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22. Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response. Tubman VN; Bennett CM; Luo HY; Chui DH; Heeney MM Pediatr Blood Cancer; 2007 Aug; 49(2):207-10. PubMed ID: 17551985 [TBL] [Abstract][Full Text] [Related]
23. Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell disease. Ofori-Acquah SF; Green BN; Davies SC; Nicolaides KH; Serjeant GR; Layton DM Anal Biochem; 2001 Nov; 298(1):76-82. PubMed ID: 11673898 [TBL] [Abstract][Full Text] [Related]
24. Transfusion medicine illustrated. Hemoglobin D after a red-cell exchange for sickle-cell disease. Brecher ME; Park YA; Whinna HC; McClannan LS; Afenyi-Annan A Transfusion; 2008 Nov; 48(11):2277-8. PubMed ID: 19054375 [No Abstract] [Full Text] [Related]
25. [Diagnosis and screening of sickle cell disease]. Wajcman H Rev Prat; 2004 Sep; 54(14):1543-7. PubMed ID: 15558963 [TBL] [Abstract][Full Text] [Related]
26. Clinical expression of sickle cell anemia in the newborn. van Wijgerden JA South Med J; 1983 Apr; 76(4):477-80. PubMed ID: 6188222 [TBL] [Abstract][Full Text] [Related]
27. Hemoglobin G trait and S trait in the same patient. LeCrone CN; Jones JA; Detter JC Am J Med Technol; 1983 Mar; 49(3):165-7. PubMed ID: 6837616 [TBL] [Abstract][Full Text] [Related]
28. Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia. Bertles JF; Milner PF J Clin Invest; 1968 Aug; 47(8):1731-41. PubMed ID: 5666109 [TBL] [Abstract][Full Text] [Related]
29. Sickling in Tanzania. Mitchell R; Fupi F East Afr Med J; 1972 Sep; 49(9):638-42. PubMed ID: 4656959 [No Abstract] [Full Text] [Related]
30. [Disease caused by sickle cell anemia and hemoglobin D-Punjab. 3d case found in Venezuela]. Guevara JM; Arends-Merino A; Arends T Sangre (Barc); 1985; 30(2):185-9. PubMed ID: 4012519 [No Abstract] [Full Text] [Related]
31. Sickling syndromes in children. Honig GR Adv Pediatr; 1976; 23():271-313. PubMed ID: 795281 [TBL] [Abstract][Full Text] [Related]
32. Cardiorenal risk prevalence in sickle cell hemoglobinopathy. Abo-Zenah H; Moharram M; El Nahas AM Nephron Clin Pract; 2009; 112(2):c98-c106. PubMed ID: 19390209 [TBL] [Abstract][Full Text] [Related]
33. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family]. Dahmane-Arbane M; Blouquit Y; Arous N; Bardakdjian J; Benamani M; Riou J; Benabadji M; Rosa J; Galacteros F Nouv Rev Fr Hematol (1978); 1987; 29(5):317-20. PubMed ID: 3438164 [TBL] [Abstract][Full Text] [Related]
34. [Circulatory disturbance in the area supplied by the Art. vertebro basilaris in a case of sickle-cell trait (Hb AS)]. Fischer M; Weissmann A; Tschabitscher H Wien Klin Wochenschr; 1972 Nov; 84(45):728-30. PubMed ID: 4634672 [No Abstract] [Full Text] [Related]
35. Red cell distribution width in sickle cell disease. Webster P; Castro O Ann Clin Lab Sci; 1986; 16(4):274-7. PubMed ID: 3740796 [TBL] [Abstract][Full Text] [Related]
37. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin. Shokrani M; Terrell F; Turner EA; Aguinaga MD Ann Clin Lab Sci; 2000 Apr; 30(2):191-4. PubMed ID: 10807164 [TBL] [Abstract][Full Text] [Related]
38. Sickle-cell thalassaemia disease in Sudanese. Ibrahim SA East Afr Med J; 1970 Jan; 47(1):47-9. PubMed ID: 5436179 [No Abstract] [Full Text] [Related]
39. Hb S/Hb Lepore with mild sickling symptoms: a hemoglobin variant with mostly delta-chain sequences ameliorates sickle-cell disease. Fairbanks VF; McCormick DJ; Kubik KS; Rezuke WN; Black D; Ochaney MS; Schwartz D Am J Hematol; 1997 Feb; 54(2):164-5. PubMed ID: 9034293 [TBL] [Abstract][Full Text] [Related]
40. A simple and inexpensive screening test for sickle hemoglobin. Greenberg MS; Harvey HA; Morgan C N Engl J Med; 1972 May; 286(21):1143-4. PubMed ID: 5019642 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]