133 related articles for article (PubMed ID: 17303462)
1. [HFE gene mutations in Tunisian major beta-Thalassemia and iron overload].
Mellouli F; El Borgi W; Kaabi H; Ben Hassen E; Sassi R; Hmida H; Cherif G; Maamar M; Zouari B; Boukef K; Bejaoui M; Hmida S
Transfus Clin Biol; 2006 Dec; 13(6):353-7. PubMed ID: 17303462
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.
Garewal G; Das R; Ahluwalia J; Marwaha RK
Eur J Haematol; 2005 Apr; 74(4):333-6. PubMed ID: 15777346
[TBL] [Abstract][Full Text] [Related]
3. The influence of hemochromatosis mutations on iron overload of thalassemia major.
Longo F; Zecchina G; Sbaiz L; Fischer R; Piga A; Camaschella C
Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452
[TBL] [Abstract][Full Text] [Related]
4. Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan.
Sharif Y; Irshad S; Tariq A; Rasheed S; Tariq MH
Saudi Med J; 2019 Sep; 40(9):887-892. PubMed ID: 31522215
[TBL] [Abstract][Full Text] [Related]
5. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
Melis MA; Cau M; Deidda F; Barella S; Cao A; Galanello R
Haematologica; 2002 Mar; 87(3):242-5. PubMed ID: 11869934
[TBL] [Abstract][Full Text] [Related]
6. Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients.
Rahmani R; Naseri P; Safaroghli-Azar A; Tarighi S; Hosseini T; Hojjati MT
Transfus Clin Biol; 2019 Nov; 26(4):249-252. PubMed ID: 31679808
[TBL] [Abstract][Full Text] [Related]
7. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
[TBL] [Abstract][Full Text] [Related]
8. The effect of HFE polymorphisms on cardiac iron overload in patients with beta-thalassemia major.
Turedi A; Oymak Y; Meşe T; Yaman Y; Bayraktaroglu S; Alpman A; Ozkinay F; Aydınok Y; Vergin C
Pediatr Hematol Oncol; 2013 Nov; 30(8):755-60. PubMed ID: 24087894
[TBL] [Abstract][Full Text] [Related]
9. Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.
Viprakasit V; Vathesathokit P; Chinchang W; Tachavanich K; Pung-Amritt P; Wimhurst VL; Yenchitsomanus PT; Merryweather-Clarke AT; Tanphaichitr VS
Eur J Haematol; 2004 Jul; 73(1):43-9. PubMed ID: 15182337
[TBL] [Abstract][Full Text] [Related]
10. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
Sassi R; Hmida S; Kaabi H; Hajjej A; Abid A; Abdelkefi S; Yacoub S; Maamar M; Mojaat N; Ben Hamed L; Bellali H; Dridi A; Jridi A; Midouni B; Boukef MK
Ann Genet; 2004; 47(4):325-30. PubMed ID: 15581829
[TBL] [Abstract][Full Text] [Related]
11. Frequency of HFE gene mutations in Iranian beta-thalassaemia minor patients.
Jazayeri M; Bakayev V; Adibi P; Haghighi Rad F; Zakeri H; Kalantar E; Zali MR
Eur J Haematol; 2003 Dec; 71(6):408-11. PubMed ID: 14703689
[TBL] [Abstract][Full Text] [Related]
12. Role of HFE gene mutations on developing iron overload in beta-thalassaemia carriers in Egypt.
Madani HA; Afify RA; Abd El-Aal AA; Salama N; Ramy N
East Mediterr Health J; 2011 Jun; 17(6):546-51. PubMed ID: 21796974
[TBL] [Abstract][Full Text] [Related]
13. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City.
Baptista-González HA; Rosenfeld-Mann F; Trueba-Gómez R; Bermejo-Martínez L; Méndez-Sánchez N
Ann Hepatol; 2007; 6(1):55-60. PubMed ID: 17297430
[TBL] [Abstract][Full Text] [Related]
14. The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
Martins R; Picanço I; Fonseca A; Ferreira L; Rodrigues O; Coelho M; Seixas T; Miranda A; Nunes B; Costa L; Romão L; Faustino P
J Hum Genet; 2004; 49(12):651-655. PubMed ID: 15538648
[TBL] [Abstract][Full Text] [Related]
15. Status of HFE mutation in thalassemia syndromes in north India.
Agarwal S; Tewari D; Arya V; Moorchung N; Tripathi R; Chaudhuri G; Pradhan M
Ann Hematol; 2007 Jul; 86(7):483-5. PubMed ID: 17401564
[TBL] [Abstract][Full Text] [Related]
16. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.
Floreani A; Rosa Rizzotto E; Basso D; Navaglia F; Zaninotto M; Petridis I; DI Andrea O; Testa R; Marra M; Baldo V; Chiaramonte M
Aliment Pharmacol Ther; 2007 Aug; 26(4):577-86. PubMed ID: 17661761
[TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
Vizzi E; Loureiro CL; Gerder M; de las Nieves Garcia-Casal M; Rodríguez-Larralde A; Gerace L; Ludert JE; Liprandi F; Pujol FH
Ann Hematol; 2005 Nov; 84(12):802-6. PubMed ID: 15995871
[TBL] [Abstract][Full Text] [Related]
18. HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions.
Sharma V; Panigrahi I; Dutta P; Tyagi S; Choudhry VP; Saxena R
Indian J Pathol Microbiol; 2007 Jan; 50(1):82-5. PubMed ID: 17474269
[TBL] [Abstract][Full Text] [Related]
19. H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers.
Yamsri S; Sanchaisuriya K; Fucharoen S; Fucharoen G; Jetsrisuparb A; Wiangnon S; Changtrakul Y; Sanchaisuriya P
Acta Haematol; 2007; 118(2):99-105. PubMed ID: 17637512
[TBL] [Abstract][Full Text] [Related]
20. The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
Politou M; Kalotychou V; Pissia M; Rombos Y; Sakellaropoulos N; Papanikolaou G
Haematologica; 2004 Apr; 89(4):490-2. PubMed ID: 15075083
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
