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5. Hereditary hyperferritinaemia-cataract syndrome and differential diagnosis of hereditary haemochromatosis. Sanders SJ; Suri M; Ross I Postgrad Med J; 2003 Oct; 79(936):600-1. PubMed ID: 14612607 [TBL] [Abstract][Full Text] [Related]
6. A systematic review of the clinical validity and clinical utility of DNA testing for hereditary haemochromatosis type 1 in at-risk populations. Bryant J; Cooper K; Picot J; Clegg A; Roderick P; Rosenberg W; Patch C J Med Genet; 2008 Aug; 45(8):513-8. PubMed ID: 18310265 [TBL] [Abstract][Full Text] [Related]
7. Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis. Baty D; Terron Kwiatkowski A; Mechan D; Harris A; Pippard MJ; Goudie D J Clin Pathol; 1998 Jan; 51(1):73-4. PubMed ID: 9577377 [TBL] [Abstract][Full Text] [Related]
10. [Importance of hereditary haemochromatosis in the care of diabetes mellitus]. Wittmann I; Wagner L; Markó L; Tamaskó M; Laczy B; Márton M; Cseh J; Melegh B Orv Hetil; 2007 Jan; 148(3):111-5. PubMed ID: 17289614 [TBL] [Abstract][Full Text] [Related]
11. Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. Nielsen JE; Jensen LN; Krabbe K J Neurol Neurosurg Psychiatry; 1995 Sep; 59(3):318-21. PubMed ID: 7673967 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Hereditary haemochromatosis--a South African perspective. Bothwell TH; Hitzeroth HW S Afr Med J; 1993 Apr; 83(4):236-7. PubMed ID: 8316912 [No Abstract] [Full Text] [Related]
16. [Hereditary hemochromatosis. Genetic findings result in new therapeutic possibilities]. Beckman LE; Beckman L Lakartidningen; 1997 Oct; 94(44):3961-2. PubMed ID: 9411163 [TBL] [Abstract][Full Text] [Related]
17. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy. De Marco F; Liguori R; Giardina MG; D'Armiento M; Angelucci E; Lucariello A; Morante R; Cimino L; Galeota-Lanza A; Tarantino G; Ascione A; Budillon G; Vecchione R; Martinelli R; Matarazzo M; De Simone V Clin Chem Lab Med; 2004 Jan; 42(1):17-24. PubMed ID: 15061375 [TBL] [Abstract][Full Text] [Related]
18. Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene. Aslam S; Standen GR Postgrad Med J; 1997 Sep; 73(863):573-4. PubMed ID: 9373599 [TBL] [Abstract][Full Text] [Related]