Epilepsy in children with methylmalonic acidemia : Electroclinical features and prognosis
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概要
- 論文の詳細を見る
- 2011-10-01
著者
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Yang Yanling
Department Of Neurology Peking University First Hospital
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Zhang Yuehua
Department Of Pediatrics Peking University First Hospital
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BAO Xinhua
Department of Pediatrics, Peking University First Hospital
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WU Xiru
Department of Pediatrics, Peking University First Hospital
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YANG Zhixian
Department of Pediatrics, Peking University First Hospital
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Qin Jiong
Department Of Pediatrics Peking University First Hospital
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Bao Xinhua
Department Of Pediatrics Peking University First Hospital
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Yang Zhixian
Department Of Pediatrics Peking University First Hospital
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LIU Xiaoyan
Department of Pediatrics, Peking University First Hospital
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Wu Xiru
Department Of Pediatrics Peking University First Hospital
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MA Xiuwei
Department of Pediatrics, Peking University First Hospital
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Ma Xiuwei
Department Of Pediatrics Peking University First Hospital
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Liu Xiaoyan
Department Of Pediatrics Peking University First Hospital
関連論文
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- Clinical and biochemical studies on Chinese patients with methylmalonic acidumia
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- SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus
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- Childhood absence epilepsy : Elctroclinical features and diagnostic criteria
- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)
- Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease
- Epilepsy in children with methylmalonic acidemia : Electroclinical features and prognosis
- Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutations