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26. [Hemochromatosis: the importance of mutation screening in the family]. ter Braak N; Erdkamp FL; van Deursen CT Ned Tijdschr Geneeskd; 2009 Apr; 153(16):765-7. PubMed ID: 19469149 [No Abstract] [Full Text] [Related]
28. Hereditary haemochromatosis: to screen or not. Conditions for screening are not yet fulfilled. Haddow JE; Bradley LA BMJ; 1999 Aug; 319(7209):531-2. PubMed ID: 10463879 [No Abstract] [Full Text] [Related]
30. HFE Gene Mutations and Iron Status in 100 Healthy Polish Children. Kaczorowska-Hac B; Luszczyk M; Antosiewicz J; Ziolkowski W; Adamkiewicz-Drozynska E; Mysliwiec M; Milosz E; Kaczor JJ J Pediatr Hematol Oncol; 2017 Jul; 39(5):e240-e243. PubMed ID: 28406842 [TBL] [Abstract][Full Text] [Related]
31. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible. Delatycki MB; Wolthuizen M; Collins V; Varley E; Craven J; Allen KJ; Gurrin LC; Aitken M; Trembath MK; Bond L; Wilson GR; Stephenson SE; Macciocca I; Hickerton C; Lockhart PJ; Metcalfe SA Eur J Hum Genet; 2012 May; 20(5):505-9. PubMed ID: 22234159 [TBL] [Abstract][Full Text] [Related]
32. Iron storage disease: facts, fiction and progress. Beutler E Blood Cells Mol Dis; 2007; 39(2):140-7. PubMed ID: 17540589 [TBL] [Abstract][Full Text] [Related]
33. Heteroduplex analysis for the three common HFE variants: methodology, reliability and analysis of over 5000 requests for testing. Kingston J; Bowen D; Sweeney M; Lawless S; Jackson H; Worwood M J Clin Pathol; 2007 Nov; 60(11):1244-8. PubMed ID: 17079357 [TBL] [Abstract][Full Text] [Related]
34. Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients. McCune CA; Ravine D; Carter K; Jackson HA; Hutton D; Hedderich J; Krawczak M; Worwood M Gut; 2006 Apr; 55(4):554-62. PubMed ID: 16174659 [TBL] [Abstract][Full Text] [Related]
35. Should asymptomatic haemochromatosis be treated? Alternative strategies to appropriate diagnosis need testing. Emery J; Rose P BMJ; 2000 Oct; 321(7266):955-6. PubMed ID: 11030697 [No Abstract] [Full Text] [Related]
36. Deaths attributed to haemochromatosis are rare in Britain. Willis G; Fellows IW; Wimperis JZ BMJ; 2000 Apr; 320(7242):1146. PubMed ID: 10775237 [No Abstract] [Full Text] [Related]
37. Screening for hereditary haemochromatosis should be implemented now. Allen K; Williamson R BMJ; 2000 Jan; 320(7228):183-4. PubMed ID: 10634748 [No Abstract] [Full Text] [Related]
38. Hereditary haemochromatosis - diagnosis and management. Allen K Aust Fam Physician; 2010 Dec; 39(12):938-41. PubMed ID: 21301675 [TBL] [Abstract][Full Text] [Related]
39. Should we genetically test everyone for haemochromatosis? Allen K; Williamson R J Med Ethics; 1999 Apr; 25(2):209-14. PubMed ID: 10226930 [TBL] [Abstract][Full Text] [Related]