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22. Prenatal diagnosis of sickle-cell anemia and alpha G Philadelphia. Study of a Fetus also at risk for H b S/beta+-thalassemia. Alter BP; Friedman S; Hobbins JC; Mahoney MJ; Sherman AS; McSweeney JF; Nathan DG; Schwartz E N Engl J Med; 1976 May; 294(19):1040-1. PubMed ID: 3736 [No Abstract] [Full Text] [Related]
23. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene. Wong SC; Ali MA; Boyadjian SE Acta Haematol; 1981; 65(3):157-63. PubMed ID: 6165216 [TBL] [Abstract][Full Text] [Related]
24. Sickle-delta beta thalassemia: mild sickling disorder with serious morbidity in pregnancy. Cohen AW; Russell MO; Mennuti MT Obstet Gynecol; 1981 Jul; 58(1):127-30. PubMed ID: 7243140 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. Alpha-thalassemia in a pool of individuals of Eti-Turk origin with hemoglobin S (Hb S). Jama H; Gürgey A; Altay C Turk J Pediatr; 1987; 29(1):1-14. PubMed ID: 3433374 [No Abstract] [Full Text] [Related]
27. Homozygous alpha thalassemia 2 causing a false negative solubility test in sickle cell trait. Krauss JS; Hahn DA Clin Chem; 1981 Jun; 27(6):1146. PubMed ID: 7237752 [No Abstract] [Full Text] [Related]
28. Comparison of homozygous sickle cell disease in northern Greece and Jamaica. Christakis J; Vavatsi N; Hassapopoulou H; Papadopoulou M; Mandraveli K; Loukopoulos D; Morris JS; Serjeant BE; Serjeant GR Lancet; 1990 Mar; 335(8690):637-40. PubMed ID: 1690325 [TBL] [Abstract][Full Text] [Related]
29. The spleen in sickle cell disease and thalassemia. Powars DR; Pegelow CH Am J Pediatr Hematol Oncol; 1979; 1(4):343-53. PubMed ID: 397779 [No Abstract] [Full Text] [Related]
30. Heterozygous thalassemia and pregnancy: a twenty-five year experience. Morrison JC; Roe PL; Stahl RL; Whybrew WD; Bucovaz ET; Wiser WL; Kraus AP; Fish SA J Reprod Med; 1973 Jul; 11(1):35-9. PubMed ID: 4717612 [No Abstract] [Full Text] [Related]
31. [Haemoglobin S/beta thalassaemia in a Greek family: a case study (author's transl)]. Fischer M; Hopmeier P; Lurf M; Neuwald C; Lachmann D Wien Klin Wochenschr; 1979 Jan; 91(2):45-8. PubMed ID: 433279 [TBL] [Abstract][Full Text] [Related]
32. The painful crisis of homozygous sickle cell disease. A study of the risk factors. Baum KF; Dunn DT; Maude GH; Serjeant GR Arch Intern Med; 1987 Jul; 147(7):1231-4. PubMed ID: 3606281 [TBL] [Abstract][Full Text] [Related]
33. A rare case of a compound heterozygote hemoglobin S/hemoglobin Fannin-Lubbock-I individual. Is it a sickling disorder? Burns NK; Risin SA Lab Hematol; 2010 Jun; 16(2):26-7. PubMed ID: 20534428 [No Abstract] [Full Text] [Related]
34. Sickle cell disease as a cause of osteonecrosis of the femoral head. Milner PF; Kraus AP; Sebes JI; Sleeper LA; Dukes KA; Embury SH; Bellevue R; Koshy M; Moohr JW; Smith J N Engl J Med; 1991 Nov; 325(21):1476-81. PubMed ID: 1944426 [TBL] [Abstract][Full Text] [Related]
35. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia. Kan YW Schweiz Med Wochenschr Suppl; 1991; 43():51-4. PubMed ID: 1726857 [TBL] [Abstract][Full Text] [Related]
36. Characteristics of menstruation in sickle cell disease. Samuels-Reid J; Scott RB Fertil Steril; 1985 Jan; 43(1):139-41. PubMed ID: 3965308 [TBL] [Abstract][Full Text] [Related]
37. Management of sickle cell/beta thalassemia patient with severe odontogenic infection. Ziccardi VB; Feretti A; Schneider W N Y State Dent J; 1996 Oct; 62(8):28-32. PubMed ID: 8909043 [TBL] [Abstract][Full Text] [Related]
38. Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab. Torres LS; Okumura JV; Belini-Júnior É; Oliveira RG; Nascimento PP; Silva DG; Lobo CL; Oliani SM; Bonini-Domingos CR Hemoglobin; 2016 Sep; 40(5):356-358. PubMed ID: 27535451 [TBL] [Abstract][Full Text] [Related]