BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

290 related articles for article (PubMed ID: 11001800)

  • 1. Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?
    Adams PC
    Mol Genet Metab; 2000; 71(1-2):81-6. PubMed ID: 11001800
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD; Flora K; Gross C; Rabkin JM; Corless CL
    Am J Clin Pathol; 1998 May; 109(5):577-84. PubMed ID: 9576576
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A primer for predicting risk of disease in HFE-linked hemochromatosis.
    Adams PC; Walker AP; Acton RT
    Genet Test; 2001; 5(4):311-6. PubMed ID: 11960576
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Update on hereditary hemochromatosis and the HFE gene.
    Brandhagen DJ; Fairbanks VF; Batts KP; Thibodeau SN
    Mayo Clin Proc; 1999 Sep; 74(9):917-21. PubMed ID: 10488796
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.
    Adams PC; Chakrabarti S
    Gastroenterology; 1998 Feb; 114(2):319-23. PubMed ID: 9453492
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.
    McLaren GD; McLaren CE; Adams PC; Barton JC; Reboussin DM; Gordeuk VR; Acton RT; Harris EL; Speechley MR; Sholinsky P; Dawkins FW; Snively BM; Vogt TM; Eckfeldt JH;
    Can J Gastroenterol; 2008 Nov; 22(11):923-30. PubMed ID: 19018338
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Penetrance of the C28Y/C282Y genotype of the HFE gene.
    Asberg A; Hveem K; Kannelønning K; Irgens WØ
    Scand J Gastroenterol; 2007 Sep; 42(9):1073-7. PubMed ID: 17710673
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?
    Ryan E; Byrnes V; Coughlan B; Flanagan AM; Barrett S; O'Keane JC; Crowe J
    Gut; 2002 Jul; 51(1):108-12. PubMed ID: 12077102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis.
    Distante S; Berg JP; Lande K; Haug E; Bell H
    Gut; 2000 Oct; 47(4):575-9. PubMed ID: 10986220
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hemochromatosis in Ireland and HFE.
    Ryan E; O'keane C; Crowe J
    Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary haemochromatosis: diagnosis and management in the gene era.
    Olynyk JK
    Liver; 1999 Apr; 19(2):73-80. PubMed ID: 10220735
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK; Cullen DJ; Aquilia S; Rossi E; Summerville L; Powell LW
    N Engl J Med; 1999 Sep; 341(10):718-24. PubMed ID: 10471457
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The S65C mutation in Spain. Implications for iron overload screening.
    Remacha AF; Barceló MJ; Sardà MP; Blesa I; Altés A; Baiget M
    Haematologica; 2000 Dec; 85(12):1324-5. PubMed ID: 11114141
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis.
    El-Serag HB; Inadomi JM; Kowdley KV
    Ann Intern Med; 2000 Feb; 132(4):261-9. PubMed ID: 10681280
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic hemochromatosis and the HFE gene].
    Moirand R
    Bull Acad Natl Med; 2000; 184(2):325-35; discussion 335-6. PubMed ID: 10989541
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E; Cerani P; Rolandi V; Rovati A; Bergamaschi G
    Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pitfalls in the genetic diagnosis of hereditary hemochromatosis.
    Jeffrey GP; Adams PC
    Genet Test; 2000; 4(2):143-6. PubMed ID: 10953953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Iron in the era of molecular biology].
    Deugnier Y; Moirand R; Brissot P; David V
    Pathol Biol (Paris); 1999 Nov; 47(9):938-44. PubMed ID: 10609274
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.