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.
66 related articles for article (PubMed ID: 12401773)
1. The role of hemochromatosis C282Y and H63D gene mutations in type 2 diabetes: findings from the Rotterdam Study and meta-analysis. Njajou OT; Alizadeh BZ; Vaessen N; Vergeer J; Houwing-Duistermaat J; Hofman A; Pols HA; Van Duijn CM Diabetes Care; 2002 Nov; 25(11):2112-3. PubMed ID: 12401773 [No Abstract] [Full Text] [Related]
2. 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]
3. [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]
4. C282Y and H63D mutations of the hemochromatosis candidate gene in type 2 diabetes. Fernandez-Real JM; Vendrell J; Baiget M; Gimferrer E; Ricart W Diabetes Care; 1999 Mar; 22(3):525-6. PubMed ID: 10097942 [No Abstract] [Full Text] [Related]
5. Patients with type 2 diabetes have a high frequency of the C282Y mutation of the hemochromatosis gene. Kwan T; Leber B; Ahuja S; Carter R; Gerstein HC Clin Invest Med; 1998 Dec; 21(6):251-7. PubMed ID: 9885759 [TBL] [Abstract][Full Text] [Related]
6. Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls. Ellervik C; Birgens H; Tybjaerg-Hansen A; Nordestgaard BG Hepatology; 2007 Oct; 46(4):1071-80. PubMed ID: 17828789 [TBL] [Abstract][Full Text] [Related]
7. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis. Walsh A; Dixon JL; Ramm GA; Hewett DG; Lincoln DJ; Anderson GJ; Subramaniam VN; Dodemaide J; Cavanaugh JA; Bassett ML; Powell LW Clin Gastroenterol Hepatol; 2006 Nov; 4(11):1403-10. PubMed ID: 16979952 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
11. 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]
12. Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C. Sumner K; Hubley L; Pont-Kingdon G; Mitchell S; Wayman T; Wilson A; Meadows C; Elenitoba-Johnson K; Pattison D; Dobrowolski S; Best H; Lyon E Genet Test Mol Biomarkers; 2012 Jul; 16(7):656-60. PubMed ID: 22364140 [TBL] [Abstract][Full Text] [Related]
13. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study. Adams PC; Pankow JS; Barton JC; Acton RT; Leiendecker-Foster C; McLaren GD; Speechley M; Eckfeldt JH Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565 [TBL] [Abstract][Full Text] [Related]
14. A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population. Małecki MT; Klupa T; Waluś M; Czogała W; Greenlaw P; Sieradzki J Med Sci Monit; 2003 Feb; 9(2):BR91-5. PubMed ID: 12601293 [TBL] [Abstract][Full Text] [Related]
15. Lack of association of C282Y and H63D mutations in the hemochromatosis (HFE) gene with diabetes mellitus type 2 in a case-control study of women in Brazil. Gomes KB; Carvalho MG; Coelho FF; Rodrigues IF; Soares AL; Guimarães DA; Fernandes AP Genet Mol Res; 2009 Oct; 8(4):1285-91. PubMed ID: 19876870 [TBL] [Abstract][Full Text] [Related]
16. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population]. Larsen LE; Ellervik C; Appleyard M; Nordestgaard BG; Birgens H; Tybjaerg-Hansen A Ugeskr Laeger; 2002 Sep; 164(39):4545-7. PubMed ID: 12380399 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genetics of hemochromatosis. Cullen LM; Anderson GJ; Ramm GA; Jazwinska EC; Powell LW Annu Rev Med; 1999; 50():87-98. PubMed ID: 10073265 [TBL] [Abstract][Full Text] [Related]
19. The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading. Livesey KJ; Wimhurst VL; Carter K; Worwood M; Cadet E; Rochette J; Roberts AG; Pointon JJ; Merryweather-Clarke AT; Bassett ML; Jouanolle AM; Mosser A; David V; Poulton J; Robson KJ J Med Genet; 2004 Jan; 41(1):6-10. PubMed ID: 14729817 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]