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.
126 related articles for article (PubMed ID: 16433696)
1. Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosity. Matas M; Guix P; Castro JA; Parera M; Ramon MM; Obrador A; Picornell A Clin Genet; 2006 Feb; 69(2):155-62. PubMed ID: 16433696 [TBL] [Abstract][Full Text] [Related]
2. Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: a change of concept required. Reish O; Shefer-Kaufmann N; Shimshoni DC; Renbaum P; Orr-Urtreger A; Steiner H; Rapoport M; Levy-Lahad E; Altarescu G Genet Med; 2010 Feb; 12(2):122-5. PubMed ID: 20084012 [TBL] [Abstract][Full Text] [Related]
3. Distribution of HFE C282Y and H63D mutations in the Balearic Islands (NE Spain). Guix P; Picornell A; Parera M; Galmes A; Obrador A; Ramon MM; Castro JA Clin Genet; 2002 Jan; 61(1):43-8. PubMed ID: 11903355 [TBL] [Abstract][Full Text] [Related]
4. 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 [TBL] [Abstract][Full Text] [Related]
5. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis. Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390 [TBL] [Abstract][Full Text] [Related]
6. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis. Milić S; Ristić S; Starčević-Čizmarević N; Brajenović-Milić B; Crnić-Martinović M; Kapović M; Peterlin B; Štimac D Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608 [TBL] [Abstract][Full Text] [Related]
7. 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 [TBL] [Abstract][Full Text] [Related]
8. Prevalence of hemochromatosis gene (HFE) mutations in Greece. Papazoglou D; Exiara T; Speletas M; Panagopoulos I; Maltezos E Acta Haematol; 2003; 109(3):137-40. PubMed ID: 12714823 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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 [TBL] [Abstract][Full Text] [Related]
11. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic. Cimburova M; Putova I; Provaznikova H; Horak J Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978 [TBL] [Abstract][Full Text] [Related]
12. 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; 8(3):263-7. PubMed ID: 15727249 [TBL] [Abstract][Full Text] [Related]
13. Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina. Terzić R; Sehić A; Teran N; Terzić I; Peterlin B Coll Antropol; 2006 Sep; 30(3):555-7. PubMed ID: 17058523 [TBL] [Abstract][Full Text] [Related]
14. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes. Raddatz D; Legler T; Lynen R; Addicks N; Ramadori G Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375 [TBL] [Abstract][Full Text] [Related]
15. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation. Velati C; Marlianici E; Rigamonti D; Barillari G; Chiavilli F; Fugiani P; Garozzo G; Lancieri M; Rinaldi S; Testa D; Sampietro M; Tavazzi D; Delbini P; Fargion S; Fiorelli G Hematol J; 2003; 4(6):436-40. PubMed ID: 14671617 [TBL] [Abstract][Full Text] [Related]
16. Prevalence of HFE mutations in California newborns. Hoppe C; Watson RM; Long CM; Lorey F; Robles L; Klitz W; Styles L; Vichinsky E Pediatr Hematol Oncol; 2006 Sep; 23(6):507-16. PubMed ID: 16849282 [TBL] [Abstract][Full Text] [Related]
17. Prevalence of common HFE and SERPINA1 mutations in patients with hepatocellular carcinoma in a Moroccan population. Ezzikouri S; El Feydi AE; El Kihal L; Afifi R; Benazzouz M; Hassar M; Chafik A; Pineau P; Benjelloun S Arch Med Res; 2008 Feb; 39(2):236-41. PubMed ID: 18164971 [TBL] [Abstract][Full Text] [Related]
18. Frequency and spectrum of hemochromatosis mutations in Tunisia. Zorai A; Harteveld CL; Rachdi R; Dellagi K; Abbes S; Delbini P; Giordano PC Hematol J; 2003; 4(6):433-5. PubMed ID: 14671616 [TBL] [Abstract][Full Text] [Related]
19. Frequency of the hemochromatosis C282Y and H63D mutations in a Polish population of Slavic origin. Moczulski DK; Grzeszczak W; Gawlik B Med Sci Monit; 2001; 7(3):441-3. PubMed ID: 11386022 [TBL] [Abstract][Full Text] [Related]
20. [Molecular genetic diagnostics and screening of hereditary hemochromatosis]. Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]