Sakura Nobuo | Department Of Pediatrics Faculty Of Medicine Hiroshima University
スポンサーリンク
概要
関連著者
-
Sakura Nobuo
Department Of Pediatrics Faculty Of Medicine Hiroshima University
-
SAKURA NOBUO
Department of Pediatrics, Hiroshima University School of Medicine
-
ONO Hiroaki
Department of Liberal Arts, Osaka Technical College
-
Sakura Nobuo
Department Of Pediatrics Hiroshima University School Of Medicine
-
Ono Hiroaki
Department Of Liberal Arts And Science Setsunan University
-
Ono Hiroaki
Department of Chemistry, Faculty of Science, Hiroshima University
-
Ueda Kazuhiro
Department Of Pediatrics Hiroshima University School Of Medicine
-
Ueda Kazuhiro
Department Of Energy And Hydrocarbon Chemistry Graduate School Of Engineering Kyoto University
-
UEDA Kazuhiro
Department of Pediatrics, Graduate School of Biomedical Sciences, Hiroshima University
-
Ono Hiroaki
Department Of Pediatrics Hiroshima University Graduate School Of Biomedical Sciences
著作論文
- 食品中のベタインとホモシステイン濃度
- A Case of MELAS : Hyperperfused Lesions Detected by Non-invasive Perfusion-weighted MR Imaging
- Novel mutation of methylmalonyl-CoA mutase gene causing the mut^0 form of methylmalonic acidemia in a Japanese girl
- Enzymatic diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by detecting 2-octenoyl-CoA production using high-performance liquid chromatography : A practical confirmatory test for tandem mass spectrometry newborn screening in Japan
- ホモシスチン尿症の新生児スクリーニング対するHPLC法に濾紙血中の総ホモシステイン濃度の測定
- The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsants
- Stable-isotope dilution gas chromatography-mass spectrometric measurement of 3-hydroxyglutaric acid, glutaric acid and related metabolites in body fluids of patients with glutaric aciduria type 1 found in newborn screening
- Failure of cortisone acetate therapy in 21-hydroxylase deficiency in early infancy
- Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia
- Limited effectiveness of betaine therapy for cystathionine β synthase deficiency