Ye Wu

Zhixian Yang, Yuehua Zhang, Xiaoyan Liu, 2014, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophy.

Yuehua Zhang, X. Bao, H. Pan, 2005, Pediatric neurology.

Juvenile Generalized Myasthenia Gravis With AChR and MuSK Antibody Double Positivity: A Case Report With a Review of the Literature

Yuehua Zhang, X. Bao, Hongjun Hao, 2022, Frontiers in Pediatrics.

Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene

Xiaoping Yang, Zhen Shi, Yuwu Jiang, 2019, BMC Medical Genetics.

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

S. Traynelis, Hongjie Yuan, S. J. Myers, 2019, Brain : a journal of neurology.

Ming Liu, Yuwu Jiang, Ye Wu, 2018, Journal of Neurology.

Distinct magnetic resonance imaging features in a patient with novel RARS2 mutations: A case report and review of the literature.

Ye Wu, Yao Zhang, Jie Zhang, 2017, Experimental and therapeutic medicine.

Diagnosis and fine localization of deletion region in Wolf-Hirschhorn syndrome patients.

Jie Li, Yu-wu Jiang, Ye Wu, 2010, Chinese medical journal.

Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease

Xiaoping Yang, Chengfeng Zhao, Zhixian Yang, 2017, Metabolic Brain Disease.

Ten Novel Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical Cysts and a Long-Term Follow-Up Research

Yuwu Jiang, Yanling Yang, Jiangxi Xiao, 2016, PloS one.

Identification in Chinese patients with GLIALCAM mutations of megalencephalic leukoencephalopathy with subcortical cysts and brain pathological study on Glialcam knock-in mouse models

Zhen Shi, Yuwu Jiang, Yanling Yang, 2019, World Journal of Pediatrics.

A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavin

Zhen Shi, Yuwu Jiang, Kaili Shi, 2019, BMC Medical Genetics.

Fifteen Novel EIF2B1-5 Mutations Identified in Chinese Children with Leukoencephalopathy with Vanishing White Matter and a Long Term Follow-Up

Yuwu Jiang, Ye Wu, Xi-ru Wu, 2015, PloS one.

[Analysis of HEPACAM mutations in a Chinese family with megalencephalic leukoencephalopathy with subcortical cysts].

Yu-wu Jiang, Ye Wu, Xi-ru Wu, 2012, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Yuwu Jiang, Ye Wu, Xi-ru Wu, 2011, Journal of Human Genetics.

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability

Yuehua Zhang, Yuwu Jiang, Xiaoyan Liu, 2015, Epilepsia.

Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation.

Yuwu Jiang, Wenshu XiangWei, Jinliang Li, 2019, Gene.

Functional Study of TMEM163 Gene Variants Associated with Hypomyelination Leukodystrophy

M. Burmeister, T. Kubisiak, Yuwu Jiang, 2022, Cells.

Congenital muscular dystrophies in China

Zhaoxia Wang, Yun Yuan, C. Bönnemann, 2019, Clinical genetics.

Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder

Z. Xiong, Xiaoli Chen, Yuwu Jiang, 2015, BMC Pediatrics.

De novo KCNMA1 mutations in children with early‐onset paroxysmal dyskinesia and developmental delay

Yu-wu Jiang, Ye Wu, K. Gao, 2015, Movement disorders : official journal of the Movement Disorder Society.

Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers

X. Bao, Yuwu Jiang, H. Ren, 2019, Front. Neurol..

Functional Studies of MLC1 Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical Cysts

Yuwu Jiang, Ye Wu, Xi-ru Wu, 2012, PloS one.

A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood

Zhixian Yang, Yuehua Zhang, X. Bao, 2009, Brain and Development.

Functional Study of NIPA2 Mutations Identified from the Patients with Childhood Absence Epilepsy

T. Netoff, Yuehua Zhang, Yuwu Jiang, 2014, PloS one.

Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter disease

C. Proud, Xuemin Wang, Yuwu Jiang, 2011, Journal of Human Genetics.

Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease

Jie-ling Li, Yuwu Jiang, Ye Wu, 2009, Journal of Human Genetics.

Correlation Between Genotype and Age of Onset in Leukoencephalopathy With Vanishing White Matter

Yuwu Jiang, Ye Wu, Jingmin Wang, 2021, Frontiers in Genetics.

[Clinical characteristics of cases with leukoencephalopathy with vanishing white matter].

Yuehua Zhang, Yanling Yang, Jiangxi Xiao, 2007, Zhonghua er ke za zhi = Chinese journal of pediatrics.

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy

P. Chan, R. Du, Yuehua Zhang, 2012, Human Genetics.

Efficacy of Anti-seizure Medications, Quinidine, and Ketogenic Diet Therapy for KCNT1-Related Epilepsy and Genotype-Efficacy Correlation Analysis

Yuehua Zhang, Yuwu Jiang, Ying Yang, 2022, Frontiers in Neurology.

Identification of GJC2 gene mutations in chinese patients with Pelizaeus-Merzbacher-like disease.

Yuwu Jiang, Jiangxi Xiao, Ye Wu, 2016, Minerva pediatrica.

Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus–Merzbacher disease

Yuwu Jiang, Ye Wu, Xi-ru Wu, 2015, Brain and Development.

Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis.

Yuehua Zhang, Ling Zhang, A. Yu, 2018, Advances in neurobiology.

[Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression].

Yun Yuan, Yuehua Zhang, X. Bao, 2006, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Efficacy of methylprednisolone therapy for electrical status epilepticus during sleep in children].

Yuehua Zhang, X. Bao, Yuwu Jiang, 2014, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Optimal Use of Perampanel in Asian Patients with Epilepsy: Expert Opinion

Takamichi Yamamoto, Chin-Wei Huang, Jing Ding, 2021, Therapeutics and clinical risk management.

Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS)

Zhixian Yang, Yuehua Zhang, X. Bao, 2020, Orphanet Journal of Rare Diseases.

Clinical characteristics of two cohorts of infantile spasms: response to pyridoxine or topiramate monotherapy

Zhixian Yang, Yuehua Zhang, J. Xue, 2018, World Journal of Pediatrics.

Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.

Zhaoxia Wang, Yun Yuan, Y. Qi, 2007, Mitochondrion.

Postoperative seizure and developmental outcomes of children with hemimegalencephaly and drug-resistant epilepsy

Ming Li, Qingzhu Liu, Yuwu Jiang, 2021, Seizure.

CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia

X. Bao, Hong Jiang, Yuwu Jiang, 2023, Movement disorders : official journal of the Movement Disorder Society.

Natural history and genotype‐phenotype correlation of pantothenate kinase‐associated neurodegeneration

Yuwu Jiang, Ye Wu, Jingmin Wang, 2020, CNS neuroscience & therapeutics.

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations

Zhixian Yang, Yuehua Zhang, X. Bao, 2014, Brain and Development.

Remote programming: A convenient and cost-effective measure of vagus nerve stimulation for children with epilepsy

Qingzhu Liu, Yuwu Jiang, Ye Wu, 2019, Epilepsy Research.

Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II

Ming Liu, Qingzhu Liu, Yuwu Jiang, 2018, Journal of Neuroinflammation.

Follow-up study on Chinese children with relapsing MOG-IgG-associated central nervous system demyelination.

Yuehua Zhang, X. Bao, Yuwu Jiang, 2019, Multiple sclerosis and related disorders.

[Clinical characteristics and long-term prognosis of Landau-Kleffner syndrome].

Yuehua Zhang, X. Bao, Yu-wu Jiang, 2006, Zhonghua er ke za zhi = Chinese journal of pediatrics.

The effects of antiepileptic drugs on spatial learning and hippocampal protein kinase C γ in immature rats

Li Wang, Ye Wu, 2002, Brain and Development.

ARSA gene mutations in five Chinese metachromatic leukodystrophy patients.

X. Bao, Yuwu Jiang, H. Pan, 2007, Pediatric neurology.

Effects of Stable Vagus Nerve Stimulation Efficacy on Autistic Behaviors in Ten Pediatric Patients With Drug Resistant Epilepsy: An Observational Study

Luming Li, Yuwu Jiang, H. Hao, 2022, Frontiers in Pediatrics.

Pilot trial on the efficacy and safety of pantethine in children with pantothenate kinase-associated neurodegeneration: a single-arm, open-label study

Yuwu Jiang, Ye Wu, Jingmin Wang, 2020, Orphanet Journal of Rare Diseases.

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort

Liping Wei, Zhixian Yang, Yuehua Zhang, 2017, Journal of Human Genetics.

Negative myoclonus in a child with anti-NMDA receptor encephalitis

I. Fernández, L. Ren, J. Jiao, 2015, Journal of the Neurological Sciences.

Vagus nerve stimulation in children with drug-resistant epilepsy of monogenic etiology

Qingzhu Liu, Ye Wu, T. Ji, 2022, Frontiers in Neurology.

Somatic variants in new candidate genes identified in focal cortical dysplasia type II

Ming Liu, Qingzhu Liu, Yuwu Jiang, 2020, Epilepsia.

Clinical study and PLA2G6 mutation screening analysis in Chinese patients with infantile neuroaxonal dystrophy

Yun Yuan, Y. Yuan, Y. Jiang, 2009, European journal of neurology.

The recurrent mutation in RNF220 also causes hypomyelination in China and is a CpG hot spot.

M. Burmeister, T. Kubisiak, Yuwu Jiang, 2022, Brain : a journal of neurology.

Phenotypic spectrum of mutations in IBA57, a candidate gene for cavitating leukoencephalopathy

Ming Liu, M. Liu, Yuwu Jiang, 2018, Clinical genetics.

Yuwu Jiang, Ye Wu, Han Zhang, 2021, Frontiers in Pediatrics.

A Patient With CAD Deficiency Responsive to Uridine and Literature Review

Ye Wu, Tianshuang Wang, Ling Zhou, 2020, Frontiers in Neurology.

Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II

Ming Liu, Qingzhu Liu, Yuwu Jiang, 2018, Journal of Neuroinflammation.

Negative myoclonus in a child with anti-NMDA receptor encephalitis

I. Fernández, L. Ren, J. Jiao, 2015, Journal of the Neurological Sciences.

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations

Zhixian Yang, Yuehua Zhang, X. Bao, 2014, Brain and Development.

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability

Yuehua Zhang, Yuwu Jiang, Xiaoyan Liu, 2015, Epilepsia.

[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy].

Zhixian Yang, Yuehua Zhang, Xiaoyan Liu, 2014, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Characterization of developing rat cortical neurons after epileptiform discharges

Yuwu Jiang, Ye Wu, Xi-ru Wu, 2010, International Journal of Developmental Neuroscience.

[Clinical and electrophysiologic studies on epileptic negative myoclonus in atypical benign partial epilepsy of childhood].

Zhixian Yang, Yuehua Zhang, X. Bao, 2008, Zhonghua er ke za zhi = Chinese journal of pediatrics.