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5. The role of hemoglobin heme loss in Heinz body formation: studies with a partially heme-deficient hemoglobin and with genetically unstable hemoglobins. Jacob HS, Winterhalter KH. J Clin Invest; 1970 Nov; 49(11):2008-16. PubMed ID: 5475984 [Abstract] [Full Text] [Related]
6. Intermediate hemichrome formation after oxidation of three unstable hemoglobins (Freiburg, Riverdale-Bronx and Köln). Rachmilewitz EA, Harari E. Hamatol Bluttransfus; 1972 Nov; 10():241-50. PubMed ID: 4584499 [No Abstract] [Full Text] [Related]
10. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations. Margetis P, Antonelou M, Karababa F, Loutradi A, Margaritis L, Papassideri I. Blood Cells Mol Dis; 2007 Nov; 38(3):210-20. PubMed ID: 17208471 [Abstract] [Full Text] [Related]
11. Unstable hemoglobins: influence of environment on phenotypic expression of a genetic disorder. Zinkham WH, Winslow RM. Medicine (Baltimore); 1989 Sep; 68(5):309-20. PubMed ID: 2677598 [Abstract] [Full Text] [Related]
12. The thalassemic red cell membrane. Wilairat P, Kittikalayawong A, Chaicharoen S. Southeast Asian J Trop Med Public Health; 1992 Sep; 23 Suppl 2():74-8. PubMed ID: 1298998 [Abstract] [Full Text] [Related]
18. [Clinicohematologic effects of hemoglobin Altdorf (alpha 2 beta 2 135 Ala replaced by Pro)]. Marti HR, Scherrer R, Piller M. Folia Haematol Int Mag Klin Morphol Blutforsch; 1980 Sep; 107(4):648-53. PubMed ID: 6162732 [Abstract] [Full Text] [Related]
19. [Metabolic changes leading to oxidative lysis of erythrocytes maintained in a normal state in vitro]. Ataullakhanov FI, Vitvitskiĭ VM, Zhabotinskiĭ AM, Kiiatkin AB, Pichugin AV. Biokhimiia; 1986 Sep; 51(9):1562-70. PubMed ID: 3768445 [Abstract] [Full Text] [Related]