These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Enzymopenic hereditary methemoglobinemia: a clinical/biochemical classification. Jaffé ER Blood Cells; 1986; 12(1):81-90. PubMed ID: 3539237 [TBL] [Abstract][Full Text] [Related]
6. 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]
10. Metoclopramide-induced methemoglobinemia in a patient with co-existing deficiency of glucose-6-phosphate dehydrogenase and NADH-cytochrome b5 reductase: failure of methylene blue treatment. Karadsheh NS; Shaker Q; Ratroat B Haematologica; 2001 Jun; 86(6):659-60. PubMed ID: 11418378 [No Abstract] [Full Text] [Related]
11. 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]
12. [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]