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23. Haemochromatosis and the liver. Niederau C; Erhardt A; Häussinger D; Strohmeyer G J Hepatol; 1999; 30 Suppl 1():6-11. PubMed ID: 10370895 [No Abstract] [Full Text] [Related]
24. [The prioritisation of genetic screening with primary haemochromatosis as an example]. de Craen AJ; van Aken MO; Westendorp RG Ned Tijdschr Geneeskd; 2003 Jul; 147(30):1442-5. PubMed ID: 12908344 [TBL] [Abstract][Full Text] [Related]
25. Hereditary haemochromatosis - diagnosis and management. Allen K Aust Fam Physician; 2010 Dec; 39(12):938-41. PubMed ID: 21301675 [TBL] [Abstract][Full Text] [Related]
26. Hereditary haemochromatosis: never seen a case? Emery J; Rose P Br J Gen Pract; 2001 May; 51(466):347-8. PubMed ID: 11360695 [No Abstract] [Full Text] [Related]
27. Review article: the modern diagnosis and management of haemochromatosis. Adams PC Aliment Pharmacol Ther; 2006 Jun; 23(12):1681-91. PubMed ID: 16817911 [TBL] [Abstract][Full Text] [Related]
28. Cost-Effectiveness of Different Population Screening Strategies for Hereditary Haemochromatosis in Australia. de Graaff B; Neil A; Si L; Yee KC; Sanderson K; Gurrin L; Palmer AJ Appl Health Econ Health Policy; 2017 Aug; 15(4):521-534. PubMed ID: 28035629 [TBL] [Abstract][Full Text] [Related]
29. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium. Merryweather-Clarke AT; Pointon JJ; Shearman JD; Robson KJ; Jouanolle AM; Mosser A; David V; Le Gall JY; Halsall DJ; Elsey TS; Kelly A; Cox TM; Clare M; Bomford A; Vandwalle JL; Rochette J; Borot N; Coppin H; Roth MP; Ryan E; Crowe J; Totaro A; Gasparini P; Roetto A; Walker AP Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942 [No Abstract] [Full Text] [Related]
30. Early detection of genetic hemochromatosis: should all young adults be offered the genetic test? Worwood M Genet Test; 2000; 4(2):219-28. PubMed ID: 10953963 [TBL] [Abstract][Full Text] [Related]
31. [Should one screen systematically for genetic haemochromatosis?]. Le Gall JY Presse Med; 2003 Oct; 32(34):1588-90. PubMed ID: 14576578 [No Abstract] [Full Text] [Related]
32. Role of early case detection by screening relatives of patients with HFE-associated hereditary haemochromatosis. Powell LW; Dixon JL; Hewett DG Best Pract Res Clin Haematol; 2005 Jun; 18(2):221-34. PubMed ID: 15737886 [TBL] [Abstract][Full Text] [Related]
34. A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations. Cooper K; Bryant J; Picot J; Clegg A; Roderick PR; Rosenberg WM; Patch C QJM; 2008 Aug; 101(8):631-41. PubMed ID: 18522976 [TBL] [Abstract][Full Text] [Related]
35. Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases? Cadet E; Capron D; Gallet M; Omanga-Léké ML; Boutignon H; Julier C; Robson KJ; Rochette J J Med Genet; 2005 May; 42(5):390-5. PubMed ID: 15863667 [TBL] [Abstract][Full Text] [Related]
36. Costs associated with hereditary haemochromatosis in Australia: a cost-of-illness study. de Graaff B; Neil A; Sanderson K; Yee KC; Palmer AJ Aust Health Rev; 2017 Jul; 41(3):254-267. PubMed ID: 27444148 [TBL] [Abstract][Full Text] [Related]
37. Genetic screening for iron overload: No evidence of discrimination at 1 year. Hall MA; Barton JC; Adams PC; McLaren CE; Reiss JA; Castro O; Ruggiero A; Acton RT; Power TE; Bent TC J Fam Pract; 2007 Oct; 56(10):829-34. PubMed ID: 17908514 [TBL] [Abstract][Full Text] [Related]
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39. [Hereditary hemochromatosis HFE: regulatory and economic aspects of diagnosis and medical management]. Ropert-Bouchet M; Fajardy I; Michel H Ann Biol Clin (Paris); 2012; 70(4):405-11. PubMed ID: 22796612 [TBL] [Abstract][Full Text] [Related]
40. Family screening for genetic haemochromatosis. What is the most effective method of contact? Clayton C; Hall P; Mackinnon M Med J Aust; 1993 Nov; 159(9):614-5. PubMed ID: 8232038 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]