267 related articles for article (PubMed ID: 22017641)
21. DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.
Cardoso GL; Diniz IG; Silva AN; Cunha DA; Silva Junior JS; Uchôa CT; Santos SE; Trindade SM; Cardoso Mdo S; Guerreiro JF
Blood Cells Mol Dis; 2014 Dec; 53(4):176-9. PubMed ID: 25084696
[TBL] [Abstract][Full Text] [Related]
22. The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.
Belisário AR; Sales RR; Silva CM; Velloso-Rodrigues C; Viana MB
Hemoglobin; 2016 Jun; 40(3):215-9. PubMed ID: 27117574
[TBL] [Abstract][Full Text] [Related]
23. Fetal hemoglobin in sickle cell anemia: a glass half full?
Steinberg MH; Chui DH; Dover GJ; Sebastiani P; Alsultan A
Blood; 2014 Jan; 123(4):481-5. PubMed ID: 24222332
[TBL] [Abstract][Full Text] [Related]
24. The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations.
Dimovski AJ; Efremov DG; Gu LH; Huisman TH
Br J Haematol; 1994 Jun; 87(2):353-6. PubMed ID: 7524623
[TBL] [Abstract][Full Text] [Related]
25. Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern Gabon.
Mombo LE; Mabioko-Mbembo G; Kassa-Kassa RF; Ontsitsagui E; Mboui-Ondo S; Nzé-Kamsi L; Nkoghé D; Elion J
Hematology; 2017 Sep; 22(8):508-513. PubMed ID: 28228042
[TBL] [Abstract][Full Text] [Related]
26. Osteomyelitis in sickle cell haemoglobinopathy with elevated fetal haemoglobin.
Narchi H
Ann Trop Paediatr; 2000 Mar; 20(1):70-5. PubMed ID: 10824218
[TBL] [Abstract][Full Text] [Related]
27. Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia.
Pembrey ME; Wood WG; Weatherall DJ; Perrine RP
Br J Haematol; 1978 Nov; 40(3):415-29. PubMed ID: 749927
[TBL] [Abstract][Full Text] [Related]
28. Increased HbF in sickle cell anemia is determined by a factor linked to the beta S gene from one parent.
Milner PF; Leibfarth JD; Ford J; Barton BP; Grenett HE; Garver FA
Blood; 1984 Jan; 63(1):64-72. PubMed ID: 6197115
[TBL] [Abstract][Full Text] [Related]
29. Effect of Swiss-type heterocellular HPFH from XmnI-Gγ and HBBP1 polymorphisms on HbF, HbE, MCV and MCH levels in Thai HbE carriers.
Kerdpoo S; Limweeraprajak E; Tatu T
Int J Hematol; 2014 Mar; 99(3):338-44. PubMed ID: 24474642
[TBL] [Abstract][Full Text] [Related]
30. Fetal hemoglobin in sickle cell anemia.
Akinsheye I; Alsultan A; Solovieff N; Ngo D; Baldwin CT; Sebastiani P; Chui DH; Steinberg MH
Blood; 2011 Jul; 118(1):19-27. PubMed ID: 21490337
[TBL] [Abstract][Full Text] [Related]
31.
Gardner K; Fulford T; Silver N; Rooks H; Angelis N; Allman M; Nkya S; Makani J; Howard J; Kesse-Adu R; Rees DC; Stuart-Smith S; Yeghen T; Awogbade M; Sangeda RZ; Mgaya J; Patel H; Newhouse S; Menzel S; Thein SL
Blood Adv; 2018 Feb; 2(3):235-239. PubMed ID: 29437638
[TBL] [Abstract][Full Text] [Related]
32. rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Chaouch L; Moumni I; Ouragini H; Darragi I; Kalai M; Chaouachi D; Boudrigua I; Hafsia R; Abbes S
Hematology; 2016 Aug; 21(7):425-9. PubMed ID: 27077760
[TBL] [Abstract][Full Text] [Related]
33. β-globin gene cluster haplotypes in sickle cell patients from Panamá.
Rusanova I; Cossio G; Moreno B; Javier Perea F; De Borace RG; Perea M; Escames G; Acuña-Castroviejo D
Am J Hum Biol; 2011; 23(3):377-80. PubMed ID: 21387457
[TBL] [Abstract][Full Text] [Related]
34. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease.
Maier-Redelsperger M; Noguchi CT; de Montalembert M; Rodgers GP; Schechter AN; Gourbil A; Blanchard D; Jais JP; Ducrocq R; Peltier JY
Blood; 1994 Nov; 84(9):3182-8. PubMed ID: 7524767
[TBL] [Abstract][Full Text] [Related]
35. Frequency of foetal haemoglobin and haemoglobin values in various haemoglobin genotypes in Calabar, Nigeria.
Uko EK; Useh MF; Gwanmesia FN
East Afr Med J; 1997 Dec; 74(12):809-11. PubMed ID: 9557428
[TBL] [Abstract][Full Text] [Related]
36. Interaction of heterocellular hereditary persistence of foetal haemoglobin with beta thalassaemia and sickle cell anaemia.
Wood WG; Weatherall DJ; Clegg JB
Nature; 1976 Nov; 264(5583):247-9. PubMed ID: 1004547
[No Abstract] [Full Text] [Related]
37. (delta beta) zero thalassemia of the Southern Italian type. Its geographical origin and interaction with the sickle cell gene.
Trent RJ; Svirklys L; Harris MG; Hocking DR; Kronenberg H
Pathology; 1986 Jan; 18(1):117-22. PubMed ID: 2425331
[TBL] [Abstract][Full Text] [Related]
38. Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia trait.
Garner C; Dew TK; Sherwood R; Rees D; Thein SL
Br J Haematol; 2003 Oct; 123(2):353-8. PubMed ID: 14531920
[TBL] [Abstract][Full Text] [Related]
39. Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population.
Mayuranathan T; Rayabaram J; Das R; Arora N; Edison ES; Chandy M; Srivastava A; Velayudhan SR
Eur J Haematol; 2014 Jun; 92(6):514-20. PubMed ID: 24471888
[TBL] [Abstract][Full Text] [Related]
40. Hereditary persistence of hemoglobin F is protective against red cell sickling. A case report and brief review.
Sokolova A; Mararenko A; Rozin A; Podrumar A; Gotlieb V
Hematol Oncol Stem Cell Ther; 2019 Dec; 12(4):215-219. PubMed ID: 29079125
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
