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PUBMED FOR HANDHELDS

Journal Abstract Search

259 related items for PubMed ID: 18651828

  • 21.
    ; . PubMed ID:
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  • 22. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct; 70(4):294-300. PubMed ID: 17767550
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  • 23.
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  • 24. Hemochromatosis mutations in the general population: iron overload progression rate.
    Andersen RV, Tybjaerg-Hansen A, Appleyard M, Birgens H, Nordestgaard BG.
    Blood; 2004 Apr 15; 103(8):2914-9. PubMed ID: 15070663
    [Abstract] [Full Text] [Related]

  • 25. Predicting C282Y homozygote genotype for hemochromatosis using serum ferritin and transferrin saturation values from 44,809 participants of the HEIRS study.
    Lim A, Speechley M, Adams PC.
    Can J Gastroenterol Hepatol; 2014 Oct 15; 28(9):502-4. PubMed ID: 25314357
    [Abstract] [Full Text] [Related]

  • 26. Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
    McLaren GD, Gordeuk VR.
    Hematology Am Soc Hematol Educ Program; 2009 Oct 15; ():195-206. PubMed ID: 20008199
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  • 27. Expression of the HFE hemochromatosis gene in a community-based population of elderly women.
    Rossi E, Kuek C, Beilby JP, Jeffrey GP, Devine A, Prince RL.
    J Gastroenterol Hepatol; 2004 Oct 15; 19(10):1150-4. PubMed ID: 15377292
    [Abstract] [Full Text] [Related]

  • 28. Iron-overload-related disease in HFE hereditary hemochromatosis.
    Allen KJ, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM.
    N Engl J Med; 2008 Jan 17; 358(3):221-30. PubMed ID: 18199861
    [Abstract] [Full Text] [Related]

  • 29. HFE genotype in patients with hemochromatosis and other liver diseases.
    Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK.
    Ann Intern Med; 1999 Jun 15; 130(12):953-62. PubMed ID: 10383365
    [Abstract] [Full Text] [Related]

  • 30. 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 Jun 15; 16(4):815-21. PubMed ID: 17061732
    [Abstract] [Full Text] [Related]

  • 31. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.
    Eur J Haematol; 2001 Aug 15; 67(2):110-8. PubMed ID: 11722599
    [Abstract] [Full Text] [Related]

  • 32. Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening Study.
    Barton JC, Acton RT, Lovato L, Speechley MR, McLaren CE, Harris EL, Reboussin DM, Adams PC, Dawkins FW, Gordeuk VR, Walker AP, Hemochromatosis and Iron Overload Screening Study Research Investigators.
    Clin Genet; 2006 Jan 15; 69(1):48-57. PubMed ID: 16451136
    [Abstract] [Full Text] [Related]

  • 33. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.
    Br J Haematol; 2001 Aug 15; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 34. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis.
    Walsh A, Dixon JL, Ramm GA, Hewett DG, Lincoln DJ, Anderson GJ, Subramaniam VN, Dodemaide J, Cavanaugh JA, Bassett ML, Powell LW.
    Clin Gastroenterol Hepatol; 2006 Nov 15; 4(11):1403-10. PubMed ID: 16979952
    [Abstract] [Full Text] [Related]

  • 35. Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening.
    Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, Eckfeldt JH, McLaren CE, Reiss JA, McLaren GD, Reboussin DM, Gordeuk VR, Speechley MR, Press RD, Dawkins FW, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    Am J Hematol; 2008 Feb 15; 83(2):126-32. PubMed ID: 17726683
    [Abstract] [Full Text] [Related]

  • 36. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 15; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 37. HFE C282Y homozygotes have reduced low-density lipoprotein cholesterol: the Atherosclerosis Risk in Communities (ARIC) Study.
    Pankow JS, Boerwinkle E, Adams PC, Guallar E, Leiendecker-Foster C, Rogowski J, Eckfeldt JH.
    Transl Res; 2008 Jul 15; 152(1):3-10. PubMed ID: 18593631
    [Abstract] [Full Text] [Related]

  • 38. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
    Barton JC, Lafreniere SA, Leiendecker-Foster C, Li H, Acton RT, Press RD, Eckfeldt JH.
    Am J Hematol; 2009 Nov 15; 84(11):710-4. PubMed ID: 19787796
    [Abstract] [Full Text] [Related]

  • 39. Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene.
    Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E.
    Mayo Clin Proc; 2002 Jun 15; 77(6):522-30. PubMed ID: 12059121
    [Abstract] [Full Text] [Related]

  • 40. 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 Jun 15; 4(6):436-40. PubMed ID: 14671617
    [Abstract] [Full Text] [Related]

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