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.
5. Screening for hemochromatosis in asymptomatic subjects with or without a family history. Powell LW; Dixon JL; Ramm GA; Purdie DM; Lincoln DJ; Anderson GJ; Subramaniam VN; Hewett DG; Searle JW; Fletcher LM; Crawford DH; Rodgers H; Allen KJ; Cavanaugh JA; Bassett ML Arch Intern Med; 2006 Feb; 166(3):294-301. PubMed ID: 16476869 [TBL] [Abstract][Full Text] [Related]
6. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants. Pedersen P; Milman N Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930 [TBL] [Abstract][Full Text] [Related]
7. Hereditary hemochromatosis. Walker EM; Wolfe MD; Norton ML; Walker SM; Jones MM Ann Clin Lab Sci; 1998; 28(5):300-12. PubMed ID: 9784832 [TBL] [Abstract][Full Text] [Related]
8. Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools. Delatycki MB; Wolthuizen M; Collins V; Varley E; Craven J; Allen KJ; Aitken MA; Bond L; Lockhart PJ; Wilson GR; Macciocca I; Metcalfe SA Clin Genet; 2010 Mar; 77(3):241-8. PubMed ID: 19930418 [TBL] [Abstract][Full Text] [Related]
10. Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families. Adams PC; Campion ML; Gandon G; LeGall JY; David V; Jouanolle AM Hepatology; 1997 Oct; 26(4):986-90. PubMed ID: 9328324 [TBL] [Abstract][Full Text] [Related]
11. [Iron storage disease]. Horváth G; Dávid K Orv Hetil; 2004 Sep; 145(39):1979-84. PubMed ID: 15553908 [TBL] [Abstract][Full Text] [Related]
12. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation. Shaheen NJ; Bacon BR; Grimm IS Hepatology; 1998 Aug; 28(2):526-9. PubMed ID: 9696020 [TBL] [Abstract][Full Text] [Related]
13. [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis]. Andrikovics H; Klein I; Kalmár L; Bors A; Jermendy G; Petri I; Kalász L; Váradi A; Tordai A Orv Hetil; 1999 Nov; 140(45):2517-22. PubMed ID: 10586619 [TBL] [Abstract][Full Text] [Related]
14. Screening for hemochromatosis: patients with liver disease, families, and populations. Galhenage SP; Viiala CH; Olynyk JK Curr Gastroenterol Rep; 2004 Feb; 6(1):44-51. PubMed ID: 14720453 [TBL] [Abstract][Full Text] [Related]
16. Review article: the screening, diagnosis and optimal management of haemochromatosis. George DK; Powell LW Aliment Pharmacol Ther; 1997 Aug; 11(4):631-9. PubMed ID: 9305470 [TBL] [Abstract][Full Text] [Related]
17. Haemochromatosis: a clinical update for the practising physician. Radford-Smith DE; Powell EE; Powell LW Intern Med J; 2018 May; 48(5):509-516. PubMed ID: 29722188 [TBL] [Abstract][Full Text] [Related]
18. An efficient machine learning-based approach for screening individuals at risk of hereditary haemochromatosis. Martins Conde P; Sauter T; Nguyen TP Sci Rep; 2020 Nov; 10(1):20613. PubMed ID: 33244054 [TBL] [Abstract][Full Text] [Related]
19. The diagnosis and management of hereditary haemochromatosis. Clark P; Britton LJ; Powell LW Clin Biochem Rev; 2010 Feb; 31(1):3-8. PubMed ID: 20179792 [TBL] [Abstract][Full Text] [Related]
20. Public health aspects of genetic screening for hereditary haemochromatosis in Australia. Gertig DM; Fletcher A; Hopper JL Aust N Z J Public Health; 2002 Dec; 26(6):518-24. PubMed ID: 12530795 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]