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 *

29 related articles for article (PubMed ID: 12090054)

  • 1. High headache prevalence among women with hemochromatosis: the Nord-Trøndelag health study.
    Hagen K; Stovner LJ; Asberg A; Thorstensen K; Bjerve KS; Hveem K
    Ann Neurol; 2002 Jun; 51(6):786-9. PubMed ID: 12112089
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Should we support large-scale screening for genetic haemochromatosis in France?].
    Deugnier Y; Le Gall JY
    Bull Acad Natl Med; 2004; 188(2):265-72; discussion 272-3. PubMed ID: 15506717
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Investigation of genetic variants of genes of the hemochromatosis pathway and their role in breast cancer.
    Abraham BK; Justenhoven C; Pesch B; Harth V; Weirich G; Baisch C; Rabstein S; Ko YD; Brüning T; Fischer HP; Haas S; Brod S; Oberkanins C; Hamann U; Brauch H;
    Cancer Epidemiol Biomarkers Prev; 2005 May; 14(5):1102-7. PubMed ID: 15894659
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of C282Y and H63D mutations of the hemochromatosis gene (HFE) in blood donors from Córdoba, Argentina.
    Soria NW; Cossy Isasi S; Chaig MR; Gerez de Burgos NM
    Ann Hematol; 2009 Jan; 88(1):77-9. PubMed ID: 18633618
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Letter regarding article by Ellervik et al, "hereditary hemochromatosis and risk of ischemic heart disease: a prospective study and a case-control study".
    Goland S; Malnick SD
    Circulation; 2006 Jan; 113(1):e10; author reply e10. PubMed ID: 16391159
    [No Abstract]   [Full Text] [Related]  

  • 7. Distribution of the C282Y and H63D polymorphisms in hereditary hemochromatosis patients from the French Basque Country.
    Bauduer F; Scribans C; Degioanni A; Renoux M; Dutour O
    Ann Hematol; 2005 Feb; 84(2):99-102. PubMed ID: 15503019
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel ferroportin mutation in a Canadian family with autosomal dominant hemochromatosis.
    Morris TJ; Litvinova MM; Ralston D; Mattman A; Holmes D; Lockitch G
    Blood Cells Mol Dis; 2005; 35(3):309-14. PubMed ID: 16111902
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hemochromatosis gene mutations and distal adenomatous colorectal polyps.
    McGlynn KA; Sakoda LC; Hu Y; Schoen RE; Bresalier RS; Yeager M; Chanock S; Hayes RB; Buetow KH
    Cancer Epidemiol Biomarkers Prev; 2005 Jan; 14(1):158-63. PubMed ID: 15668490
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.
    Le Gac G; Mons F; Jacolot S; Scotet V; Férec C; Frébourg T
    Br J Haematol; 2004 Jun; 125(5):674-8. PubMed ID: 15147384
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prediction of progression to cirrhosis by a glutathione S-transferase P1 polymorphism in subjects with hereditary hemochromatosis.
    Stickel F; Osterreicher CH; Datz C; Ferenci P; Wölfel M; Norgauer W; Kraus MR; Wrba F; Hellerbrand C; Schuppan D
    Arch Intern Med; 2005 Sep; 165(16):1835-40. PubMed ID: 16157826
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Inheritance of hemochromatosis].
    Hirth L
    Dtsch Med Wochenschr; 1980 Jan; 105(4):115. PubMed ID: 7351192
    [No Abstract]   [Full Text] [Related]  

  • 13. [Hemochromatosis: from phenotype to genotype].
    De Portugal Alvarez J
    An Med Interna; 2002 Apr; 19(4):163-5. PubMed ID: 12090054
    [No Abstract]   [Full Text] [Related]  

  • 14. Screening for hemochromatosis: phenotyping or genotyping or both?
    Tavill AS
    Am J Gastroenterol; 1999 Jun; 94(6):1430-3. PubMed ID: 10364003
    [No Abstract]   [Full Text] [Related]  

  • 15. [Familial survey on a patient with idiopathic hemochromatosis. Therapeutic implications].
    Simon M; Le Mignon L
    Diabete Metab; 1984 Sep; 10(3):223-4. PubMed ID: 6489581
    [No Abstract]   [Full Text] [Related]  

  • 16. The penetrance of hereditary hemochromatosis.
    Waalen J; Nordestgaard BG; Beutler E
    Best Pract Res Clin Haematol; 2005 Jun; 18(2):203-20. PubMed ID: 15737885
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.