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2. Structural analysis of NADH-cytochrome b5 reductase in relation to hereditary methemoglobinemia. Yubisui T; Murakami K; Shirabe K; Takeshita M; Zenno S; Tomatsu S; Fukumaki Y Prog Clin Biol Res; 1989; 319():107-19; discussion 120-1. PubMed ID: 2695933 [No Abstract] [Full Text] [Related]
3. Enzymopenic hereditary methemoglobinemia: a clinical/biochemical classification. Jaffé ER Blood Cells; 1986; 12(1):81-90. PubMed ID: 3539237 [TBL] [Abstract][Full Text] [Related]
4. [Hereditary methemoglobinemia due to NADH cytochrome b5 abnormality--clinical importance of the enzyme in leukocytes and platelets]. Tomita Y; Inagaki M; Taki M; Miura T; Saito N; Meguro T; Yamada K; Fujii H; Takizawa T; Miwa S Rinsho Ketsueki; 1986 Mar; 27(3):412-9. PubMed ID: 3735692 [No Abstract] [Full Text] [Related]
5. [Molecular analysis of the structure of the mutant NADH-cytochrome b5 reductase gene causing methemoglobinemia]. Kobayashi Y Fukuoka Igaku Zasshi; 1990 Jan; 81(1):41-7. PubMed ID: 2323714 [TBL] [Abstract][Full Text] [Related]
9. [Prenatal diagnosis of generalized cytochrome b5 reductase deficiency (congenital methemoglobinemia with mental retardation, type II) (author's transl)]. Kaplan JC; Junien C; Leroux A; Bamberger J; Bakouri S; Boué J; Boué A Ann Med Interne (Paris); 1981; 132(2):93-6. PubMed ID: 7235451 [TBL] [Abstract][Full Text] [Related]
10. A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis. Aalfs CM; Salieb-Beugelaar GB; Wanders RJ; Mannens MM; Wijburg FA Hum Mutat; 2000; 16(1):18-22. PubMed ID: 10874300 [TBL] [Abstract][Full Text] [Related]
11. A Thai boy with hereditary enzymopenic methemoglobinemia type II. Shotelersuk V; Tosukhowong P; Chotivitayatarakorn P; Pongpunlert W J Med Assoc Thai; 2000 Nov; 83(11):1380-6. PubMed ID: 11215870 [TBL] [Abstract][Full Text] [Related]
12. [Cell differentiation, maturation and enzyme abnormality--studies on NADH-cytochrome b5 reductase]. Takeshita M; Yubisui T Rinsho Ketsueki; 1986 Jul; 27(7):1138-44. PubMed ID: 3783996 [No Abstract] [Full Text] [Related]
13. [Genetics and biochemistry of NADH-cytochrome b5 reductase deficiency]. Shirabe K Nihon Rinsho; 1999 Sep; 57 Suppl():769-71. PubMed ID: 10543233 [No Abstract] [Full Text] [Related]
14. [Leu 72 Pro mutation in the NADH-cytochrome b5 reductase gene found in a Chinese hereditary methemoglobinemia patient]. Wu Y; Huang C; Zhu Z Zhonghua Xue Ye Xue Za Zhi; 1998 Apr; 19(4):195-7. PubMed ID: 11243135 [TBL] [Abstract][Full Text] [Related]