Xi-ru Wu

发表

ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients

Liping Wei, Yuehua Zhang, Jie Zhang, 2014, PloS one.

Two novel gap junction protein alpha 12 gene mutations in two Chinese patients with Pelizaeus–Merzbacher-like disease

Yuwu Jiang, Xi-ru Wu, Jingmin Wang, 2010, Brain and Development.

[T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy].

Yan Shen, Yuehua Zhang, Yucai Chen, 2005, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Research on genes susceptible to childhood absence epilepsy].

Yuehua Zhang, Xi-ru Wu, Jian-min Liang, 2006, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus

Y. Qi, Yuehua Zhang, Xiaoyan Liu, 2008, Journal of Human Genetics.

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

Yun Yuan, C. Bönnemann, Chunde Li, 2021, Orphanet Journal of Rare Diseases.

Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies

Su-xia Wang, C. Bönnemann, Hai-po Yang, 2020, Biochemical Genetics.

Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients

Su-xia Wang, Zhaoxia Wang, Yun Yuan, 2020, Journal of Medical Genetics.

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.

GRIN2A mutations in epilepsy-aphasia spectrum disorders

Zhixian Yang, Yuehua Zhang, P. Qian, 2017, Brain and Development.

OP0216 The Functional Rather than Nonfunctional LILRA3 Contributes to Susceptibility and Subphenotypes of Systemic Lupus Erythematosus and SjÖGren's Syndrome

X. Zuo, Xuejun Zhang, Yong Cui, 2014 .

Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation

Yuwu Jiang, Yanling Yang, N. Zhong, 2010, BMC Medical Genetics.

Zhixian Yang, Yuehua Zhang, Liping Zhang, 2020, Developmental medicine and child neurology.

De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsy

Yuehua Zhang, Yuwu Jiang, Yujia Zhang, 2019, Epilepsy Research.

Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations

Zhixian Yang, Yuehua Zhang, Liping Zhang, 2019, Seizure.

Genotype/phenotype of 6 Chinese cases with Niemann-Pick disease type C.

K. Higaki, E. Nanba, Yuehua Zhang, 2012, Gene.

Niemann-Pick disease type C: analysis of 7 patients

Yuehua Zhang, X. Bao, Xi-ru Wu, 2012, World Journal of Pediatrics.

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

Zhixian Yang, Yuehua Zhang, Xiaoyan Liu, 2013, BMC Neurology.

Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.

Yan Shen, Yuehua Zhang, X. Bao, 2004, Chinese medical journal.

Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome

Yuehua Zhang, X. Bao, Qingping Zhang, 2019, Seizure.

Mosaicism and incomplete penetrance of PCDH19 mutations

Liping Wei, Jing Zhang, Zhixian Yang, 2018, Journal of Medical Genetics.

Alterations of NR2B and PSD-95 expression after early-life epileptiform discharges in developing neurons

Yuwu Jiang, Xi-ru Wu, Jingmin Wang, 2007, International Journal of Developmental Neuroscience.

Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients

Liping Wei, X. Bao, Jie Zhang, 2014, BMC Medical Genetics.

A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients

T. Toda, X. Bao, Hai-po Yang, 2019, Clinical genetics.

Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation

T. Toda, T. Endo, Yuwu Jiang, 2016, Journal of Human Genetics.

Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

Yun Yuan, C. Bonnemann, Hai-po Yang, 2014, PloS one.

Allelic variations of glut-1 deficiency syndrome: the chinese experience.

Hong Yang, K. Engelstad, Dong Wang, 2012, Pediatric neurology.

A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy

S. Sugano, Yutaka Suzuki, Y. Hayashi, 2015, Human Genome Variation.

Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene

X. Bao, Qingping Zhang, Yan Chen, 2019, Molecular genetics & genomic medicine.

Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients

T. Toda, Hai-po Yang, Jiangxi Xiao, 2015, Brain and Development.

Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients

T. Toda, T. Endo, Yanling Yang, 2013, Molecular Genetics and Genomics.

Fukutin gene retrotransposal insertion in a non‐Japanese Fukuyama congenital muscular dystrophy (FCMD) patient

Yun Yuan, T. Toda, Yuwu Jiang, 2009, American journal of medical genetics. Part A.

The Efficacy of Ketogenic Diet in 60 Chinese Patients With Dravet Syndrome

Yuehua Zhang, Xiaoling Yang, Ye Wu, 2019, Front. Neurol..

Novel SLC16A2 mutations in Chinese patients with Allan-Herndon-Dudley Syndrome

X. Bao, Qingping Zhang, Jiaping Wang, 2018, Translational Science of Rare Diseases.

Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy

Zhixian Yang, Huixia Yang, Yuehua Zhang, 2018, International journal of genomics.

Familial cases and male cases with MECP2 mutations

Liping Wei, X. Bao, Jiarui Li, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[Association of genetic polymorphisms in methionine metabolism genes with X-linked adrenoleukodystrophy].

X. Bao, Ye Wu, Xi-ru Wu, 2011, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Prenatal diagnosis of X-linked adrenoleukodystrophy].

Yuehua Zhang, X. Bao, H. Pan, 2007, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

MECP2 mutation spectrum and its clinical characteristics in a Chinese cohort

X. Bao, Qingping Zhang, Y. Wen, 2020, Clinical genetics.

Clinical and genetic study in Chinese patients with Alexander disease.

Yuwu Jiang, Yanling Yang, Ye Wu, 2008 .

Acute metabolic crisis induced by vaccination in seven Chinese patients.

Yuehua Zhang, Yuwu Jiang, Yanling Yang, 2006, Pediatric neurology.

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.

Zhaoxia Wang, Yun Yuan, Y. Qi, 2006, Chinese medical journal.

Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients

T. Toda, T. Endo, Yanling Yang, 2013, Molecular Genetics and Genomics.

Alpers syndrome with prominent white matter changes

Yun Yuan, Yuehua Zhang, L. Wong, 2008, Brain and Development.

Neuropathologic and Clinical Features in Eight Chinese Patients With Leigh Disease

Yu-wu Jiang, Xi-ru Wu, Jiong Qin, 2002, Journal of child neurology.

Analysis of the Parental Origin of De Novo MECP2 Mutations and X Chromosome Inactivation in 24 Sporadic Patients With Rett Syndrome in China

X. Bao, H. Pan, Xi-ru Wu, 2010, Journal of child neurology.

Long-term effects of seizures in neonatal rats on spatial learning ability and N-methyl-D-aspartate receptor expression in the brain.

Yuwu Jiang, Xi-ru Wu, Jingmin Wang, 2004, Brain research. Developmental brain research.

Characterization of developing rat cortical neurons after epileptiform discharges

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

Early-life epileptiform discharges exert both rapid and long-lasting effects on AMPAR subunit composition and distribution in developing neurons

Yuwu Jiang, Ye Wu, Xi-ru Wu, 2008, Neuroscience Letters.

Association between genetic variation of CACNA1H and childhood absence epilepsy

Zhijian Yao, Yan Shen, P. Chan, 2003, Annals of neurology.

Spinal Cord Demyelination Associated with Biotinidase Deficiency in 3 Chinese Patients

Yuehua Zhang, Y. Hasegawa, S. Yamaguchi, 2007, Journal of child neurology.

Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients

Zhixian Yang, Yuehua Zhang, X. Bao, 2018, PloS one.

Outcome of organic acidurias in China.

Y. Hasegawa, S. Yamaguchi, Yuwu Jiang, 2008, Annals of the Academy of Medicine, Singapore.

[Diagnosis and treatment of biotinidase deficiency-clinical study of six patients].

Yuehua Zhang, X. Bao, Y. Hasegawa, 2003, Zhonghua er ke za zhi = Chinese journal of pediatrics.

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

Liping Wei, X. Bao, Jiarui Li, 2017, BMC Medical Genetics.

Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy

Y. Qi, Yuehua Zhang, Xiaoyan Liu, 2008, Epilepsia.

FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies

Hai-po Yang, Yanling Yang, Xi-ru Wu, 2016, Journal of Human Genetics.

ATP1A3 mosaicism in families with alternating hemiplegia of childhood

A. Y. Ye, Liping Wei, Zhe Yu, 2019, Clinical genetics.

Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome

A. Y. Ye, Meng Wang, Liping Wei, 2015, Human mutation.

X Chromosome Inactivation in Rett Syndrome and Its Correlations With MeCP2 Mutations and Phenotype

Xi-ru Wu, Xinhua Bao, Shengling Jiang, 2008, Journal of child neurology.

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

R. Du, Ling Zhang, Yuwu Jiang, 2018, Scientific Reports.

Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage‐sensitive genes with clinical severity in genomic disorders

J. Lupski, C. Carvalho, Hongyan Wang, 2017, Human molecular genetics.

High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability

Yiping Shen, Bai-Lin Wu, Y. An, 2012, PloS one.

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities

Yuehua Zhang, Yuwu Jiang, Xiaoyan Liu, 2015, PloS one.

Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

X. Bao, Qingping Zhang, Y. Wen, 2018, BMC medical genetics.

RNAi-induced down-regulation of Mecp2 expression in the rat brain

X. Bao, H. Pan, Xi-ru Wu, 2008, International Journal of Developmental Neuroscience.

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

A. Y. Ye, Liping Wei, Zhe Yu, 2017, Scientific Reports.

[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].

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

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome

Zhixian Yang, Y. Qi, Yuehua Zhang, 2010, Journal of Human Genetics.

Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Liping Wei, Qixi Wu, X. Bao, 2018, Genetics in Medicine.

Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals

Meng Wang, Liping Wei, Linlin Yan, 2014, Cell Research.

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

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

Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing

Hai-po Yang, Yanling Yang, Xiaoqing Li, 2017, Scientific Reports.

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy

Dan-hua Zhao, Yun Yuan, C. Bonnemann, 2014, World Journal of Pediatrics.

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.

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.

Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation

Liping Wei, X. Bao, Jiarui Li, 2017, BMC Medical Genetics.

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.

Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Liping Wei, Xiaoxu Yang, Qixi Wu, 2018, Genetics in Medicine.

Molecular characteristics of Chinese patients with Rett syndrome.

Liping Wei, X. Bao, Jie Zhang, 2012, European journal of medical genetics.

MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome

X. Bao, H. Pan, Xi-ru Wu, 2006, Journal of Human Genetics.

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

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

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.

[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.

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.

Childhood absence epilepsy: Elctroclinical features and diagnostic criteria

Zhixian Yang, Yuehua Zhang, Xiaoyan Liu, 2011, Brain and Development.

[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.

[A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].

Q. Kong, Y. Qi, Yanling Yang, 2009, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

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

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

[Leigh syndrome due to pyruvate dehydrogenase E1 alpha subunit gene mutation: a complicated and difficult case study].

Y. Qi, Yanling Yang, Jiangxi Xiao, 2007, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Genetic features and mechanism of Rett syndrome in Chinese population].

X. Bao, Ying Zhao, Xiaoying Zhang, 2014, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Epilepsy in children with methylmalonic acidemia: Electroclinical features and prognosis

Zhixian Yang, Yuehua Zhang, X. Bao, 2011, Brain and Development.

[Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia].

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

New variants in the CACNA1H gene identified in childhood absence epilepsy

Yan Shen, Yuehua Zhang, Yuwu Jiang, 2006, Neuroscience Letters.

Mutation screen of the gene encoding GABRB3 in Chinese patients with childhood absence epilepsy

Yan Shen, Yuehua Zhang, X. Bao, 2003, American journal of medical genetics. Part A.

The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome

Zhixian Yang, Yuehua Zhang, Xiaoyan Liu, 2018, Developmental medicine and child neurology.

NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population

P. Chan, Yuehua Zhang, Yuwu Jiang, 2014, Human Genetics.

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.

[Clinical characteristics of X-linked adrenoleukodystrophy].

Yuehua Zhang, Jiangxi Xiao, Xi-ru Wu, 2003, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Clinical and Biochemical Studies on Chinese Patients With Methylmalonic Aciduria

Yuehua Zhang, Y. Hasegawa, S. Yamaguchi, 2006, Journal of child neurology.

ARSA gene mutations in five Chinese metachromatic leukodystrophy patients.

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

Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing

Hai-po Yang, Yanling Yang, Xiaoqing Li, 2017, Scientific Reports.

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

Yan Shen, Yuehua Zhang, Yuwu Jiang, 2006, Pediatric neurology.

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.

MECP2 gene mutation analysis in Chinese patients with Rett syndrome

Yan Shen, H. Pan, Xi-ru Wu, 2002, European Journal of Human Genetics.

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.

Disseminated Encephalomyelitis-Like Central Nervous System Neoplasm in Childhood

Yun Yuan, Yuehua Zhang, Chunyu Zhang, 2014, Journal of child neurology.

Gene delivery into primary cerebral cortical neurons by lentiviral vector

X. Bao, H. Pan, Xi-ru Wu, 2006 .

Mutation screen of the GABAA receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy

Yan Shen, Yuehua Zhang, X. Bao, 2002, Neuroscience Letters.

CDKL5 in Different Atypical Rett Syndrome Variants: Description of the First Eight Patients from Spain

Liping Wei, X. Bao, Jiarui Li, 2015, Journal of Pediatric Epilepsy.

Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients

Y. Jiang, Hai-po Yang, Xi-ru Wu, 2015, Clinical genetics.

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.

KCNMA1 mutation in children with paroxysmal dyskinesia and epilepsy: Case report and literature review

X. Bao, Qingping Zhang, Yan Chen, 2017 .

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

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

[Association analysis of childhood absence epilepsy by microsatellite DNA].

Yan Shen, Yuehua Zhang, Yucai Chen, 2002, Zhonghua yi xue za zhi.

[Case-control study and transmission/disequilibrium test of childhood absence epilepsy].

Yan Shen, Yuehua Zhang, Yuwu Jiang, 2002, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[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.

T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population

Yan Shen, Yuehua Zhang, X. Bao, 2003, Neuroscience Letters.