Sakamoto Osamu | Department Of Gastroenterology Ohtaatami Hospital

スポンサーリンク

概要

関連著者

もっと見る

著作論文

Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
The effects of copper-histidine therapy on brain metabolism in a patient with Menkes disease : a proton magnetic resonance spectroscopic study
Dynamic Cortical Activity during Spasms in Three Patients with West Syndrome : A Multichannel Near-infrared Spectroscopic Topography Study
Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency
Hypercalcemia due to all-trans retinoic acid therapy for acute promyelocytic leukemia : A case report of effective treatment with bisphosphonate
A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency
Novel missense mutation (R94S) in the TAZ (G4.5) gene in a Japanese patient with Barth syndrome
Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome
Malignant Paraganglioma of the Stomach
Molecular analysis of a presymptomatic case of carnitine palmitoyl transferase I (CPT I) deficiency detected by tandem mass spectrometry newborn screening in Japan
Mutation and haplotype analyses of the MUT gene in Japanese patients with methylmalonic acidemia
Vincristine-resistant Kasabach-Merritt phenomenon successfully treated with low-dose radiotherapy
Fanconi-Bickel syndrome in a 3-year-old Indian boy with a novel mutation in the GLUT2 gene
Two Novel Mutations in the Lactase Gene in a Japanese Infant with Congenital Lactase Deficiency
Cross-sectional study of bone metabolism with nutrition in adult classical phenylketonuric patients diagnosed by neonatal screening
Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome : revisited gene atlas for renumbering

もっと見る

スポンサーリンク