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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]  

  • 3. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN; Scholtz CL; Hoogendijk CF; Cawood EJ; Kotze MJ
    Hum Genet; 1998 Jan; 102(1):127. PubMed ID: 9490291
    [No Abstract]   [Full Text] [Related]  

  • 4. Clinical haemochromatosis in HFE mutation carriers.
    Poullis A; Moodie SJ; Maxwell JD
    Lancet; 2002 Aug; 360(9330):411-2; author reply 413-4. PubMed ID: 12241803
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM.
    Dubois-Laforgue D; Caillat-Zucman S; Djilali-Saiah I; Larger E; Mercadier A; Boitard C; Bach JF; Timsit J
    Diabetes Care; 1998 Aug; 21(8):1371-2. PubMed ID: 9702455
    [No Abstract]   [Full Text] [Related]  

  • 6. Haemochromatosis, HFE and genetic complexity.
    Risch N
    Nat Genet; 1997 Dec; 17(4):375-6. PubMed ID: 9398831
    [No Abstract]   [Full Text] [Related]  

  • 7. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A; Bortoluzzi L; Jansen S; Fehr J
    Schweiz Med Wochenschr; 2000 Aug; 130(31-32):1112-9. PubMed ID: 11008304
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations.
    Beutler E
    Lancet; 1997 Feb; 349(9048):296-7. PubMed ID: 9024367
    [No Abstract]   [Full Text] [Related]  

  • 9. Haemochromatosis and HLA-H.
    Jouanolle AM; Gandon G; Jézéquel P; Blayau M; Campion ML; Yaouanq J; Mosser J; Fergelot P; Chauvel B; Bouric P; Carn G; Andrieux N; Gicquel I; Le Gall JY; David V
    Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
    [No Abstract]   [Full Text] [Related]  

  • 10. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R; Fagan E; Payne SJ
    Hum Mutat; 2000 Jan; 15(1):120. PubMed ID: 10612845
    [No Abstract]   [Full Text] [Related]  

  • 11. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Burggraf S; Olgemöller B
    Dtsch Med Wochenschr; 2000 Nov; 125(44):1346; author reply 1347. PubMed ID: 11109419
    [No Abstract]   [Full Text] [Related]  

  • 12. Differential HFE allele expression in hemochromatosis heterozygotes.
    Bergamaschi G; Rolandi V; Cazzola M
    Gastroenterology; 2001 Apr; 120(5):1308-9. PubMed ID: 11288747
    [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]  

  • 16. Differential HFE allele expression in hemochromatosis heterozygotes.
    Bayley JP; Verweij CL
    Gastroenterology; 2002 Aug; 123(2):652-3; author reply 653. PubMed ID: 12145827
    [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]
    of 8.