201 related articles for article (PubMed ID: 22188117)
1. Phenotype and genotype frequency of β-thalassemia and sickle cell disease carriers in Halkidiki, Northern Greece.
Kalleas C; Anagnostopoulos K; Sinopoulou K; Delaki E; Margaritis D; Bourikas G; Tsatalas C; Kortsaris A; Tentes I
Hemoglobin; 2012; 36(1):64-72. PubMed ID: 22188117
[TBL] [Abstract][Full Text] [Related]
2. Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece.
Papachatzopoulou A; Kourakli A; Stavrou EF; Fragou E; Vantarakis A; Patrinos GP; Athanassiadou A
Hemoglobin; 2010; 34(4):333-42. PubMed ID: 20642331
[TBL] [Abstract][Full Text] [Related]
3. Sickle cell disease in the Kurdish population of northern Iraq.
Al-Allawi NA; Jalal SD; Nerwey FF; Al-Sayan GO; Al-Zebari SS; Alshingaly AA; Markous RD; Jubrael JM; Hamamy H
Hemoglobin; 2012; 36(4):333-42. PubMed ID: 22686351
[TBL] [Abstract][Full Text] [Related]
4. Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest Iran.
Galehdari H; Salehi B; Azmoun S; Keikhaei B; Zandian KM; Pedram M
Hemoglobin; 2010; 34(5):461-8. PubMed ID: 20854120
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey.
Mendilcioglu I; Yakut S; Keser I; Simsek M; Yesilipek A; Bagci G; Luleci G
Hemoglobin; 2011; 35(1):47-55. PubMed ID: 21250881
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.
Cürük MA; Zeren F; Genç A; Ozavci-Aygün S; Kilinç Y; Aksoy K
Hemoglobin; 2008; 32(6):525-30. PubMed ID: 19065329
[TBL] [Abstract][Full Text] [Related]
7. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
Murad H; Moassas F; Jarjour R; Mukhalalaty Y; Al-Achkar W
Hemoglobin; 2014; 38(6):390-3. PubMed ID: 25405916
[TBL] [Abstract][Full Text] [Related]
8. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
Darwish HM; El-Khatib FF; Ayesh S
Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
[TBL] [Abstract][Full Text] [Related]
9. Hb S/
Belisário AR; Carneiro-Proietti AB; Sabino EC; Araújo A; Loureiro P; Máximo C; Flor-Park MV; Rodrigues DDOW; Ozahata MC; McClure C; Mota RA; Gomes Moura IC; Custer B; Kelly S;
Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
[TBL] [Abstract][Full Text] [Related]
10. Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya.
Keser I; Sanlioglu AD; Manguoglu E; Guzeloglu Kayisli O; Nal N; Sargin F; Yesilipek A; Simsek M; Mendilcioglu I; Canatan D; Luleci G
Acta Haematol; 2004; 111(4):205-10. PubMed ID: 15153712
[TBL] [Abstract][Full Text] [Related]
11. Molecular basis of β-thalassemia in the United Arab Emirates.
Baysal E
Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of beta-thalassemia mutations in Guadeloupe.
Romana M; Keclard L; Guillemin G; Lavocat E; Saint-Martin C; Berchel C; Mérault G
Am J Hematol; 1996 Dec; 53(4):228-33. PubMed ID: 8948659
[TBL] [Abstract][Full Text] [Related]
13. [Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
Fattoum S
Tunis Med; 2006 Nov; 84(11):687-96. PubMed ID: 17294892
[TBL] [Abstract][Full Text] [Related]
14. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
Daniel Y; Hill K; Inusa B; Thein SL; Howard J
Hemoglobin; 2011; 35(4):406-10. PubMed ID: 21797706
[TBL] [Abstract][Full Text] [Related]
15. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
Yuzbasioglu Ariyurek S; Yildiz SM; Yalin AE; Guzelgul F; Aksoy K
Hemoglobin; 2016 Jun; 40(3):168-72. PubMed ID: 26984585
[TBL] [Abstract][Full Text] [Related]
16. THE Hb S/beta+ -thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele.
Schmugge M; Waye JS; Basran RK; Zurbriggen K; Frischknecht H
Hemoglobin; 2008; 32(3):303-7. PubMed ID: 18473247
[TBL] [Abstract][Full Text] [Related]
17. High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).
Millimono TS; Loua KM; Rath SL; Relvas L; Bento C; Diakite M; Jarvis M; Daries N; Ribeiro LM; Manco L; Kaeda JS
Hemoglobin; 2012; 36(1):25-37. PubMed ID: 21929367
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.
Al-Sultan A; Phanasgaonkar S; Suliman A; Al-Baqushi M; Nasrullah Z; Al-Ali A
Hemoglobin; 2011; 35(2):125-34. PubMed ID: 21417569
[TBL] [Abstract][Full Text] [Related]
19. Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-thalassemia codon 17 (A>T) in a Thai patient.
Pornprasert S; Panyasai S; Kongthai K; Treesuwan K
Hemoglobin; 2012; 36(3):265-9. PubMed ID: 22471390
[TBL] [Abstract][Full Text] [Related]
20. Beta zero and beta+ thalassemia genes in northern Greece.
Koliakos GG; Dimitriadou-Vaphiadou A; Christakis J; Trakatellis A
Gene Geogr; 1991; 5(1-2):55-60. PubMed ID: 1820156
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
