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Journal Abstract Search

179 related items for PubMed ID: 24920245

  • 21. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH.
    Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565
    [Abstract] [Full Text] [Related]

  • 22. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.
    Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
    [Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186
    [Abstract] [Full Text] [Related]

  • 25. Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases.
    Barton JC, Lee PL, West C, Bottomley SS.
    Am J Hematol; 2006 Oct 28; 81(10):760-7. PubMed ID: 16838333
    [Abstract] [Full Text] [Related]

  • 26. Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.
    Mendes AI, Ferro A, Martins R, Picanço I, Gomes S, Cerqueira R, Correia M, Nunes AR, Esteves J, Fleming R, Faustino P.
    Ann Hematol; 2009 Mar 28; 88(3):229-34. PubMed ID: 18762941
    [Abstract] [Full Text] [Related]

  • 27. 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 28; 89(10):1161-7. PubMed ID: 15477198
    [Abstract] [Full Text] [Related]

  • 28. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
    Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    Genet Test; 2007 Oct 28; 11(3):269-75. PubMed ID: 17949288
    [Abstract] [Full Text] [Related]

  • 29. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ.
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr 28; 30(4):223-8. PubMed ID: 19731820
    [Abstract] [Full Text] [Related]

  • 30. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.
    Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.
    Hematol J; 2003 Apr 28; 4(6):436-40. PubMed ID: 14671617
    [Abstract] [Full Text] [Related]

  • 31. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 28; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 32. HFE gene mutations in patients with altered iron metabolism in Argentina.
    Rossetti MV, Méndez M, Afonso S, Gerez E, Batlle A, Muñoz A, Parera V.
    Cell Mol Biol (Noisy-le-grand); 2009 Jul 01; 55(2):31-5. PubMed ID: 19656448
    [Abstract] [Full Text] [Related]

  • 33. Clinical impact of HFE mutations in Japanese patients with chronic hepatitis C.
    Ishizu Y, Katano Y, Honda T, Hayashi K, Ishigami M, Itoh A, Hirooka Y, Nakano I, Goto H.
    J Gastroenterol Hepatol; 2012 Jun 01; 27(6):1112-6. PubMed ID: 22098610
    [Abstract] [Full Text] [Related]

  • 34. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
    de Tayrac M, Roth MP, Jouanolle AM, Coppin H, le Gac G, Piperno A, Férec C, Pelucchi S, Scotet V, Bardou-Jacquet E, Ropert M, Bouvet R, Génin E, Mosser J, Deugnier Y.
    J Hepatol; 2015 Mar 01; 62(3):664-72. PubMed ID: 25457201
    [Abstract] [Full Text] [Related]

  • 35. 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 01; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 36. Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.
    Tomatsu S, Orii KO, Fleming RE, Holden CC, Waheed A, Britton RS, Gutierrez MA, Velez-Castrillon S, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 2003 Dec 23; 100(26):15788-93. PubMed ID: 14673107
    [Abstract] [Full Text] [Related]

  • 37. Correlates of hepcidin and NTBI according to HFE status in patients referred to a liver centre.
    Ryan E, Ryan JD, Russell J, Coughlan B, Tjalsma H, Swinkels DW, Stewart S, Crowe JP.
    Acta Haematol; 2015 Dec 23; 133(2):155-61. PubMed ID: 25277871
    [Abstract] [Full Text] [Related]

  • 38. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G.
    Z Gastroenterol; 2003 Nov 23; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 39. Effect of co-inheritance of β-thalassemia and hemochromatosis mutations on iron overload.
    López-Escribano H, Ferragut JF, Parera MM, Guix P, Castro JA, Ramon MM, Picornell A.
    Hemoglobin; 2012 Nov 23; 36(1):85-92. PubMed ID: 22122796
    [Abstract] [Full Text] [Related]

  • 40. Hereditary hemochromatosis in north-eastern Romania.
    Voicu PM, Cojocariu C, Petrescu-Dănilă E, Stanciu C, Covic M, Rusu M, Trifan A.
    Rev Med Chir Soc Med Nat Iasi; 2010 Nov 23; 114(4):982-7. PubMed ID: 21495455
    [Abstract] [Full Text] [Related]

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