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5. Hereditary methemoglobinemia due to diaphorase deficiency. Report of a case of heterozygote presenting with cyanosis after birth. Lo SS; Hitzig WH; Marti HR Acta Haematol; 1970; 43(3):177-83. PubMed ID: 4986140 [No Abstract] [Full Text] [Related]
6. METHAEMOGLOBIN LEVEL AND ITS RELATION TO THE STABILITY OF ERYTHROCYTIC REDUCED GLUTATHIONE IN THALASSAEMIA SYNDROME. SWARUP S; GHOSH SK; CHATTERJEA JB Indian J Med Res; 1964 Mar; 52():273-8. PubMed ID: 14134590 [No Abstract] [Full Text] [Related]
7. Unstable variant of NADH methemoglobin reductase in Puerto Ricans with hereditary methemoglobinemia. Schwartz JM; Paress PS; Ross JM; DiPillo F; Rizek R J Clin Invest; 1972 Jun; 51(6):1594-601. PubMed ID: 4336945 [TBL] [Abstract][Full Text] [Related]
8. HEREDITARY DIAPHORASE DEFICIENCY AND METHEMOGLOBINEMIA. CAWEIN M; BEHLEN CH; LAPPAT EJ; COHN JE Arch Intern Med; 1964 Apr; 113():578-85. PubMed ID: 14109019 [No Abstract] [Full Text] [Related]
9. Homozygous hemoglobin D Punjab. Ozsoylu S Acta Haematol; 1970; 43(6):353-9. PubMed ID: 4991321 [No Abstract] [Full Text] [Related]
10. The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia. Kim DS; Baek HJ; Kim BR; Yoon BA; Lee JH; Kook H Yonsei Med J; 2020 Dec; 61(12):1064-1067. PubMed ID: 33251782 [TBL] [Abstract][Full Text] [Related]
11. Hereditary methemoglobinemic cyanosis due to diaphorase deficiency in three successive generations. Ozsoylu S Acta Haematol; 1967; 37(5):276-83. PubMed ID: 4963515 [No Abstract] [Full Text] [Related]
12. [Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes]. Jabłońska-Skwiecińska E; Wierzbicka M; Kubicka K Pediatr Pol; 1989 Jan; 64(1):53-9. PubMed ID: 2812907 [TBL] [Abstract][Full Text] [Related]
13. Hereditary methemoglobinemia as a cause of cyanosis during anesthesia. Gabel RA; Bunn HF Anesthesiology; 1974 May; 40(5):516-8. PubMed ID: 4822398 [No Abstract] [Full Text] [Related]
14. [Recessive congenital methemoglobinemia. Clinical and laboratory study of one case]. Hermabessiere C; Poisson C; Leveque B; Leroux A; Kaplan JC Ann Pediatr (Paris); 1976 Sep; 23(8-9):509-13. PubMed ID: 16104185 [No Abstract] [Full Text] [Related]
16. [Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase]. Schmidt K; Faber K; Heni F Blut; 1974 Jul; 29(1):43-9. PubMed ID: 4367854 [No Abstract] [Full Text] [Related]
17. [Congenital methemoglobinemia found in an adult. Case report]. Szyguła E; Jacheć W; Poloński L; Kuśnierz B Pol Arch Med Wewn; 1995 Jun; 93(6):520-4. PubMed ID: 7491353 [TBL] [Abstract][Full Text] [Related]
19. [Cyanosis. Hemoglobin M as the cause in 2 unrelated Norwegian families]. Finne PH; Stavem P Tidsskr Nor Laegeforen; 1973 Jun; 93(16):1226-9. PubMed ID: 4752595 [No Abstract] [Full Text] [Related]
20. Haemoglobin M in a Cape coloured family. Botha MC; Fisher AJ; van Lingen WH S Afr Med J; 1967 Mar; 41(11):263-7. PubMed ID: 6023247 [No Abstract] [Full Text] [Related] [Next] [New Search]