Xiaoyan Liu

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.

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

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

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

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

Genetic (idiopathic) epilepsy with photosensitive seizures includes features of both focal and generalized seizures

Zhixian Yang, Yuehua Zhang, Yuwu Jiang, 2018, Scientific Reports.

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

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

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.

Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies

Hui Xiong, Hai-po Yang, Xiaoyan Liu, 2022, Seizure.

Childhood absence epilepsy: Elctroclinical features and diagnostic criteria

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

[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.

Epilepsy in children with methylmalonic acidemia: Electroclinical features and prognosis

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

Clinical and electrophysiological characteristics of startle epilepsy in childhood

Zhixian Yang, Yuehua Zhang, X. Bao, 2010, Clinical Neurophysiology.

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

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

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.

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

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

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.

Neck myoclonia with absence seizures: report of 3 cases.

Zhixian Yang, Yuwu Jiang, Xiaoyan Liu, 2009, Journal of child neurology.

Subtotal hemispherotomy for intractable lesional hemispheric epilepsy without hemiparesis in children

Qingzhu Liu, Yuwu Jiang, Xiaoyan Liu, 2022, Epilepsy Research.

Surgical treatment of children with drug-resistant epilepsy involving the Rolandic area.

Qingzhu Liu, Xiaoyan Liu, T. Ji, 2021, Epileptic disorders.

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.

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

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

[Surgery for pediatric intractable epilepsy due to posterior quadrantic cortical dysplasia].

Qingzhu Liu, Yuwu Jiang, Xiaoyan Liu, 2017, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

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.

Disconnection Surgery in Pediatric Epilepsy: A Single Center's Experience With 185 Cases.

Qingzhu Liu, Xiaoyan Liu, Hao Yu, 2023, Neurosurgery.

Epilepsy and Narcolepsy-Cataplexy in a Child

F. Han, Zhixian Yang, Xiaoyan Liu, 2012, Journal of child neurology.

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

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

Distinctive epileptogenic networks for parietal operculum seizures

O. David, Wenjing Zhou, Haixiang Wang, 2019, Epilepsy & Behavior.

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.

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.

[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.

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.