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Department of Pediatrics, Peking University First Hospital | 論文
- Hydrogen Sulfide Regulates Cardiac Function and Structure in Adriamycin-Induced Cardiomyopathy
- 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
- Key molecular events in puromycin aminonucleoside nephrosis rats
- Meta-Analysis of Randomized Controlled Trials on the Treatment of Pulmonary Arterial Hypertension : Reply
- Regulatory Effect of Hydrogen Sulfide on Vascular Collagen Content in Spontaneously Hypertensive Rats
- Investigation on the Giant Magnetoimpedance of Fe_Zr_7B_4Al_x (x = 0 and 2.5) Nanocrystalline Ribbons
- 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
- Using denaturing HPLC for SNP discovery and genotyping, and establishing the linkage disequilibrium pattern for the all-trans-retinol dehydrogenase (RDH8) gene
- The effects of antiepileptic drugs on spatial learning and hippocampal protein kinase C γin immature rats
- Improved therapeutic efficacy against murine carcinoma by combining honokiol with gene therapy of PNAS-4, a novel pro-apoptotic gene
- Simultaneous quantitation of aconitine, mesaconitine, hypaconitine, benzoylaconine, benzoylmesaconine and benzoylhypaconine in human plasma by liquid chromatography-tandem mass spectrometry and pharmacokinetics evaluation of "SHEN-FU" injectable powder
- 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