Kiyoh Tanishima

Exonic point mutations in NADH-cytochrome B5 reductase genes of homozygotes for hereditary methemoglobinemia, types I and III: putative mechanisms of tissue-dependent enzyme deficiency.

Takanori Katsube, N Sakamoto, Yasushi Kobayashi et al. · PubMed · 1991 · 40 citations

Life Sciences, Genetics, Molecular Genetics +15

High-performance liquid chromatographic determination of plasma ascorbic acid in relationship to health care

Kiyoh Tanishima · Journal of Chromatography B Biomedical Sciences and Applications · 1993 · 27 citations

Life Sciences, Biochemistry, Analytical Chemistry +10

Congenital Methaemoglobinaemia due to NADH Methaemoglobin Reductase Deficiency: Successful Treatment with Oral Riboflavin

M Hirano, Taizo Matsuki, Kiyoh Tanishima et al. · British Journal of Haematology · 1981 · 26 citations

Life Sciences, Biochemistry, Genetics +15

New variant of cytochrome b5 reductase deficiency (b5R_Kurashiki) in red cells, platelets, lymphocytes, and cultured fibroblasts with congenital methemoglobinemia, mental and neurological retardation, and skeletal anomalies

Yoshihito Yawata, Lily Ding, Kiyoh Tanishima et al. · American Journal of Hematology · 1992 · 15 citations

Life Sciences, Genetics, Hematology +11

Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.

M Takeshita, Taizo Matsuki, Kiyoh Tanishima et al. · Journal of Medical Genetics · 1982 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12