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Journal Abstract Search

186 related items for PubMed ID: 9696020

  • 1. 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]

  • 2. 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]

  • 3. 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 Aug; 33(1):35-9. PubMed ID: 15223008
    [Abstract] [Full Text] [Related]

  • 4. 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; 26(3):298-304. PubMed ID: 16584391
    [Abstract] [Full Text] [Related]

  • 5. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD, Flora K, Gross C, Rabkin JM, Corless CL.
    Am J Clin Pathol; 1998 May; 109(5):577-84. PubMed ID: 9576576
    [Abstract] [Full Text] [Related]

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

  • 7. [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]

  • 8. Presence of hemochromatosis-associated mutations in Hispanic patients with iron overload.
    Nieves-Santiago P, Cancel D, Canales D, Toro DH.
    P R Health Sci J; 2011 Sep 22; 30(3):135-8. PubMed ID: 21932715
    [Abstract] [Full Text] [Related]

  • 9. Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families.
    Adams PC, Campion ML, Gandon G, LeGall JY, David V, Jouanolle AM.
    Hepatology; 1997 Oct 22; 26(4):986-90. PubMed ID: 9328324
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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 Feb 13; 37(1):33-9. PubMed ID: 16762569
    [Abstract] [Full Text] [Related]

  • 12. Is there a threshold of hepatic iron concentration that leads to cirrhosis in C282Y hemochromatosis?
    Adams PC.
    Am J Gastroenterol; 2001 Feb 13; 96(2):567-9. PubMed ID: 11232708
    [Abstract] [Full Text] [Related]

  • 13. 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 13; 87(5):472-8. PubMed ID: 12010659
    [Abstract] [Full Text] [Related]

  • 14. [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis].
    Andrikovics H, Klein I, Kalmár L, Bors A, Jermendy G, Petri I, Kalász L, Váradi A, Tordai A.
    Orv Hetil; 1999 Nov 07; 140(45):2517-22. PubMed ID: 10586619
    [Abstract] [Full Text] [Related]

  • 15. Hereditary hemochromatosis in liver transplantation.
    Fiel MI, Schiano TD, Bodenheimer HC, Thung SN, King TW, Varma CR, Miller CM, Brunt EM, Starnes S, Prass C, Wolff RK, Bacon BR.
    Liver Transpl Surg; 1999 Jan 07; 5(1):50-6. PubMed ID: 9873093
    [Abstract] [Full Text] [Related]

  • 16. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Jan 07; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 17. Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy.
    Bartolo C, McAndrew PE, Sosolik RC, Cawley KA, Balcerzak SP, Brandt JT, Prior TW.
    Arch Pathol Lab Med; 1998 Jul 07; 122(7):633-7. PubMed ID: 9674544
    [Abstract] [Full Text] [Related]

  • 18. Association of Genetic Variant Linked to Hemochromatosis With Brain Magnetic Resonance Imaging Measures of Iron and Movement Disorders.
    Loughnan R, Ahern J, Tompkins C, Palmer CE, Iversen J, Thompson WK, Andreassen O, Jernigan T, Sugrue L, Dale A, Boyle MET, Fan CC.
    JAMA Neurol; 2022 Sep 01; 79(9):919-928. PubMed ID: 35913729
    [Abstract] [Full Text] [Related]

  • 19. The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
    Livesey KJ, Wimhurst VL, Carter K, Worwood M, Cadet E, Rochette J, Roberts AG, Pointon JJ, Merryweather-Clarke AT, Bassett ML, Jouanolle AM, Mosser A, David V, Poulton J, Robson KJ.
    J Med Genet; 2004 Jan 01; 41(1):6-10. PubMed ID: 14729817
    [Abstract] [Full Text] [Related]

  • 20. TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy.
    Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P.
    Blood Cells Mol Dis; 2014 Jan 01; 52(2-3):83-7. PubMed ID: 24055163
    [Abstract] [Full Text] [Related]

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