Xiuwei Ma

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

Huihui Sun, Yuehua Zhang, Jianmin Liang et al. · Journal of Human Genetics · 2008 · 67 citations · Full text

Generalized Epilepsy, Mendelian Disorder, Genetic Disorder +8

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

Huihui Sun, Yuehua Zhang, Xiaoyan Liu et al. · Journal of Human Genetics · 2010 · 44 citations · Full text

Dravet Syndrome, Allelic Variant, Scn1a Mutation +10

Childhood absence epilepsy: Elctroclinical features and diagnostic criteria

Xiuwei Ma, Yuehua Zhang, Zhixian Yang et al. · Brain and Development · 2010 · 29 citations

Neuropsychological Functioning, Disability, Pediatrics +4

Three intellectual disability-associated de novo mutations in MECP2 identified by trio-WES analysis

Yi Gu, Bingwu Xiang, Lina Zhu et al. · BMC Medical Genetics · 2020 · 22 citations · Full text

Perinatal Occipital Lobe Injury in Children: Analysis of Twenty-One Cases

Sanmei Wang, Chang-shuan Yang, Yu Hou et al. · Pediatric Neurology · 2012 · 16 citations

Pediatric Neurosurgery, Pediatrics, Pediatric Traumatic Brain Injury +4