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6. [Clinical and biological forms of cytochrome b5 reductase deficiency]. Kaplan JC; Leroux A; Beauvais P C R Seances Soc Biol Fil; 1979; 173(2):368-79. PubMed ID: 159760 [TBL] [Abstract][Full Text] [Related]
7. Adipose fatty acid composition in a case of generalized deficiency of cytochrome b5 reductase in congenital methemoglobinemia with mental retardation. Hirono H Tohoku J Exp Med; 1983 Aug; 140(4):391-4. PubMed ID: 6636138 [TBL] [Abstract][Full Text] [Related]
8. New variant of cytochrome b5 reductase deficiency (b5RKurashiki) in red cells, platelets, lymphocytes, and cultured fibroblasts with congenital methemoglobinemia, mental and neurological retardation, and skeletal anomalies. Yawata Y; Ding L; Tanishima K; Tomoda A Am J Hematol; 1992 Aug; 40(4):299-305. PubMed ID: 1503085 [TBL] [Abstract][Full Text] [Related]
9. Enzymopenic hereditary methemoglobinemia: a clinical/biochemical classification. Jaffé ER Blood Cells; 1986; 12(1):81-90. PubMed ID: 3539237 [TBL] [Abstract][Full Text] [Related]
10. Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation. Takeshita M; Matsuki T; Tanishima K; Yubisui T; Yoneyama Y; Kurata K; Hara N; Igarashi T J Med Genet; 1982 Jun; 19(3):204-9. PubMed ID: 6896729 [TBL] [Abstract][Full Text] [Related]
11. Lipids of liver, kidney, spleen and muscle in a case of generalized deficiency of cytochrome b5 reductase in congenital methemoglobinemia with mental retardation. Hirono H Lipids; 1984 Jan; 19(1):60-3. PubMed ID: 6708747 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Congenital methemoglobinemia: a rare cause of cyanosis in the newborn--a case report. Da-Silva SS; Sajan IS; Underwood JP Pediatrics; 2003 Aug; 112(2):e158-61. PubMed ID: 12897322 [TBL] [Abstract][Full Text] [Related]
16. Antibody-based spot test for NADH-cytochrome b5 reductase activity for the laboratory diagnosis of congenital methemoglobinemia. Lan FH; Tang YC; Huang CH; Wu YS; Zhu ZY Clin Chim Acta; 1998 May; 273(1):13-20. PubMed ID: 9620466 [TBL] [Abstract][Full Text] [Related]
17. Lipids of myelin, white matter and gray matter in a case of generalized deficiency of cytochrome b5 reductase in congenital methemoglobinemia with mental retardation. Hirono H Lipids; 1980 Apr; 15(4):272-5. PubMed ID: 7374382 [TBL] [Abstract][Full Text] [Related]
18. NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemia. Lostanlen D; Lenoir G; Kaplan JC J Clin Invest; 1981 Jul; 68(1):279-85. PubMed ID: 6265499 [TBL] [Abstract][Full Text] [Related]