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28. Unstable hemoglobin as a cause of congenital hemolytic anemia. Singh R; Sudarsanam A Indian Pediatr; 1996 Jul; 33(7):587-9. PubMed ID: 8979570 [No Abstract] [Full Text] [Related]
29. Transfusion therapy in congenital hemolytic anemias. Sharon BI Hematol Oncol Clin North Am; 1994 Dec; 8(6):1053-86. PubMed ID: 7860437 [TBL] [Abstract][Full Text] [Related]
30. Hemoglobin Hammersmith [beta42 (CD1) Phe --> Ser] in a Brazilian girl with congenital Heinz body hemolytic anemia. Sonati MF; Kimura EM; Abreu CF; Oliveira DM; Pinheiro VR; Costa FF Pediatr Blood Cancer; 2006 Nov; 47(6):855-6; author reply 857-8. PubMed ID: 16619220 [No Abstract] [Full Text] [Related]
31. Hemoglobinopathies in childhood (a study of 51 cases). Giri DD; Patra SB; Patel RZ Indian J Pathol Microbiol; 1984 Apr; 27(2):81-9. PubMed ID: 6511037 [No Abstract] [Full Text] [Related]
32. Hemoglobin SE disease: a concise review. Masiello D; Heeney MM; Adewoye AH; Eung SH; Luo HY; Steinberg MH; Chui DH Am J Hematol; 2007 Jul; 82(7):643-9. PubMed ID: 17278112 [TBL] [Abstract][Full Text] [Related]
33. [Diagnosis and gene analysis of congenital hemolytic anemia]. Ideguchi H Rinsho Byori; 2006 Jun; 54(6):593-600. PubMed ID: 16872009 [TBL] [Abstract][Full Text] [Related]
35. Congenital hemolytic anemias. Fernbach DJ Am J Med Technol; 1969 Apr; 35(4):209-18. PubMed ID: 5779414 [No Abstract] [Full Text] [Related]
36. Innovative parameters RET-Y, sTfR, and sTfR-F index in patients with microcytic, hypochromic anemia--their special value for hemoglobinopathies. Agorasti A; Trivellas T; Papadopoulos V; Konstantinidou D Lab Hematol; 2007; 13(2):63-8. PubMed ID: 17573284 [TBL] [Abstract][Full Text] [Related]
37. [S hemoglobin gene carrier born to a mother with microdrepanocytic disease. A rare occurrence of maternal survival and of the possibility of carrying a pregnancy to term]. Ingiulla A; D'Asero G Riv Ostet Ginecol; 1968 May; 23(5):368-73. PubMed ID: 5748321 [No Abstract] [Full Text] [Related]
38. Hemolytic anaemia due to unstable hemoglobin arising from spontaneous mutation--a case report. Dash S; Menon S; Marwaha RK Indian J Pathol Microbiol; 2006 Apr; 49(2):269-70. PubMed ID: 16933736 [TBL] [Abstract][Full Text] [Related]
39. [Minkowski-Chauffard disease. Apropos of a triple familial case]. Giard P; Routier G; Lamoril JL J Sci Med Lille; 1969 Dec; 87(12):735-43. PubMed ID: 5403370 [No Abstract] [Full Text] [Related]
40. [Congenital dyserythropoiesis with erythroblastic polyploidy. Report of a variety found in Argentinian Mesopotamia (author's transl)]. Accame EA; de Tezanos Pinto M Sangre (Barc); 1981; 26(5-A):545-55. PubMed ID: 7323912 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]