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156 related items for PubMed ID: 12667993

  • 21. Mutations in HFE and TFR2 genes in a Spanish patient with hemochromatosis.
    Rueda Adel C, Grande NC, Fernández EA, Enríquez de Salamanca R, Sala LA, Jiménez MJ.
    Rev Esp Enferm Dig; 2011 Jul; 103(7):379-82. PubMed ID: 21770687
    [Abstract] [Full Text] [Related]

  • 22. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E, Cerani P, Rolandi V, Rovati A, Bergamaschi G.
    Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
    [Abstract] [Full Text] [Related]

  • 23. 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; 56(2):585-93. PubMed ID: 22383097
    [Abstract] [Full Text] [Related]

  • 24. Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients.
    Rahmani R, Naseri P, Safaroghli-Azar A, Tarighi S, Hosseini T, Hojjati MT.
    Transfus Clin Biol; 2019 Nov; 26(4):249-252. PubMed ID: 31679808
    [Abstract] [Full Text] [Related]

  • 25. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
    [Abstract] [Full Text] [Related]

  • 26. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr; 47(5):404-10. PubMed ID: 9510559
    [Abstract] [Full Text] [Related]

  • 27. 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
    [Abstract] [Full Text] [Related]

  • 28. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
    Loréal O, Ropert M, Mosser A, Déhais V, Deugnier Y, David V, Brissot P, Jouanolle AM.
    Presse Med; 2007 Sep; 36(9 Pt 2):1271-7. PubMed ID: 17521857
    [Abstract] [Full Text] [Related]

  • 29. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.
    Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
    [Abstract] [Full Text] [Related]

  • 30. Phenotypic expression of a novel C282Y/R226G compound heterozygous state in HFE hemochromatosis: molecular dynamics and biochemical studies.
    Cézard C, Rabbind Singh A, Le Gac G, Gourlaouen I, Ferec C, Rochette J.
    Blood Cells Mol Dis; 2014 Jan; 52(1):27-34. PubMed ID: 23953397
    [Abstract] [Full Text] [Related]

  • 31. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
    Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.
    Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018
    [Abstract] [Full Text] [Related]

  • 32. Hereditary hemochromatosis in north-eastern Romania.
    Voicu PM, Cojocariu C, Petrescu-Dănilă E, Stanciu C, Covic M, Rusu M, Trifan A.
    Rev Med Chir Soc Med Nat Iasi; 2010 Oct; 114(4):982-7. PubMed ID: 21495455
    [Abstract] [Full Text] [Related]

  • 33. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 34. [Non-HFE-related hereditary iron overload].
    Aguilar-Martinez P.
    Presse Med; 2007 Sep; 36(9 Pt 2):1279-91. PubMed ID: 17540536
    [Abstract] [Full Text] [Related]

  • 35. Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis.
    Canavese C, Bergamo D, Barbieri S, Timbaldi M, Thea A, Martina G, Damiani D, Fenoglio R, Donati-Marella B, Priolo G.
    Clin Nephrol; 2002 Dec; 58(6):438-44. PubMed ID: 12508966
    [Abstract] [Full Text] [Related]

  • 36. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote.
    Wallace DF, Dooley JS, Walker AP.
    Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824
    [Abstract] [Full Text] [Related]

  • 37. Effect of co-inheritance of β-thalassemia and hemochromatosis mutations on iron overload.
    López-Escribano H, Ferragut JF, Parera MM, Guix P, Castro JA, Ramon MM, Picornell A.
    Hemoglobin; 2012 Jun; 36(1):85-92. PubMed ID: 22122796
    [Abstract] [Full Text] [Related]

  • 38. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
    Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK.
    Gastroenterology; 2002 Mar; 122(3):646-51. PubMed ID: 11874997
    [Abstract] [Full Text] [Related]

  • 39. HFE mutations do not account for transfusional iron overload in patients with acute myeloid leukemia.
    Parkkila S, Niemelä O, Savolainen ER, Koistinen P.
    Transfusion; 2001 Jun; 41(6):828-31. PubMed ID: 11399828
    [Abstract] [Full Text] [Related]

  • 40. Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload.
    Pointon JJ, Viprakasit V, Miles KL, Livesey KJ, Steiner M, O'Riordan S, Hien TT, Merryweather-Clarke AT, Robson KJ.
    Blood Cells Mol Dis; 2003 Jun; 30(3):302-6. PubMed ID: 12737949
    [Abstract] [Full Text] [Related]

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