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Journal Abstract Search

209 related items for PubMed ID: 16055358

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Hemochromatosis in Italy in the last 30 years: role of genetic and acquired factors.
    Fracanzani AL, Piperno A, Valenti L, Fraquelli M, Coletti S, Maraschi A, Consonni D, Coviello E, Conte D, Fargion S.
    Hepatology; 2010 Feb; 51(2):501-10. PubMed ID: 20101754
    [Abstract] [Full Text] [Related]

  • 23. Prevalence of HFE mutations in California newborns.
    Hoppe C, Watson RM, Long CM, Lorey F, Robles L, Klitz W, Styles L, Vichinsky E.
    Pediatr Hematol Oncol; 2006 Sep; 23(6):507-16. PubMed ID: 16849282
    [Abstract] [Full Text] [Related]

  • 24. C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload.
    Jorquera F, Domínguez A, Díaz-Golpe V, Espinel J, Muñoz F, Herrera A, Fernández-Gundín MJ, Vivas S, Olcoz JL.
    Rev Esp Enferm Dig; 2001 May; 93(5):293-302. PubMed ID: 11488107
    [Abstract] [Full Text] [Related]

  • 25. Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC region.
    Sachot S, Moirand R, Jouanolle AM, Mosser J, Fergelot P, Deugnier Y, Brissot P, le Gall JY, David V.
    Blood Cells Mol Dis; 2001 May; 27(2):518-29. PubMed ID: 11500063
    [Abstract] [Full Text] [Related]

  • 26. Hemochromatosis-causing mutations C282Y and H63D are not risk factors for atherothrombotic cerebral infarction.
    Hruskovicová H, Milanez T, Kobal J, Potisk KP, Petrovic D, Peterlin B.
    Med Sci Monit; 2005 Jul; 11(7):BR248-52. PubMed ID: 15990686
    [Abstract] [Full Text] [Related]

  • 27. The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosis.
    Adams LA, Angulo P, Abraham SC, Torgerson H, Brandhagen D.
    Liver Int; 2006 Apr; 26(3):298-304. PubMed ID: 16584391
    [Abstract] [Full Text] [Related]

  • 28. [Polymorphism of the HFE gene associated with hereditary hemochromatosis in populations of Russia].
    Mikhaĭlova SV, Kobzev VF, Kulikov IV, Romashchenko AG, Khasnulin VI, Voevoda MI.
    Genetika; 2003 Jul; 39(7):988-95. PubMed ID: 12942784
    [Abstract] [Full Text] [Related]

  • 29. Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.
    Zamboni P, Tognazzo S, Izzo M, Pancaldi F, Scapoli GL, Liboni A, Gemmati D.
    J Vasc Surg; 2005 Aug; 42(2):309-14. PubMed ID: 16102632
    [Abstract] [Full Text] [Related]

  • 30. TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy.
    Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P.
    Blood Cells Mol Dis; 2014 Aug; 52(2-3):83-7. PubMed ID: 24055163
    [Abstract] [Full Text] [Related]

  • 31. [Iron storage disease].
    Horváth G, Dávid K.
    Orv Hetil; 2004 Sep 26; 145(39):1979-84. PubMed ID: 15553908
    [Abstract] [Full Text] [Related]

  • 32. Detection of the C282Y and H63D polymorphisms associated with hereditary hemochromatosis using the ABI 7500 fast real time PCR platform.
    Tafe LJ, Belloni DR, Tsongalis GJ.
    Diagn Mol Pathol; 2007 Jun 26; 16(2):112-5. PubMed ID: 17525682
    [Abstract] [Full Text] [Related]

  • 33. Hemochromatosis-associated gene mutations in patients with myelodysplastic syndromes with refractory anemia with ringed sideroblasts.
    Nearman ZP, Szpurka H, Serio B, Warshawksy I, Theil K, Lichtin A, Sekeres MA, Maciejewski JP.
    Am J Hematol; 2007 Dec 26; 82(12):1076-9. PubMed ID: 17654685
    [Abstract] [Full Text] [Related]

  • 34. 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 26; 125(5):674-8. PubMed ID: 15147384
    [Abstract] [Full Text] [Related]

  • 35. The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.
    Kallianpur AR, Hall LD, Yadav M, Byrne DW, Speroff T, Dittus RS, Haines JL, Christman BW, Summar ML.
    Bone Marrow Transplant; 2005 Jun 26; 35(12):1155-64. PubMed ID: 15834437
    [Abstract] [Full Text] [Related]

  • 36. Hemochromatosis: genetics helps to define a multifactorial disease.
    Burke W, Press N, McDonnell SM.
    Clin Genet; 1998 Jul 26; 54(1):1-9. PubMed ID: 9727731
    [Abstract] [Full Text] [Related]

  • 37. Mutation analysis in hereditary hemochromatosis.
    Beutler E, Gelbart T, West C, Lee P, Adams M, Blackstone R, Pockros P, Kosty M, Venditti CP, Phatak PD, Seese NK, Chorney KA, Ten Elshof AE, Gerhard GS, Chorney M.
    Blood Cells Mol Dis; 1996 Jul 26; 22(2):187-94; discussion 194a-194b. PubMed ID: 8931958
    [Abstract] [Full Text] [Related]

  • 38. Molecular epidemiology of HFE gene polymorphic variants (C282Y, H63D and S65C) in the population of Espírito Santo, Brazil.
    Alves LN, Santos EV, Stur E, Silva Conforti AM, Louro ID.
    Genet Mol Res; 2016 Apr 27; 15(2):. PubMed ID: 27173269
    [Abstract] [Full Text] [Related]

  • 39. 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 27; 14(1):158-63. PubMed ID: 15668490
    [Abstract] [Full Text] [Related]

  • 40. Haemochromatosis mutations in North-East Scotland.
    Miedzybrodzka Z, Loughlin S, Baty D, Terron A, Kelly K, Dean J, Greaves M, Pippard M, Haites N.
    Br J Haematol; 1999 Aug 27; 106(2):385-7. PubMed ID: 10460595
    [Abstract] [Full Text] [Related]

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