BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 19796184)

  • 1. Juvenile hemochromatosis due to homozygosity for the G320V mutation in the HJV gene with fatal outcome.
    Brakensiek K; Fegbeutel C; Mälzer M; Strüber M; Kreipe H; Stuhrmann M
    Clin Genet; 2009 Nov; 76(5):493-5. PubMed ID: 19796184
    [No Abstract]   [Full Text] [Related]  

  • 2. Hemochromatosis and hemojuvelin G320V homozygosity in a Hungarian woman.
    Várkonyi J; Lueff S; Szucs N; Pozsonyi Z; Tóth A; Karádi I; Pietrangelo A
    Acta Haematol; 2010; 123(3):191-3. PubMed ID: 20234129
    [No Abstract]   [Full Text] [Related]  

  • 3. Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.
    Militaru MS; Popp RA; Trifa AP
    J Gastrointestin Liver Dis; 2010 Jun; 19(2):191-3. PubMed ID: 20593054
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HFE gene and hemochromatosis.
    Anderson GJ; Ramm GA; Subramaniam VN; Powell LW
    J Gastroenterol Hepatol; 2004 Jun; 19(6):712. PubMed ID: 15151632
    [No Abstract]   [Full Text] [Related]  

  • 5. Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl.
    Aguilar-Martinez P; Lok CY; Cunat S; Cadet E; Robson K; Rochette J
    Haematologica; 2007 Mar; 92(3):421-2. PubMed ID: 17339196
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Natural history of hemochromatosis.
    Beutler E
    Mayo Clin Proc; 2004 Mar; 79(3):305-6. PubMed ID: 15008601
    [No Abstract]   [Full Text] [Related]  

  • 7. Clinical expression of hemochromatosis gene (HFE) variants.
    Ayonrinde OT; Olynyk JK
    Hepatology; 2007 Oct; 46(4):960-2. PubMed ID: 17894321
    [No Abstract]   [Full Text] [Related]  

  • 8. Hemochromatosis, HFE C282Y homozygosity, and polycystic ovary syndrome: report of two cases and possible effects of androgens and hepcidin.
    Barton JC; Barton JC
    Acta Haematol; 2011; 126(3):138-40. PubMed ID: 21701160
    [No Abstract]   [Full Text] [Related]  

  • 9. Homozygosity for a novel nonsense mutation (G66X) of the HJV gene causes severe juvenile hemochromatosis with fatal cardiomyopathy.
    Jánosi A; Andrikovics H; Vas K; Bors A; Hubay M; Sápi Z; Tordai A
    Blood; 2005 Jan; 105(1):432. PubMed ID: 15611318
    [No Abstract]   [Full Text] [Related]  

  • 10. [Liver pathology in patients with primary hemochromatosis--homozygous carriers of C282Y mutation ].
    Smirnov OA; Shneĭder OV; Radchenko VG; Nilova VK; Okon EE; Kudriavtsev BN; Saburova GS; Mitrofanov NA; Stanzhevskiĭ AA
    Arkh Patol; 2003; 65(4):51-5. PubMed ID: 14518196
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC; Wiener HW; Acton RT; Go RC
    Blood Cells Mol Dis; 2005; 34(1):38-47. PubMed ID: 15607698
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygous deletion of HFE is the common cause of hemochromatosis in Sardinia.
    Le Gac G; Congiu R; Gourlaouen I; Cau M; Férec C; Melis MA
    Haematologica; 2010 Apr; 95(4):685-7. PubMed ID: 20007136
    [No Abstract]   [Full Text] [Related]  

  • 13. Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians.
    Coppin H; Bensaid M; Fruchon S; Borot N; Blanché H; Roth MP
    BMJ; 2003 Jul; 327(7407):132-3. PubMed ID: 12869454
    [No Abstract]   [Full Text] [Related]  

  • 14. New HJV mutation in a patient with hyperferritinemia and H63D homozygosity for the HFE gene.
    de Diego C; Opazo S; Sánchez-Castaño A; Martínez-Castro P
    Int J Hematol; 2007 Nov; 86(4):379-80. PubMed ID: 18055350
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. [Mutation analysis of the pathogenic gene in a Chinese family with hereditary hemochromatosis].
    Yuanfeng L; Hongxing Z; Haitao Z; Xiaobo P; Lili B; Fuchu H; Zewu Q; Gangqiao Z
    Yi Chuan; 2014 Nov; 36(11):1152-8. PubMed ID: 25567873
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tauroursodeoxycholic acid: relieving the pathogenesis of HFE C282Y hereditary hemochromatosis.
    Lawless MW; Mankan AK; Ryan AW; Norris S
    Hepatology; 2008 Jul; 48(1):344-5. PubMed ID: 18203149
    [No Abstract]   [Full Text] [Related]  

  • 18. Characteristics of HFE C282Y homozygotes younger than age 30 years.
    Barton JC; Felitti VJ; Lee P; Beutler E
    Acta Haematol; 2004; 112(4):219-21. PubMed ID: 15564736
    [No Abstract]   [Full Text] [Related]  

  • 19. Clinical implications of the hemochromatosis gene.
    Tavill AS
    N Engl J Med; 1999 Sep; 341(10):755-7. PubMed ID: 10471465
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical penetrance of hereditary hemochromatosis.
    Bacon BR; Britton RS
    N Engl J Med; 2008 Jan; 358(3):291-2. PubMed ID: 18199868
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.