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Department Of Pediatrics Peking University First Hospital | 論文
- Increase of Lipid Hydroperoxides in the Rat Liver and Kidney after Administering Ferric Nitrilotriacetate
- 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
- The effects of antiepileptic drugs on spatial learning and hippocampal protein kinase C γin immature rats
- 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
- Two novel gap junction protein alpha 12 gene mutations in two Chinese patients with Pelizaeus-Merzbacher-like disease
- Study on the reference values of serum lipids in children aged 3-18 years old in Beijing, China
- Childhood absence epilepsy : Elctroclinical features and diagnostic criteria
- Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bε (eIF2Bε) identified in Chinese patients with vanishing white matter disease
- 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
- Meta-Analysis of Randomized Controlled Trials on Treatment of Pulmonary Arterial Hypertension
- 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
- Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay
- 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
- Increased Expression of Netrin-1 and Its Deleted in Colorectal Cancer Receptor in Human Diseased Lumbar Intervertebral Disc Compared With Autopsy Control