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 |
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 | |
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Our experience in the management of diffuse axonal injury patients in pediatric population and the review of literature- an institutional study. | |
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Native medicine use and lead poisoning in children | |
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Vaishali Deshpande, Vaishali Deshpande, Sushma Save, Sandeep Bavdekar |
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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 |
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OPSOCLONUS-MYOCLONUS SYNDROME: SIMULTANEOUS COMBINATION IMMUNOSUPPRESSIVE THERAPY WITH EXCELLENT OUTCOME | |
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Improved performance of the 2017 McDonald criteria for diagnosis of multiple sclerosis in children irrespective of age | |
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