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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

691 related items for PubMed ID: 25976957

  • 41. Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.
    Badar S, Busti F, Ferrarini A, Xumerle L, Bozzini P, Capelli P, Pozzi-Mucelli R, Campostrini N, De Matteis G, Marin Vargas S, Giorgetti A, Delledonne M, Olivieri O, Girelli D.
    Am J Hematol; 2016 Jun; 91(4):420-5. PubMed ID: 26799139
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  • 42. Serial serum ferritin measurements in untreated HFE C282Y homozygotes in the Hemochromatosis and Iron Overload Screening Study.
    Adams PC, Reboussin DM, Barton JC, Acton RT, Speechley M, Leiendecker-Foster C, Meenan R, Passmore L, McLaren CE, McLaren GD, Gordeuk V, Dawkins F, Eckfeldt JH.
    Int J Lab Hematol; 2008 Aug; 30(4):300-5. PubMed ID: 18665827
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  • 44. The importance of screening for hemochromatosis.
    Dubois S, Kowdley KV.
    Arch Intern Med; 2003 Nov 10; 163(20):2424-6; author reply 2426. PubMed ID: 14609776
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  • 46. Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
    Acton RT, Barton JC, Snively BM, McLaren CE, Adams PC, Harris EL, Speechley MR, McLaren GD, Dawkins FW, Leiendecker-Foster C, Holup JL, Balasubramanyam A, Hemochromatosis and Iron Overload Screening Study Research Investigators.
    Ethn Dis; 2006 Nov 10; 16(4):815-21. PubMed ID: 17061732
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  • 47. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.
    N Engl J Med; 1999 Sep 02; 341(10):718-24. PubMed ID: 10471457
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  • 48. Screening for C282Y homozygosity in a Norwegian population (HUNT2): The sensitivity and specificity of transferrin saturation.
    Thorstensen K, Kvitland MA, Irgens WØ, Hveem K, Asberg A.
    Scand J Clin Lab Invest; 2010 Apr 02; 70(2):92-7. PubMed ID: 20073670
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  • 49. [Iron overload disease: recent findings].
    Licata A, Brucato V, Di Marco V, Barbaria F, Craxì A.
    Ann Ital Med Int; 2004 Apr 02; 19(3):145-54. PubMed ID: 15529941
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  • 50. A primer for predicting risk of disease in HFE-linked hemochromatosis.
    Adams PC, Walker AP, Acton RT.
    Genet Test; 2001 Apr 02; 5(4):311-6. PubMed ID: 11960576
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  • 51. Diagnosis and management of hereditary hemochromatosis.
    Salgia RJ, Brown K.
    Clin Liver Dis; 2015 Feb 02; 19(1):187-98. PubMed ID: 25454304
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  • 55. Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary-care population.
    Gordeuk VR, Reboussin DM, McLaren CE, Barton JC, Acton RT, McLaren GD, Harris EL, Reiss JA, Adams PC, Speechley M, Phatak PD, Sholinsky P, Eckfeldt JH, Chen WP, Passmore L, Dawkins FW.
    Am J Hematol; 2008 Aug 02; 83(8):618-26. PubMed ID: 18429050
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  • 56. EASL clinical practice guidelines for HFE hemochromatosis.
    European Association For The Study Of The Livereasl@easloffice.eu.
    J Hepatol; 2010 Jul 02; 53(1):3-22. PubMed ID: 20471131
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  • 57. Examining the clinical use of hemochromatosis genetic testing.
    Lanktree MB, Lanktree BB, Paré G, Waye JS, Sadikovic B, Crowther MA.
    Can J Gastroenterol Hepatol; 2015 Jul 02; 29(1):41-5. PubMed ID: 25706573
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  • 58. HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.
    Acton RT, Barton JC.
    Genet Test; 2001 Jul 02; 5(4):299-306. PubMed ID: 11960574
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  • 59. 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 Jul 02; 133(2):155-61. PubMed ID: 25277871
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  • 60. [Hereditary hemochromatosis].
    Dantas W.
    Rev Gastroenterol Peru; 2001 Jul 02; 21(1):42-55. PubMed ID: 12170286
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