These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. 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 Dec; 49(12):651-655. PubMed ID: 15538648 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population. Kucinskas L, Juzenas S, Sventoraityte J, Cedaviciute R, Vitkauskiene A, Kalibatas V, Kondrackiene J, Kupcinskas L. Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086 [Abstract] [Full Text] [Related]
5. Heterozygosity for the H63D mutation in the hereditary hemochromatosis (HFE) gene may lead into severe iron overload in beta-thalassemia minor: observations in a thalassemic kindred. Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Sánchez-Anzaldo J, Ruiz-Delgado GJ, Jiménez-González C, Carrera B. Rev Invest Clin; 2001 Apr; 53(2):117-20. PubMed ID: 11421105 [Abstract] [Full Text] [Related]
6. 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 [Abstract] [Full Text] [Related]
7. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population. Leone PE, Giménez P, Collantes JC, Paz-y-Miño C. Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265 [Abstract] [Full Text] [Related]
8. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania. Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV. J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. [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 [Abstract] [Full Text] [Related]
11. 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 [Abstract] [Full Text] [Related]
12. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population. Lin A, Yan WH, Xu HH, Zhu M, Zhou MY. Tissue Antigens; 2007 Sep; 70(3):252-5. PubMed ID: 17661915 [Abstract] [Full Text] [Related]
13. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls. Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P. Gut; 2002 Nov; 51(5):723-30. PubMed ID: 12377814 [Abstract] [Full Text] [Related]
14. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain. de Diego C, Murga MJ, Martínez-Castro P. Genet Test; 2004 Nov; 8(3):263-7. PubMed ID: 15727249 [Abstract] [Full Text] [Related]
15. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene]. Drastíková M, Beránek M, Hegerová J, Putzová D. Cas Lek Cesk; 2012 Nov; 151(9):428-31. PubMed ID: 23102134 [Abstract] [Full Text] [Related]
16. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal). Spínola C, Brehm A, Spínola H. Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725 [Abstract] [Full Text] [Related]
17. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain. Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M. Genet Test; 2004 Jan; 8(4):407-10. PubMed ID: 15684872 [Abstract] [Full Text] [Related]
18. 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 [Abstract] [Full Text] [Related]
19. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands. Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC. Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317 [Abstract] [Full Text] [Related]
20. Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers. Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K. J Clin Lab Anal; 2017 May; 31(3):. PubMed ID: 27561698 [Abstract] [Full Text] [Related] Page: [Next] [New Search]