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Journal Abstract Search

154 related items for PubMed ID: 15223008

  • 1. DMT1 genetic variability is not responsible for phenotype variability in hereditary hemochromatosis.
    Kelleher T, Ryan E, Barrett S, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2004; 33(1):35-9. PubMed ID: 15223008
    [Abstract] [Full Text] [Related]

  • 2. 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; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. Increased DMT1 but not IREG1 or HFE mRNA following iron depletion therapy in hereditary haemochromatosis.
    Kelleher T, Ryan E, Barrett S, Sweeney M, Byrnes V, O'Keane C, Crowe J.
    Gut; 2004 Aug; 53(8):1174-9. PubMed ID: 15247188
    [Abstract] [Full Text] [Related]

  • 6. [Significance and prevalence of the C282Y gene mutation of primary hemochromatosis in the pathogenesis of pophyria cutanea tarda].
    Malina L, Zd'árský E, Dandová S, Michalíková H, Cerná M, Cimburová M.
    Cas Lek Cesk; 2000 Nov 22; 139(23):728-30. PubMed ID: 11191743
    [Abstract] [Full Text] [Related]

  • 7. Duodenal Dcytb and hephaestin mRNA expression are not significantly modulated by variations in body iron homeostasis.
    Gleeson F, Ryan E, Barrett S, Russell J, Kelleher B, Crowe J.
    Blood Cells Mol Dis; 2005 Nov 22; 35(3):303-8. PubMed ID: 16137899
    [Abstract] [Full Text] [Related]

  • 8. 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 22; 26(3):298-304. PubMed ID: 16584391
    [Abstract] [Full Text] [Related]

  • 9. Increased duodenal expression of divalent metal transporter 1 and iron-regulated gene 1 in cirrhosis.
    Stuart KA, Anderson GJ, Frazer DM, Murphy TL, Powell LW, Fletcher LM, Crawford DH.
    Hepatology; 2004 Feb 22; 39(2):492-9. PubMed ID: 14768003
    [Abstract] [Full Text] [Related]

  • 10. 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 Feb 22; 27(2):518-29. PubMed ID: 11500063
    [Abstract] [Full Text] [Related]

  • 11. Is there a threshold of hepatic iron concentration that leads to cirrhosis in C282Y hemochromatosis?
    Adams PC.
    Am J Gastroenterol; 2001 Feb 22; 96(2):567-9. PubMed ID: 11232708
    [Abstract] [Full Text] [Related]

  • 12. Relationship between gene expression of duodenal iron transporters and iron stores in hemochromatosis subjects.
    Nelson JE, Mugford VR, Kilcourse E, Wang RS, Kowdley KV.
    Am J Physiol Gastrointest Liver Physiol; 2010 Jan 22; 298(1):G57-62. PubMed ID: 19892936
    [Abstract] [Full Text] [Related]

  • 13. 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 22; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 14. 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 22; 93(5):293-302. PubMed ID: 11488107
    [Abstract] [Full Text] [Related]

  • 15. Intestinal expression of genes involved in iron absorption in humans.
    Rolfs A, Bonkovsky HL, Kohlroser JG, McNeal K, Sharma A, Berger UV, Hediger MA.
    Am J Physiol Gastrointest Liver Physiol; 2002 Apr 22; 282(4):G598-607. PubMed ID: 11897618
    [Abstract] [Full Text] [Related]

  • 16. Screening for hemochromatosis in asymptomatic subjects with or without a family history.
    Powell LW, Dixon JL, Ramm GA, Purdie DM, Lincoln DJ, Anderson GJ, Subramaniam VN, Hewett DG, Searle JW, Fletcher LM, Crawford DH, Rodgers H, Allen KJ, Cavanaugh JA, Bassett ML.
    Arch Intern Med; 2006 Feb 13; 166(3):294-301. PubMed ID: 16476869
    [Abstract] [Full Text] [Related]

  • 17. Compound heterozygosity for haemochromatosis gene mutations and hepatic iron overload in allogeneic bone marrow transplant recipients.
    Grigg AP, Bhathal PS.
    Pathology; 2001 Feb 13; 33(1):44-9. PubMed ID: 11280607
    [Abstract] [Full Text] [Related]

  • 18. 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 13; 35(12):1155-64. PubMed ID: 15834437
    [Abstract] [Full Text] [Related]

  • 19. A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload.
    Bardou-Jacquet E, Island ML, Jouanolle AM, Détivaud L, Fatih N, Ropert M, Brissot E, Mosser A, Maisonneuve H, Brissot P, Loréal O.
    Blood Cells Mol Dis; 2011 Dec 15; 47(4):243-8. PubMed ID: 21871825
    [Abstract] [Full Text] [Related]

  • 20. [Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards].
    Zdárský E, Horák J, Stríteský J, Heirler F.
    Cas Lek Cesk; 1999 Aug 23; 138(16):497-9. PubMed ID: 10566227
    [Abstract] [Full Text] [Related]

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