Wu Xiru | Department Of Pediatrics Peking University First Hospital

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概要

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著作論文

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
Current Status of Research on Inborn Errors of Metabolism in China
Alpers syndrome with prominent white matter changes
Two novel gap junction protein alpha 12 gene mutations in two Chinese patients with Pelizaeus-Merzbacher-like disease
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

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