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.
155 related articles for article (PubMed ID: 9726605)
1. Hereditary haemochromatosis mutations (HFE) in patients with Type II diabetes mellitus. Braun J; Donner H; Plock K; Rau H; Usadel KH; Badenhoop K Diabetologia; 1998 Aug; 41(8):983-4. PubMed ID: 9726605 [No Abstract] [Full Text] [Related]
2. Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study. Salonen JT; Tuomainen TP; Kontula K BMJ; 2000 Jun; 320(7251):1706-7. PubMed ID: 10864547 [No Abstract] [Full Text] [Related]
13. Idiopathic hemochromatosis with the mutation of Ala176Val heterozygous for HFE gene. Imanishi H; Liu W; Cheng J; Ikeda N; Amuro Y; Hada T Intern Med; 2001 Jun; 40(6):479-83. PubMed ID: 11446670 [TBL] [Abstract][Full Text] [Related]
14. Haemochromatosis: diagnosis and management after the cloning of the HFE gene. Powell LW; Bassett ML Aust N Z J Med; 1998 Apr; 28(2):159-63. PubMed ID: 9612522 [No Abstract] [Full Text] [Related]
15. Diagnosis and management of haemochromatosis since the discovery of the HFE gene: a European experience. Br J Haematol; 2000 Jan; 108(1):31-9. PubMed ID: 10651721 [No Abstract] [Full Text] [Related]
17. High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation. Tordai A; Andrikovics H; Kalmár L; Rajczy K; Pénzes M; Sarkadi B; Klein I; Váradi A J Med Genet; 1998 Oct; 35(10):878-9. PubMed ID: 9783719 [No Abstract] [Full Text] [Related]
18. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis. Jeffrey GP; Chakrabarti S; Hegele RA; Adams PC Nat Genet; 1999 Aug; 22(4):325-6. PubMed ID: 10431233 [No Abstract] [Full Text] [Related]
19. Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study. Halsall DJ; McFarlane I; Luan J; Cox TM; Wareham NJ Hum Mol Genet; 2003 Jun; 12(12):1361-5. PubMed ID: 12783844 [TBL] [Abstract][Full Text] [Related]
20. Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload. Townsend A; Drakesmith H Lancet; 2002 Mar; 359(9308):786-90. PubMed ID: 11888608 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]