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Journal Abstract Search

268 related items for PubMed ID: 31717526

  • 1. Mild Iron Overload as Seen in Individuals Homozygous for the Alpha-1 Antitrypsin Pi*Z Variant Does Not Promote Liver Fibrogenesis in HFE Knockout Mice.
    Guldiken N, Hamesch K, Schuller SM, Aly M, Lindhauer C, Schneider CV, Fromme M, Trautwein C, Strnad P.
    Cells; 2019 Nov 09; 8(11):. PubMed ID: 31717526
    [Abstract] [Full Text] [Related]

  • 2. Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ Mutation.
    Hamesch K, Mandorfer M, Pereira VM, Moeller LS, Pons M, Dolman GE, Reichert MC, Schneider CV, Woditsch V, Voss J, Lindhauer C, Fromme M, Spivak I, Guldiken N, Zhou B, Arslanow A, Schaefer B, Zoller H, Aigner E, Reiberger T, Wetzel M, Siegmund B, Simões C, Gaspar R, Maia L, Costa D, Bento-Miranda M, van Helden J, Yagmur E, Bzdok D, Stolk J, Gleiber W, Knipel V, Windisch W, Mahadeva R, Bals R, Koczulla R, Barrecheguren M, Miravitlles M, Janciauskiene S, Stickel F, Lammert F, Liberal R, Genesca J, Griffiths WJ, Trauner M, Krag A, Trautwein C, Strnad P, European Alpha1-Liver Study Group.
    Gastroenterology; 2019 Sep 09; 157(3):705-719.e18. PubMed ID: 31121167
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  • 3. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
    Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P.
    Gut; 2002 Nov 09; 51(5):723-30. PubMed ID: 12377814
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  • 4. Liver Phenotypes of European Adults Heterozygous or Homozygous for Pi∗Z Variant of AAT (Pi∗MZ vs Pi∗ZZ genotype) and Noncarriers.
    Schneider CV, Hamesch K, Gross A, Mandorfer M, Moeller LS, Pereira V, Pons M, Kuca P, Reichert MC, Benini F, Burbaum B, Voss J, Gutberlet M, Woditsch V, Lindhauer C, Fromme M, Kümpers J, Bewersdorf L, Schaefer B, Eslam M, Bals R, Janciauskiene S, Carvão J, Neureiter D, Zhou B, Wöran K, Bantel H, Geier A, Dirrichs T, Stickel F, Teumer A, Verbeek J, Nevens F, Govaere O, Krawczyk M, Roskams T, Haybaeck J, Lurje G, Chorostowska-Wynimko J, Genesca J, Reiberger T, Lammert F, Krag A, George J, Anstee QM, Trauner M, Datz C, Gaisa NT, Denk H, Trautwein C, Aigner E, Strnad P, European Alpha-1 Liver Study Group.
    Gastroenterology; 2020 Aug 09; 159(2):534-548.e11. PubMed ID: 32376409
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  • 5. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun 09; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 6. Alpha-1 Antitrypsin Augmentation and the Liver Phenotype of Adults With Alpha-1 Antitrypsin Deficiency (Genotype Pi∗ZZ).
    Fromme M, Hamesch K, Schneider CV, Mandorfer M, Pons M, Thorhauge KH, Pereira V, Sperl J, Frankova S, Reichert MC, Benini F, Burbaum B, Kleinjans M, Amzou S, Rademacher L, Bewersdorf L, Verbeek J, Nevens F, Genesca J, Miravitlles M, Nuñez A, Schaefer B, Zoller H, Janciauskiene S, Waern J, Oliveira A, Maia L, Simões C, Mahadeva R, Fraughen DD, Trauner M, Krag A, Lammert F, Bals R, Gaisa NT, Aigner E, Griffiths WJ, Denk H, Teumer A, McElvaney NG, Turner AM, Trautwein C, Strnad P.
    Clin Gastroenterol Hepatol; 2024 Feb 09; 22(2):283-294.e5. PubMed ID: 37716616
    [Abstract] [Full Text] [Related]

  • 7. Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.
    Sikorska K, Romanowski T, Stalke P, Iżycka-Świeszewska E, Bielawski KP.
    Hepatobiliary Pancreat Dis Int; 2011 Jun 09; 10(3):270-5. PubMed ID: 21669570
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  • 10. HFE mutations in alpha-1-antitrypsin deficiency: an examination of cirrhotic explants.
    Lam M, Torbenson M, Yeh MM, Vivekanandan P, Ferrell L.
    Mod Pathol; 2010 May 09; 23(5):637-43. PubMed ID: 20208481
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  • 13. Alpha 1-antitrypsin mutations in NAFLD: high prevalence and association with altered iron metabolism but not with liver damage.
    Valenti L, Dongiovanni P, Piperno A, Fracanzani AL, Maggioni M, Rametta R, Loria P, Casiraghi MA, Suigo E, Ceriani R, Remondini E, Trombini P, Fargion S.
    Hepatology; 2006 Oct 09; 44(4):857-64. PubMed ID: 17006922
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  • 15. Non-Invasive Assessment and Management of Liver Involvement in Adults With Alpha-1 Antitrypsin Deficiency.
    Hamesch K, Strnad P.
    Chronic Obstr Pulm Dis; 2020 Jul 09; 7(3):260-271. PubMed ID: 32697896
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  • 16. Alcohol consumption and liver phenotype of individuals with alpha-1 antitrypsin deficiency.
    Fromme M, Schneider CV, Guldiken N, Amzou S, Luo Y, Pons M, Genesca J, Miravitlles M, Thorhauge KH, Mandorfer M, Waern J, Schneider KM, Sperl J, Frankova S, Bartel M, Zimmer H, Zorn M, Krag A, Turner A, Trautwein C, Strnad P.
    Liver Int; 2024 Oct 09; 44(10):2660-2671. PubMed ID: 39031304
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  • 17. HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity.
    Chitturi S, Weltman M, Farrell GC, McDonald D, Kench J, Liddle C, Samarasinghe D, Lin R, Abeygunasekera S, George J.
    Hepatology; 2002 Jul 09; 36(1):142-9. PubMed ID: 12085358
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  • 18. Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism.
    Gómez-Llorente C, Miranda-León MT, Blanco S, Gandia-Pla S, Gómez-Capilla JA, Fárez-Vidal ME.
    Ann Hematol; 2005 Oct 09; 84(10):650-5. PubMed ID: 15986199
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  • 19. Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice.
    Delima RD, Chua AC, Tirnitz-Parker JE, Gan EK, Croft KD, Graham RM, Olynyk JK, Trinder D.
    Hepatology; 2012 Aug 09; 56(2):585-93. PubMed ID: 22383097
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  • 20. 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
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