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Journal Abstract Search

791 related items for PubMed ID: 15280838

  • 1. Association of porphyria cutanea tarda with hereditary hemochromatosis.
    Mehrany K, Drage LA, Brandhagen DJ, Pittelkow MR.
    J Am Acad Dermatol; 2004 Aug; 51(2):205-11. PubMed ID: 15280838
    [Abstract] [Full Text] [Related]

  • 2. [Role of the hemochromatosis gene in prophyria cutanea tarda. Prospective study of 56 cases].
    Skowron F, Bérard F, Grézard P, Wolf F, Morel Y, Perrot H.
    Ann Dermatol Venereol; 2001 May; 128(5):600-4. PubMed ID: 11427792
    [Abstract] [Full Text] [Related]

  • 3. Porphyria cutanea tarda associated with Cys282Tyr mutation in HFE gene in hereditary hemochromatosis: a case report and review of the literature.
    Young LC.
    Cutis; 2007 Nov; 80(5):415-8. PubMed ID: 18189029
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  • 4. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M, de Salamanca RE, Morales P, Martínez-Laso J, Fontanellas A, Castro MJ, Rojo R, Moscoso J, Zamora J, Serrano-Vela JI, Arnaiz-Villena A.
    J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
    [Abstract] [Full Text] [Related]

  • 5. 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
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  • 6. Precipitating factors of porphyria cutanea tarda in Brazil with emphasis on hemochromatosis gene (HFE) mutations. Study of 60 patients.
    Vieira FM, Nakhle MC, Abrantes-Lemos CP, Cançado EL, Reis VM.
    An Bras Dermatol; 2013 Dec; 88(4):530-40. PubMed ID: 24068123
    [Abstract] [Full Text] [Related]

  • 7. Hemochromatosis (HFE) gene mutations and hepatitis C virus infection as risk factors for porphyria cutanea tarda in Hungarian patients.
    Nagy Z, Kószó F, Pár A, Emri G, Horkay I, Horányi M, Karádi O, Rumi G, Morvay M, Varga V, Dobozy A, Mózsik G.
    Liver Int; 2004 Feb; 24(1):16-20. PubMed ID: 15101996
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  • 8. The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients.
    Stuart KA, Busfield F, Jazwinska EC, Gibson P, Butterworth LA, Cooksley WG, Powell LW, Crawford DH.
    J Hepatol; 1998 Mar; 28(3):404-9. PubMed ID: 9551677
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  • 9. [Mutations of hemochromatosis gene in volunteer blood donors and Chilean porphyria cutanea tarda patients].
    Wolff CF, Armas RM, Frank J, Poblete PG.
    Medicina (B Aires); 2006 Mar; 66(5):421-6. PubMed ID: 17137171
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  • 10. [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]

  • 11. HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France.
    Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou JJ.
    Br J Dermatol; 2001 Mar 22; 144(3):533-9. PubMed ID: 11260010
    [Abstract] [Full Text] [Related]

  • 12. The prevalence of HFE C282Y gene mutation is increased in Spanish patients with porphyria cutanea tarda without hepatitis C virus infection.
    Toll A, Celis R, Ozalla MD, Bruguera M, Herrero C, Ercilla MG.
    J Eur Acad Dermatol Venereol; 2006 Nov 22; 20(10):1201-6. PubMed ID: 17062032
    [Abstract] [Full Text] [Related]

  • 13. Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda.
    Roberts AG, Whatley SD, Morgan RR, Worwood M, Elder GH.
    Lancet; 1997 Feb 01; 349(9048):321-3. PubMed ID: 9024376
    [Abstract] [Full Text] [Related]

  • 14. Porphyria cutanea tarda, C282Y, H63D and S65C HFE gene mutations and hepatitis C infection: a study from southern France.
    Chiavérini C, Halimi G, Ouzan D, Halfon P, Ortonne JP, Lacour JP.
    Dermatology; 2003 Feb 01; 206(3):212-6. PubMed ID: 12673077
    [Abstract] [Full Text] [Related]

  • 15. Porphyria cutanea tarda, hepatitis C, and HFE gene mutations in North America.
    Bonkovsky HL, Poh-Fitzpatrick M, Pimstone N, Obando J, Di Bisceglie A, Tattrie C, Tortorelli K, LeClair P, Mercurio MG, Lambrecht RW.
    Hepatology; 1998 Jun 01; 27(6):1661-9. PubMed ID: 9620340
    [Abstract] [Full Text] [Related]

  • 16. Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study.
    Cribier B, Chiaverini C, Dali-Youcef N, Schmitt M, Grima M, Hirth C, Lacour JP, Chosidow O.
    Dermatology; 2009 Jun 01; 218(1):15-21. PubMed ID: 19001803
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