SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus
スポンサーリンク
概要
- 論文の詳細を見る
- Springer Japanの論文
- 2008-08-01
著者
-
Zhang Yuehua
Department Of Pediatrics Peking University First Hospital
-
QIN Jiong
Department of Pediatrics, Peking University First Hospital
-
Qin Jiong
Department Of Pediatrics Peking University First Hospital
-
Qi Yu
Peking University First Hospital
-
Wu Xiru
Peking University First Hospital
-
Yang Zhixian
Department Of Pediatrics Peking University First Hospital
-
Zhang Yongjun
Department Of Pediatric Endocrinology And Genetic Metabolism Xinhua Hospital Shanghai Second Medical
-
XU Keming
Capital Institute of Pediatrics
-
LIU Xiaoyan
Department of Pediatrics, Peking University First Hospital
-
SUN Huihui
Peking University, First Hospital
-
ZHANG Yuehua
Peking University, First Hospital
-
LIANG Jianmin
Jilin University, First Hospital
-
LIU Xiaoyan
Peking University, First Hospital
-
MA Xiuwei
Peking University, First Hospital
-
WU Husheng
Beijing Children's Hospital
-
QIN Jiong
Peking University, First Hospital
-
Ma Xiuwei
Peking University First Hospital
-
Wu Husheng
Beijing Children's Hospital
-
Liang Jianmin
Jilin University First Hospital
-
Qi Yu
Peking Union Medical College Hospital
-
SUN Huihui
Department of Pediatrics, Peking University First Hospital
-
Sun Huihui
Department Of Pediatrics Peking University First Hospital
-
Liu Xiaoyan
Department Of Pediatrics Peking University First Hospital
-
Qi Y
Department Of Pediatrics Peking University First Hospital
関連論文
- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Clinical and biochemical studies on Chinese patients with methylmalonic acidumia
- Genetic studies on SURF1 mutations in Chinese patients with mitochondrial encephalopathy
- A Clinical Survey of 65 Patients with Leigh Syndrome
- Modulating effect of hydrogen sulfide on gamma-aminobutyric acid B receptor in recurrent febrile seizures in rats
- Current Status of Research on Inborn Errors of Metabolism in China
- Screening for inborn errors of metabolism using gas chromatography-mass spectrometry
- Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center
- Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center
- Phenylketonuria in China : From Neonatal Screening to Laboratory Study
- A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood
- SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus
- Alpers syndrome with prominent white matter changes
- 4)The evolvement of work pattern in assisted reproductive technology : experiences from PUMCH(From Bulgaria and China,International Seminar 7)
- Midodrine Hydrochloride Is Effective in the Treatment of Children With Postural Orthostatic Tachycardia Syndrome
- Identification of mutations in the arginine vasopressin receptor 2 gene causing nephrogenic diabetes insipidus in Chinese patients
- Childhood absence epilepsy : Elctroclinical features and diagnostic criteria
- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria
- Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease
- Epilepsy in children with methylmalonic acidemia : Electroclinical features and prognosis