Current Status of Research on Inborn Errors of Metabolism in China

スポンサーリンク

概要

論文の詳細を見る
2003-07-18

著者

関連論文

Clinical and biochemical studies on Chinese patients with methylmalonic acidumia
Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening
Down-Regulation of Endogenous Hydrogen Sulfide Pathway in Pulmonary Hypertension and Pulmonary Vascular Structural Remodeling Induced by High Pulmonary Blood Flow in Rats
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
Effect of L-Arginine on Collagen of High Flow-Induced Pulmonary Arterial Remodeling
Current Status of Research on Inborn Errors of Metabolism in China
Physiologic neurocirculatory patterns in the head-up tilt test in children with orthostatic intolerance
Meta-Analysis of Randomized Controlled Trials on the Treatment of Pulmonary Arterial Hypertension : Reply
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
Midodrine Hydrochloride Is Effective in the Treatment of Children With Postural Orthostatic Tachycardia Syndrome
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
Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
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
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

もっと見る

スポンサーリンク