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 |
| 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 |
| Efficacy of Botulinum Toxin on Spasticity and Functional Outcome in Cerebral Palsy: an evaluation | |
| Lokesh Lingappa |
| 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 |
CNS Infections
| Good Hearing Outcome in Children with non-polio Enteroviral Meningitis | |
| Chew Thye Choong, Elis Lee, Henry Tan, Natalie Tan |
| YIELD OF GENEXPERT AND OUTCOMES IN PEDIATRIC TUBERCULAR MENINGITIS | |
| Lokesh Lingappa |
Development Cognition and Psychiatry
| 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 |
| 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 Effect of Glucocorticoid Receptor (GR) Function on the Behavior of ADHD Rats and the Mechanism of Interaction between GR and MAO A | |
| Yanhui Chen, Hongzhu Lu, Jun Hu, Xiaoxia Lin |
| Plasma amino acid profile in children with autism spectrum disorder | |
| Wen-Xiong Chen, Min-Zhi PENG, Yan-Na CAI, Zhi-Fang HUANG, Jin-Yu HUANG, Si-Yuan YANG, Peng YI, Li LIU |
| Acupuncture for non-verbal autistic children: a randomized controlled trial | |
| Wen-Xiong Chen, Gang LIU, Hong-Sheng LIU, Zhi-Fang HUANG, Jin-Yu HUANG, Si-Yuan YANG |
| Early Detection of Developmental Problems by Parents | |
| Sundara sabaratnam Sam LINGAM |
| Diagnostic Investigations of Children with Learning Difficulties | |
| Sundara sabaratnam Sam LINGAM |
| Autism and ADHD: Differential functioning on a Computerized Performance Test (MOXO-CPT) | |
| YAEL LEITNER |
Epilepsy
| Classifying Electroencephalographic Diagnoses of Epilepsy without Epileptiform Discharges and Nonepileptic Paroxysmal Events Using Deep Convolutional Neural Networks | |
| Lung-Chang Lin, Chen-Sen Ouyang, Ching-Tai Chiang, Rong-Ching Wu, Hui-Chuan Wu, Rei-Cheng Yang |
| Factors associated with Electroencephalographic and Clinical Remission of Benign Childhood Epilepsy with Centrotemporal Spikes | |
| Su Jeong You, Eun Hye Lee |
| Perampanel and Brivaracetam: Efficacy and safety in pediatric refractory epilepsy | |
| Divya Subramanian Khurana, Ana Melikishvili, Sara McGuire, Karen S Carvalho, Ignacio Valencia, Daphne M Hasbani, Uzma Sharif, Agustin Legido |
| A critical analysis of lumbar puncture in the emergency management of febrile seizures: a cross-sectional study | |
| Eduardo Jorge da Fonseca Lima, Gabriel Brito de Moura Monteiro, Alberto de Barros Lima Filho, Lucas Victor Alves |
| The absence of NIPA2 enhances neural excitability through BK channels | |
| Han Xie, Nana Liu, Wenshu Xiangwei, Kai Gao, Tianshuang Wang, Yuwu Jiang |
| The efficacy and safety of levetiracetam treating in pediatric epilepsy in different ages and seizure types | |
| Yu Liu, Xueying Wang, Gaobo Ye, Shaoping Huang, Lin Yang |
| 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 |
| Clinical and EEG characteristics of epilepsy of infancy with migrating focal seizures | |
| Shuqian Zhang, Ruopeng Sun, Baomin Li |
| De novo Mutation among a Chinese Infantile Spasms Cohort and Precision Treatment with Levetiracetam in Four de novo STXBP1 Mutation Patients | |
| Li-ying Liu, Fang Liu, Yang-yang Wang, Gui-Xia Zhang, Meng-Na Zhang, Qian Lu, Li-Ping Zou, Xiao-Li Chen |
| The value of mobile phone videos in increasing the diagnosis accuracy and saving cost of consultation for infant paroxysmal events: a prospective study in China | |
| Lu-Lu Huang, Yang-Yang Wang, Li-Ying Liu, Hong-Ping Tang, Meng-Na Zhang, Shu-Fang Ma, Li-Ping Zou |
| Establishment and utility assessment of Posterior Reversible Encephalopathy Syndrome early warning scoring (PEWS) scale Establishment and utility assessment of PEWS scale | |
| Li-Ping Zou, Hui Li, Li-ying Liu, Yang-yang Wang, Ying Liu, Jing Chen, Lin-Yan Hu, Meng-Jia Liu, Meng-Na Zhang, Shu-Fang Ma |
| Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation | |
| ChunHong Chen, HuSheng Wu, XiaoHui Wang, HongMei Wang, XiaoTun Ren, JunLan Lv, Fang Fang |
| Effectiveness and tolerability of perampanel in children under 7 years old with refractory epilepsy: A single-center, retrospective study | |
| Fu-Man Chang, Wen-Chin Weng, Pi-Chuan Fan, Wang-Tso Lee |
| What to expect from an unexpected seizure? | |
| Rosa Lualdi, Giulia Bravar, Valentina Dolcemascolo, Paola Cogo, Giovanni Crichiutti |
| Clinico-radiological and electrographic spectrum of children with Temporal lobe epilepsy: a retrospective cohort study | |
| Zulfiqar Luhar, Biswaroop Chakrabarty, Ankita Pal, Prashant Jauhari, Atin Kumar, Shobha Sharma, Sheffali Gulati |
| Microbiological diagnostic challenges in a seasonal cluster of Rhombencephalitis | |
| smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Milind Shah, Srikanth Domala, Ashwini Mohan, Ravi verma |
| Prolonged Seizures in Children | |
| Clodagh Mitchell, Jay Shetty, Libby Dickson, Celia Brand, Paul Leonard, Ailsa McLellan |
| Significance of polyspikes on electroencephalogram in children with focal epilepsy | |
| Ara Ko, Ju Hyun Kong, Yun-Jin Lee, Sang Ook Nam |
| Genotype and phenotype of epileptic patients with SCN2A mutations | |
| Qi Zeng, Xiaoling Yang, Dan Wang, Jing Zhang, Jiaoyang Chen, Aijie Liu, Xiaoyan Liu, Xiru Wu, Yuwu Jiang, Yuehua Zhang |
| The electroclinical features of CHD2 mutation related epilepsy | |
| Jiaoyang Chen, Jing Zhang, Qi Zeng, Liping Zhang, Hua Li, Zhixian Yang, Xiaoling Yang, Aijie Liu, Yuehua Zhang |
| Clinical characteristics and epilepsy outcomes after surgery in children with focal cortical dysplasia type II | |
| tianshuang wang, Ming Liu, Jie Zhang, Lixin Cai, Qingzhu Liu, Yuwu Jiang, Ye Wu |
| Semiological, Diagnostic and theraupetic challenges in Infantile onset epilepsy | |
| Smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Shah, Srikanth Domala, Prasanthi Aripirala, Ravi verma |
| Simultaneous quantification of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate, pipecolic acid and alpha-aminoadipic acid in pyridoxine-dependent epilepsy | |
| Zhixian Yang, Jiao Xue, Pan Gong, Junjuan Wang, Minhang Wu, Wenshuang Yang, Shiju Jiang, Ye Wu, Yuwu Jiang, Yuehua Zhang, Tatiana Yuzyuk, Hong Li |
| Outcome Following Febrile Seizures: A Scottish Population Cohort | |
| Libby CHATTERTON DICKSON, Ailsa McLellan, Paul Leonard, Clodagh Mitchell, Jay Shetty |
| Experience with Isoflurane in Paediatric Super Refractory Status Epilepticus | |
| Ashwini Mohan, Lokesh Lingappa, Ramesh Konanki, Nikit Shah, Smilu Mohanlal, Farhan Shaikh, anupama Y, shashwat Mohanty |
| Clinical spectrum and therapeutic outcomes of electrical status epilepticus during sleep in children | |
| Bing-Wei PENG, Hai-Xia Zhu, Xiu-Ying WANG, Xiao-Jing LI, Hui-Ci LIANG, Feng-Qiong ZHANG, SHu-Yao Ning, Yan-Ying Zhong, Wen-Xiong Chen |
| Febrile Infection Related Epilepsy Syndrome (FIRES) – A rare cause of super refractory status epilepticus | |
| Aanchal Pradeep Khemani, Sanjay Bafna, Sagar Lad, Nandan Yardi |
| Neonatal-onset epilepsy: Clinico-etiological spectrum and short-term outcome | |
| Prasanthi Aripirala, Ramesh Konanki, Lokesh Lingappa |
Headache
| Relapsing factors for pediatric migraine | |
| KON-HEE LEE |
Metabolic Disorders
| Leigh-like syndrome due to homoplasmic m.8993T>G variant with hypocitrullinemia and unusual biochemical features suggestive of multiple carboxylase deficiency (MCD) | |
| Maina Padmanabha Kava, Barry Lewis, Lawrence Greed, Shanti Balasubramaniam |
| Large-single scale mitochondrial DNA deletions in different tissues of patients with Kearns-Sayre syndrome | |
| yuqing shi, fang fang, zhimei liu |
| Fatal neonatal lactic acidosis secondary to a novel defect in COX16 causing complex IV deficiency | |
| Maina Padmanabha Kava, Shanti Balasubramaniam, Barry Lewis, Richard Rodenburg |
| TRPM6 gene mutation resulted in primary hypomagnesemia with secondary hypocalcemia（HSH） in 3 cases | |
| xiaohui wang, shen zhang, weihua zhang, jiuwei li, changhong ding, fang fang |
| Lysine- restricted diet in a child with pyridoxine -dependant epilepsy prevents long term developmental delay | |
| Leah Queit, Maina Padmanabha Kava, Barry Lewis, Lawrence Greed, Peter Williams Rowe, Shanti Balasubramaniam |
| Treatable Leigh syndrome involving mitochondrial cofactor metabolism | |
| Zhimei Liu, Fang Fang |
| Infantile-onset mitochondrial disorder associated with COQ4 missense mutations | |
| Leechin Wong, WangTso Lee |
| Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET) imaging and motor and sensory neurophysiology in children with Glutaric Aciduria(GA1) dystonia awaiting Deep Brain Stimulation Surgery (DBS) | |
| Stavros Tsagkaris, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Verity McClelland, Alexander Hammers, Jean-Pierre Lin |
| Clinical and genetic analysis of progressive cavitating leukoencephalopathy in China | |
| Ren Changhong, Fang Fang, Zhimei Liu |
Movement Disorders
| Rett syndrome in Taiwan: genotype and phenotype characteristics | |
| Leechin Wong, WangTso Lee |
| 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 |
| 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
| Impact of genetic results on treatment of CONGENITAL MYASTHENIC SYNDROME (CMS) | |
| RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, BINDU MADHAVI PARICHURI, SMILU MOHANLAL |
| Genetic evaluation of Congenital Myopathy (CM) and Congenital Muscular Dystrophy (CMD) in children : Slow Death of Muscle biopsies | |
| RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, PRASHANTHI ARIPRALA, RAMPRASAD VL, THENRAL SG |
| Anti –HMG-Co A reductase antibodies associated with progressive necrotizing myositis and autophagosomes in a teenager | |
| Eleanor Ng, Maina Padmanabha Kava, Peter Williams Rowe, Simon Williams, Phillipa Lamont, Rei Curd Junckerstorff |
| Clinical and genetic characteristics of congenital myasthenia syndrome with episodic apnea caused by CHAT gene mutation in China | |
| Zhimei Liu, Fang Fang |
| A Case of Congenital Myasthenia with False Positive Anti-acetylcholine Receptor antibody | |
| Chee Geap Tay, Limin Li, Chin Seng Gan, Chee Ming Teh, Vigneswari Ganesan, Choong Yi Fong |
| Clinical and genetic characteristics of GDAP1 gene mutation in Charcot Marie Tooth disease | |
| JUN LAN LU, JUN LAN LU |
| 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 |
Neonatal and Fetal Neurology
| Late MR Spectroscopy is not Recommended in the Evaluation of Neonatal Hypoxic Ischemic Encephalopathy (HIE). | |
| Suhasini Kauskal, Christabel Lee, Paola Pergami |
Neurogenetics
| Clinical and hereditary characteristics of MECP2 duplication syndrome in Chinese patients | |
| zhanwen he, Xiangyang Luo, Liyang Liang |
| Cerebral infarction, growth retardation and severe intellectual disability in Korean patients with de novo duplication of 14q32.2 | |
| Ji Yoon Han, In Goo Lee |
| Two 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 |
| Next Generation Sequencing Based Multi-gene Testing of Over 1000 Indian Patients Affected with Neurological Disorders Revealed an Improved (>40%) Diagnostic Yield | |
| Ashraf U Mannan, Aparna Ganapathy, Avshesh Mishra, Anil Vittal Kanthi, Megha Rani Soni, Irene Patric, Aparajit Sridharan, Sobha George, Lakshmi Mohan, Swathi M Chinnappa, Ankitha Prabhudev, Syama Sreedharan, Thyagarajan Chandrasekaran, Priyanka K, Mukunth Sadagopan, Aswathy S L, Vidya H K, Satish Sankaran, Shanmukh Katragadda, Vamsi Veeramachaneni, Ramesh Hariharan, Vijay Chandru |
| 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 |
| Genotype and phenotype analysis of Leigh syndrome involving valine metabolism in 8 Chinese children | |
| Xiaodi Han, Fang Fang, Zhimei Liu |
| ATP1A3 mosaicism in families with alternating hemiplegia of childhood | |
| Xiaoling Yang, Xiaoxu Yang, Shupin Li, Qi Zeng, Jing Zhang, August Yue Huang, Adam Yongxin Ye, Zhe Yu, Sheng Wang, Yuwu Jiang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang |
| Study of the rare causative genes and analysis of genotype-phenotype correlations of Dravet syndrome | |
| Xiaojuan Tian, Qi Zeng, Jing Zhang, Aijie Liu, Xiaoling Yang, Yuwu Jiang, Xiru Wu, Yuehua Zhang |
| The Study of Genotype-phenotype Correlation in Patients with Alternating Hemiplegia of Childhood | |
| Shupin Li,, Xiaoling Yang, Jiaoyang Chen, Qi Zeng, Jing Zhang, Yuehua Zhang |
| The mosaicism and incomplete penetrance of PCDH19 mutations | |
| Aijie Liu, Xiaoxu Yang, Xiaoling Yang, Qixi Wu, Jing Zhang, Dan Sun, Zhixian Yang, Yuwu Jiang, Xiru Wu, Liping Wei, Yuehua Zhang |
| 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 |
| Modeling vanishing white matter disease with patient-derived induced pluripotent stem cell reveals astrocytic dysfunction | |
| Ling Zhou, Peng Li, Na Chen, Lifang Dai, Yinan Liu, Li Shen, Jingmin Wang, Yuwu Jiang, Ye Wu |
| AicardiGoutieres - A close mimick of congenital infection: Case series with 3 children and 4 families | |
| Beena Suresh, Sujatha Jagadeesh, Vaishnavi Reddy, Min Lee-Kirsch |
| Natural history and genotypic spectrum of cavitating leukoencephalopathy in childhood | |
| Jie zhang, Ming Liu, Zhongbin Zhang, Ling Zhou, Weijing Kong, Yuwu Jiang, Jingmin Wang, Jiangxi Xiao, Ye Wu |
| A study on protective effect of BDNF-MSC in Rett syndrome model | |
| Hyo Jeong Kim, Jaesuk Lee, Delger Bayarasaikhan, Bonghee Lee |
| “STUDY OF CLINICO-ETIOLOGICAL PROFILE OF EARLY ONSET EPILEPTIC ENCEPHALOPATHY IN CHILDREN’’ | |
| Boda Praful Kumar, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, RADHA RAMA DEVI, PRASHANTHI ARIPIRALA, THENRAL SG |
| Whole Exome Sequencing in Diagnose of Patients with Leukodystrophy | |
| Hsin Pei Wang, Wang-Tso Lee |
| 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 |
| Diversity of phenotypes in Infantile Seizure and their families with PRRT2 Mutations | |
| TUNG MING CHANG, Inn Chi Lee, Ming Chen, Yuh Jyh Jong |
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 |
| Brain Death Determination for Comatose Patients in The Pediatric Intensive Care Unit | |
| Kun-Long Hung, Su-Ching Hu, Wong Lee-Chin |
Neuroradiology
| Intracerebral large artery disease with Aicardi-Goutières Syndrome | |
| Chung Jane Ng, Wang Tso Lee |
| Brain MRI in children with Wilson Disease | |
| yuan wu, Ying Zhu, Ting Zhang, Ming Li |
Neuroimmunology
| MicroRNA-181a-5p regulates blood brain barrier permeability after meningoencephalitis via positive regulating HMGB1 expression | |
| Ling-juan Liu |
| Clinical and prognostic analysis of ocular myasthenia gravis in children | |
| Chen Jiji, Jiang Li, Li Xiujuan, Hong Siqi |
| 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 |
| 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 |
| Use of the radiotracer 18F-GE180 for PET scan imaging of active neuro-inflammation in children with multiple sclerosis | |
| Badal G Jain, Hua Li, Zhang Shaohui, Xuyi Yue, Rahul Nikam, Alana Salvucci, Yangchun Xin, Diane Chugani, Harry Chugani |
| Familial acute necrotizing encephalopathy (ANE1) | |
| Zoltan Liptai, Sarolta Dobner, Peter Benke, Anna Szocs, Judit Moser, Fleur Vansenne |
Neurosurgery
| Functional mapping of the brain by novel tripolar EEG electrodes | |
| Sameer C Dhamne, Damon Hyde, Shunan Li, Walt Besio, Alexander Rotenberg |
Neurooncology
| A randomized, double-blind, parallel group, placebo-controlled trial of metformin in tuberous sclerosis complex | |
| Sam Amin, Andrew A Mallick, Hannah Edwards, Andrew Lux, Amjad Khan, Matthew Laugharne, Marcus Likeman, Finbar O'Callaghan |
Neuro-opthalmology
| Cerebral vision impairment in children: How much of it is preventable? | |
| Ramesh Konanki, Sravanthi Kuruva, Lokesh Lingappa, Nikit Milind Shah, Srikanth Domala |
Neuroendocrinology
| Effect of Glucocorticoid Receptor’s Function on Expression of MAOA by GC-KLF11-MAOA Pathway | |
| Yanhui Chen, Jie Zheng, Xiaoxia Lin, Jun Hu |
Stroke & Neurovascular Disorders
| Comorbidity of Myhre syndrome and Moyamoya disease: a case report and literature review | |
| qun li Liu, juan ling Liu, an ding Mao |
| RNF213 mutation in child with DMD carrier combined with Moyamoya disease | |
| Ji Yoon Han, Yun Tae Lee |
| Validation of Cerebrovascular Reactivity Imaging in Children | |
| Kenda Alhadid, Jackie Leung, William Logan, Nomazulu Dlamini |
| Pediatric ischemic stroke associated to deficiency of adenosine deaminase 2 (DADA2). | |
| José Albino da Paz, Tayrine Gonçalves, César Alves, Leandro Lucato |
| Utility of Testing for Prothrombotic Disorders in Children with Perinatal Periventricular Venous Infarction | |
| Noa Mandel-Shorer, Daune MacGregor, Suzanne Laughlin, Leonardo Brandao, Gabrielle deVeber, Nomazulu Dlamini, mahendranath moharir |
| Blood Oxygen Level Dependent (BOLD) MRI Cerebrovascular Reactivity as a Predictor of Ischemic Risk in Children with Moyamoya | |
| Nomazulu Dlamini, Mahmoud Slim, Fenella Kirkham, Manohar Shroff, Peter Dirks, Mahendranath Moharir, Daune MacGregor, Amanda Robertson, Gabrielle deVeber, William Logan |
| 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 |
| Surgical Challenges in Management of Moya Moya Syndrome- A illustrative Case series | |
| Lokesh Lingappa |
| Recurrent Strokes in Mineralizing Angiopathy and Basal Ganglia Stroke | |
| Lokesh Lingappa, siddarth shah, Ramesh Konanki |
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