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7. [3 cases of beta-thalassodrepanocytosis with highly elevated levels of alkali-resistant hemoglobin on a Congolese family]. Gatti F; Nicolas J; Van Ros G; Vandepitte J Ann Soc Belges Med Trop Parasitol Mycol; 1967; 47(4):313-29. PubMed ID: 5633978 [No Abstract] [Full Text] [Related]
8. [Hemoglobinopathies: molecular, genetic and clinical aspects]. de Araújo JT; Ribeiro VS; de Araújo RA Rev Hosp Clin Fac Med Sao Paulo; 1987; 42(6):260-6. PubMed ID: 3455557 [No Abstract] [Full Text] [Related]
9. SPLENECTOMY FOR HYPERSPLENISM IN SICKLE CELL ANEMIA. EGDAHL RH; MARTIN WW; HILKOVITZ G JAMA; 1963 Nov; 186():745-8. PubMed ID: 14078086 [No Abstract] [Full Text] [Related]
10. SPLENECTOMY FOR HYPERSPLENISM IN SICKLE CELL ANEMIA. EGDAHL RH; MARTIN WW; HILKOVITZ G JAMA; 1963 Nov; 186():745-8. PubMed ID: 14065362 [No Abstract] [Full Text] [Related]
11. Hemoglobin D Los Angeles in two Caucasian families: hemoglobin SD disease and hemoglobin D thalassemia. Schneider RG; Ueda S; Alperin JB; Levin WC; Jones RT; Brimhall B Blood; 1968 Aug; 32(2):250-9. PubMed ID: 5672850 [No Abstract] [Full Text] [Related]
12. Splenic platelet pooling as a cause of "hypersplenic" thrombocytopenia. Aster RH Trans Assoc Am Physicians; 1965; 78():362-73. PubMed ID: 5864981 [No Abstract] [Full Text] [Related]
13. Hemolytic anemias associated with hemoglobinopathies. Lessin LS; Klug P Mod Treat; 1971 May; 8(2):352-78. PubMed ID: 4940518 [No Abstract] [Full Text] [Related]
14. Comparison of sickle cell beta o-thalassemia and sickle cell beta +-thalassemia in black populations. Serjeant GR; Serjeant BE Birth Defects Orig Artic Ser; 1982; 18(7):223-9. PubMed ID: 7159733 [No Abstract] [Full Text] [Related]
15. [SA hemoglobinosis and osteomyelitis]. Cornet A; Brumpt LC; Terris G; Coumbaras A Sem Hop; 1969 May; 45(22):1533-9. PubMed ID: 4308641 [No Abstract] [Full Text] [Related]
16. Genetics and clinical manifestations of hemoglobinopathies. McCurdy PR Ann Clin Lab Sci (1971); 1971; 1(3):231-5. PubMed ID: 5154972 [No Abstract] [Full Text] [Related]
17. Splenic complications of the sickling syndromes and the role of splenectomy. Al-Salem AH; Naserullah Z; Qaisaruddin S; Al-Abkari H; Al-Faraj A; Yassin YM J Pediatr Hematol Oncol; 1999; 21(5):401-6. PubMed ID: 10524454 [TBL] [Abstract][Full Text] [Related]
18. Modification of hemoglobin H disease by sickle trait. Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366 [TBL] [Abstract][Full Text] [Related]
19. A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassaemia. Weatherall DJ; Clegg JB; Blankson J; McNeil JR Br J Haematol; 1969 Dec; 17(6):517-26. PubMed ID: 5357741 [No Abstract] [Full Text] [Related]