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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