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Journal Abstract Search

136 related items for PubMed ID: 12010659

  • 1. High prevalence of a screening-detected, HFE-unrelated, mild idiopathic iron overload in Northern Italy.
    Barosi G, Salvaneschi L, Grasso M, Martinetti M, Marchetti M, Bodini U, Reggiani A, D'Agostino F, Nalli G, Degiuli A, De Silvestri A, Arbustini E.
    Haematologica; 2002 May; 87(5):472-8. PubMed ID: 12010659
    [Abstract] [Full Text] [Related]

  • 2. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 May; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 3. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
    Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R.
    Haematologica; 2002 Mar; 87(3):242-5. PubMed ID: 11869934
    [Abstract] [Full Text] [Related]

  • 4. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry.
    Kowdley KV, Brandhagen DJ, Gish RG, Bass NM, Weinstein J, Schilsky ML, Fontana RJ, McCashland T, Cotler SJ, Bacon BR, Keeffe EB, Gordon F, Polissar N, National Hemochromatosis Transplant Registry.
    Gastroenterology; 2005 Aug; 129(2):494-503. PubMed ID: 16083706
    [Abstract] [Full Text] [Related]

  • 5. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C, Opazo S, Murga MJ, Martínez-Castro P.
    Eur J Haematol; 2007 Jan; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 6. Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.
    Zanella A, Bianchi P, Iurlo A, Boschetti C, Taioli E, Vercellati C, Zappa M, Fermo E, Tavazzi D, Sampietro M.
    Blood Cells Mol Dis; 2001 Jan; 27(3):653-61. PubMed ID: 11482880
    [Abstract] [Full Text] [Related]

  • 7. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.
    De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C.
    Haematologica; 2003 Apr; 88(4):396-401. PubMed ID: 12681966
    [Abstract] [Full Text] [Related]

  • 8. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients.
    Potekhina ES, Lavrov AV, Samokhodskaya LM, Efimenko AY, Balatskiy AV, Baev AA, Litvinova MM, Nikitina LA, Shipulin GA, Bochkov NP, Tkachuk VA, Bochkov VN.
    Blood Cells Mol Dis; 2005 Apr; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 9. Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.
    De Gobbi M, D'Antico S, Castagno F, Testa D, Merlini R, Bondi A, Camaschella C.
    Haematologica; 2004 Oct; 89(10):1161-7. PubMed ID: 15477198
    [Abstract] [Full Text] [Related]

  • 10. HFE genotypes and dietary heme iron: no evidence of strong gene-nutrient interaction on serum ferritin concentrations in middle-aged women.
    van der A DL, Peeters PH, Grobbee DE, Roest M, Voorbij HA, van der Schouw YT.
    Nutr Metab Cardiovasc Dis; 2006 Jan; 16(1):60-8. PubMed ID: 16399493
    [Abstract] [Full Text] [Related]

  • 11. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P, Milman N.
    Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

  • 12. Relation of HFE gene mutations, high iron stores and early onset coronary artery disease.
    Nassar BA, Zayed EM, Title LM, O'Neill BJ, Bata IR, Kirkland SA, Dunn J, Dempsey GI, Tan MH, Johnstone DE.
    Can J Cardiol; 1998 Feb; 14(2):215-20. PubMed ID: 9520858
    [Abstract] [Full Text] [Related]

  • 13. Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry.
    Pozzato G, Zorat F, Nascimben F, Gregorutti M, Comar C, Baracetti S, Vatta S, Bevilacqua E, Belgrano A, Crovella S, Amoroso A.
    Eur J Hum Genet; 2001 Jun; 9(6):445-51. PubMed ID: 11436126
    [Abstract] [Full Text] [Related]

  • 14. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects.
    Cruz E, Melo G, Lacerda R, Almeida S, Porto G.
    Blood Cells Mol Dis; 2006 Jun; 37(1):33-9. PubMed ID: 16762569
    [Abstract] [Full Text] [Related]

  • 15. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation.
    Shaheen NJ, Bacon BR, Grimm IS.
    Hepatology; 1998 Aug; 28(2):526-9. PubMed ID: 9696020
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Disease-related conditions in relatives of patients with hemochromatosis.
    Bulaj ZJ, Ajioka RS, Phillips JD, LaSalle BA, Jorde LB, Griffen LM, Edwards CQ, Kushner JP.
    N Engl J Med; 2000 Nov 23; 343(21):1529-35. PubMed ID: 11087882
    [Abstract] [Full Text] [Related]

  • 18. Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.
    Milman N, Fenger K, Graudal NA, Nielsen LS.
    Dan Med Bull; 1994 Jun 23; 41(3):366-70. PubMed ID: 7924465
    [Abstract] [Full Text] [Related]

  • 19. 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 23; 93(5):293-302. PubMed ID: 11488107
    [Abstract] [Full Text] [Related]

  • 20. Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y.
    Barton JC, Barton JC, Acton RT.
    PLoS One; 2022 May 23; 17(7):e0271973. PubMed ID: 35895739
    [Abstract] [Full Text] [Related]

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