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.
47 related articles for article (PubMed ID: 8316912)
1. 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]
2. High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa. de Villiers JN; Hillerman R; de Jong G; Langenhoven E; Rossouw H; Marx MP; Kotze MJ S Afr Med J; 1999 Mar; 89(3):279-82. PubMed ID: 10226674 [TBL] [Abstract][Full Text] [Related]
3. Hereditary haemochromatosis should be more widely known about. Rosenberg W; Howell M; Roderick P; Eccles D; Day I BMJ; 1999 May; 318(7196):1486-7. PubMed ID: 10346785 [No Abstract] [Full Text] [Related]
4. Population genetic screening for hereditary haemochromatosis. Gertig DM; Hopper JL; Allen KJ Med J Aust; 2003 Nov; 179(10):517-8. PubMed ID: 14609411 [No Abstract] [Full Text] [Related]
5. Iron and ischemic heart disease in the African setting. Walker AR; Walker BF Arch Intern Med; 2000 Jan; 160(2):241-2. PubMed ID: 10647764 [No Abstract] [Full Text] [Related]
6. Hereditary hemochromatosis: a case study and review. Laudicina RJ; Legrys VA Clin Lab Sci; 2001; 14(3):196-208; quiz 220-2. PubMed ID: 11517631 [TBL] [Abstract][Full Text] [Related]
8. [Hereditary hemochromatosis: considerations and proposals]. del Castillo Rueda A; de Portugal Alvarez J Med Clin (Barc); 2002 Oct; 119(11):436-7. PubMed ID: 12381283 [No Abstract] [Full Text] [Related]
9. Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction? Majore S; Ricerca BM; Radio FC; Binni F; Cosentino I; Gallusi G; De Bernardo C; Morrone A; Grammatico P Blood Cells Mol Dis; 2013 Jan; 50(1):31-2. PubMed ID: 22981443 [No Abstract] [Full Text] [Related]
10. Haemochromatosis: where are all the patients? Ho GT; Stanley AJ Scott Med J; 2001 Aug; 46(4):99-100. PubMed ID: 11676045 [No Abstract] [Full Text] [Related]
11. [The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis]. Fábrega E; Castro B; Sánchez-Castro L; Benito A; Fernández-Luna JL; Pons-Romero F Med Clin (Barc); 1999 Apr; 112(12):451-3. PubMed ID: 10320958 [TBL] [Abstract][Full Text] [Related]
12. [Hereditary hemochromatosis. 3 families with high occurrence of diseases in a coastal county]. Pedersen K; Følling I; Lamvik J; Hallan H; Bratlie A Tidsskr Nor Laegeforen; 1985 Aug; 105(22):1385-8. PubMed ID: 4049332 [No Abstract] [Full Text] [Related]
14. [Elevated serum ferritin and hemochromatosis in general practice]. Mouland G; Bratland B; Hornnes MB; Asser HP; Lier J; Reiso H; Rygh E Tidsskr Nor Laegeforen; 2005 Jan; 125(1):20-2. PubMed ID: 15643457 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. Prevalence of genetic haemochromatosis in diabetic patients. Lancet; 1989 Oct; 2(8668):925. PubMed ID: 2571849 [No Abstract] [Full Text] [Related]
17. High prevalence but low pathogenicity of hepatitis G virus infection in Italian patients with genetic haemochromatosis. De Filippi F; Fraquelli M; Conte D; Soffredini R; Prati D; Ronchi G; Zanella A; Del Ninno E; Colombo M Ital J Gastroenterol Hepatol; 1998 Oct; 30(5):529-33. PubMed ID: 9836112 [TBL] [Abstract][Full Text] [Related]
19. Hereditary haemochromatosis: to screen or not to screen? Olynyk JK; Trinder D; Milward E J Hepatol; 2005 Jul; 43(1):9-10. PubMed ID: 15923055 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]