108 related articles for article (PubMed ID: 27829299)
1. Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon.
Pule GD; Ngo Bitoungui VJ; Chetcha Chemegni B; Kengne AP; Wonkam A
Hemoglobin; 2016 Nov; 40(6):377-380. PubMed ID: 27829299
[TBL] [Abstract][Full Text] [Related]
2. SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.
Pule GD; Bitoungui VJN; Chemegni BC; Kengne AP; Wonkam A
BMC Res Notes; 2017 May; 10(1):183. PubMed ID: 28499394
[TBL] [Abstract][Full Text] [Related]
3. Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.
Wonkam A; Ngo Bitoungui VJ; Vorster AA; Ramesar R; Cooper RS; Tayo B; Lettre G; Ngogang J
PLoS One; 2014; 9(3):e92506. PubMed ID: 24667352
[TBL] [Abstract][Full Text] [Related]
4. Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant.
Bhanushali AA; Himani K; Patra PK; Das BR
Hemoglobin; 2017; 41(4-6):317-320. PubMed ID: 29313433
[TBL] [Abstract][Full Text] [Related]
5. Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with β-Thalassemia and Sickle Cell Disease.
Listì F; Sclafani S; Agrigento V; Barone R; Maggio A; D'Alcamo E
Hemoglobin; 2018 Mar; 42(2):103-107. PubMed ID: 30200835
[TBL] [Abstract][Full Text] [Related]
6. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
Adeyemo T; Ojewunmi O; Oyetunji A
Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
[TBL] [Abstract][Full Text] [Related]
7. Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia.
Fong C; Menzel S; Lizarralde MA; Barreto G
Biomedica; 2015; 35(3):437-43. PubMed ID: 26849705
[TBL] [Abstract][Full Text] [Related]
8. Polymorphism in the HMOX1 gene is associated with high levels of fetal hemoglobin in Brazilian patients with sickle cell anemia.
Gil GP; Ananina G; Oliveira MB; Costa FF; Silva MJ; Santos MN; Bezerra MA; Hatzlhofer BL; Araujo AS; Melo MB
Hemoglobin; 2013; 37(4):315-24. PubMed ID: 23725037
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patients.
Adekile A; Al-Kandari M; Haider M; Rajaa M; D'Souza M; Sukumaran J
Med Princ Pract; 2007; 16(4):286-90. PubMed ID: 17541294
[TBL] [Abstract][Full Text] [Related]
11. Senegal haplotype is associated with higher HbF than Benin and Cameroon haplotypes in African children with sickle cell anemia.
Green NS; Fabry ME; Kaptue-Noche L; Nagel RL
Am J Hematol; 1993 Oct; 44(2):145-6. PubMed ID: 7505527
[No Abstract] [Full Text] [Related]
12. Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.
Wonkam A; Mnika K; Ngo Bitoungui VJ; Chetcha Chemegni B; Chimusa ER; Dandara C; Kengne AP
Br J Haematol; 2018 Jan; 180(1):134-146. PubMed ID: 29205277
[TBL] [Abstract][Full Text] [Related]
13. Hb F levels, longevity of homozygotes and clinical course of sickle cell anemia in Brazil.
Hutz MH; Salzano FM; Adams J
Am J Med Genet; 1983 Apr; 14(4):669-76. PubMed ID: 6189395
[TBL] [Abstract][Full Text] [Related]
14. Polymorphism at BCL11A compared to HBS1L-MYB loci explains less of the variance in HbF in patients with sickle cell disease in Cameroon.
Bitoungui VJ; Ngogang J; Wonkam A
Blood Cells Mol Dis; 2015 Mar; 54(3):268-9. PubMed ID: 25488618
[No Abstract] [Full Text] [Related]
15. Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features.
Al-Ali AK; Alsulaiman A; Alfarhan M; Safaya S; Vatte CB; Albuali WM; Qutub HO; Alzahrani AJ; Milton JN; Steinberg MH
Am J Hematol; 2021 Apr; 96(4):E117-E121. PubMed ID: 33460474
[No Abstract] [Full Text] [Related]
16. Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania.
Nkya S; Mwita L; Mgaya J; Kumburu H; van Zwetselaar M; Menzel S; Mazandu GK; Sangeda R; Chimusa E; Makani J
BMC Med Genet; 2020 Jun; 21(1):125. PubMed ID: 32503527
[TBL] [Abstract][Full Text] [Related]
17. Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
Makani J; Menzel S; Nkya S; Cox SE; Drasar E; Soka D; Komba AN; Mgaya J; Rooks H; Vasavda N; Fegan G; Newton CR; Farrall M; Thein SL
Blood; 2011 Jan; 117(4):1390-2. PubMed ID: 21068433
[TBL] [Abstract][Full Text] [Related]
18. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
Muszlak M; Pissard S; Badens C; Chamouine A; Maillard O; Thuret I
Hemoglobin; 2015; 39(3):156-61. PubMed ID: 25806420
[TBL] [Abstract][Full Text] [Related]
19. Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parenteral Hb F levels.
Mason KP; Grandison Y; Hayes RJ; Serjeant BE; Serjeant GR; Vaidya S; Wood WG
Br J Haematol; 1982 Nov; 52(3):455-63. PubMed ID: 6181802
[TBL] [Abstract][Full Text] [Related]
20. Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.
Mtatiro SN; Mgaya J; Singh T; Mariki H; Rooks H; Soka D; Mmbando B; Thein SL; Barrett JC; Makani J; Cox SE; Menzel S
BMC Med Genet; 2015 Feb; 16():4. PubMed ID: 25928412
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]