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
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
To address the issue comprehensively by measuring various neurobiological parameters exclusively in children and adolescents and an effort to bridge the gap between childhood and adult aggressive behavior.
P K Maheshwari, Sagar Lavania, Vishwas K
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
Reanalysis of the whole exome sequencing raw data and the clinical information can yield additional diagnosis missed by previously commercial genetic test report in children with epilepsy and intellectual disability
Jinliang Li, Kai Gao, Yuwu Jiang
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
International Infant Hydrocephalus Study (IIHS): 5 year health outcome results of a prospective, multicentre comparison of endoscopic third ventriculostomy (ETV) and shunt for infant hydrocephalus
YAEL LEITNER

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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