falls and minor Sporting injury: Myelitis or SCIWORA?
Terrence Thomas
Inflammatory neuropathology of infantile Alexander disease: A case report
Kengo Kora, Takeo Kato, Minako Ide, Takayuki Tanaka, Tomokatsu Yoshida
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
Brain stem encephalitis in children
Kavita P Thakkar, Yoshimi Sogawa, Amy C Goldstein, Giulio Zuccoli
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
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

Neurosurgery

Dermoid cyst mimicking Gastro esophageal reflux disease
Surabhi Kaul, Stephen Katzen, Andrew Minzenmayer, Andrew Fang, Nivedita Thakur, Manish N Shah, Rajan P Patel

Neurorehabilitation

Factors affecting adherence to a home program: a survey presenting to a tertiary care unit.
Franzina Coutinho, Akansha Shah, Shantanu Tilak, Neelu Desai

Stroke & Neurovascular Disorders

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
LONG-TERM FUNCTIONAL AND COGNITIVE OUTCOMES AFTER PEDIATRIC STROKE
Shaanvar Sh Shamansurov, Sadokat O Nazarova, Parviza T Usmanova, Nodirakhon M Tulyaganova
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
Syndromic associations in a cohort of children with moyamoya phenomenon
Atif I A Shaikh, Karthik Muthusamy, Sangeetha Yoganathan, Maya Mary Thomas, Sanjith Aaron
Prevalence of sleep-related breathing disorders in childhood stroke: A comparative study
Sandra Toutounji, Indra Narang, Mahmoud Slim, Shelly Weiss, Ann-Marie Pontigon, Jaspal Singh, Kathleen Andres, Daune MacGregor, Gabrielle deVeber, Mahendranath Moharir, Nomazulu Dlamini
Longitudinal follow up and outcome of children with moyamoya disease
khian aun tan


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