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Journal Abstract Search

334 related items for PubMed ID: 15508811

  • 21. Hereditary hemochromatosis should be considered a conformational disorder.
    Lawless MW, Mankan AK, Norris S.
    Med Hypotheses; 2008; 70(4):783-4. PubMed ID: 17904763
    [Abstract] [Full Text] [Related]

  • 22. [Hereditary hemochromatosis].
    Niederau C.
    Med Klin (Munich); 2009 Dec 15; 104(12):931-46. PubMed ID: 20039160
    [Abstract] [Full Text] [Related]

  • 23. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.
    Schweiz Med Wochenschr; 2000 Aug 08; 130(31-32):1112-9. PubMed ID: 11008304
    [Abstract] [Full Text] [Related]

  • 24. Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases.
    Barton JC, Lee PL, West C, Bottomley SS.
    Am J Hematol; 2006 Oct 08; 81(10):760-7. PubMed ID: 16838333
    [Abstract] [Full Text] [Related]

  • 25. Hereditary hemochromatosis: implications for South Dakota physicians.
    Stampe C, Weiland K.
    S D Med; 2013 Jan 08; 66(1):15, 17-8. PubMed ID: 23342715
    [Abstract] [Full Text] [Related]

  • 26. Association of porphyria cutanea tarda with hereditary hemochromatosis.
    Mehrany K, Drage LA, Brandhagen DJ, Pittelkow MR.
    J Am Acad Dermatol; 2004 Aug 08; 51(2):205-11. PubMed ID: 15280838
    [Abstract] [Full Text] [Related]

  • 27. Iron-overload-related disease in HFE hereditary hemochromatosis.
    Allen KJ, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM.
    N Engl J Med; 2008 Jan 17; 358(3):221-30. PubMed ID: 18199861
    [Abstract] [Full Text] [Related]

  • 28. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC, Wiener HW, Acton RT, Go RC.
    Blood Cells Mol Dis; 2005 Jan 17; 34(1):38-47. PubMed ID: 15607698
    [Abstract] [Full Text] [Related]

  • 29. What is HFE haemochromatosis?
    Marjot T, Collier J, Ryan JD.
    Br J Hosp Med (Lond); 2016 Jun 17; 77(6):C91-5. PubMed ID: 27269766
    [No Abstract] [Full Text] [Related]

  • 30. Pitfalls in the genetic diagnosis of hereditary hemochromatosis.
    Jeffrey GP, Adams PC.
    Genet Test; 2000 Jun 17; 4(2):143-6. PubMed ID: 10953953
    [Abstract] [Full Text] [Related]

  • 31. Genetics of hemochromatosis.
    Cullen LM, Anderson GJ, Ramm GA, Jazwinska EC, Powell LW.
    Annu Rev Med; 1999 Jun 17; 50():87-98. PubMed ID: 10073265
    [Abstract] [Full Text] [Related]

  • 32. Recent advances in hemochromatosis: a 2015 update : a summary of proceedings of the 2014 conference held under the auspices of Hemochromatosis Australia.
    Ekanayake D, Roddick C, Powell LW.
    Hepatol Int; 2015 Apr 17; 9(2):174-82. PubMed ID: 25788196
    [Abstract] [Full Text] [Related]

  • 33. Hereditary hemochromatosis: pathophysiology, diagnosis, and management.
    Fowler C.
    Crit Care Nurs Clin North Am; 2008 Jun 17; 20(2):191-201, vi. PubMed ID: 18424348
    [Abstract] [Full Text] [Related]

  • 34. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
    Spínola C, Brehm A, Spínola H.
    Ann Hematol; 2011 Jan 17; 90(1):29-32. PubMed ID: 20714725
    [Abstract] [Full Text] [Related]

  • 35. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
    Larsen LE, Ellervik C, Appleyard M, Nordestgaard BG, Birgens H, Tybjaerg-Hansen A.
    Ugeskr Laeger; 2002 Sep 23; 164(39):4545-7. PubMed ID: 12380399
    [Abstract] [Full Text] [Related]

  • 36. A novel homozygous frameshift deletion c.471del of HFE associated with hemochromatosis.
    Cukjati M, Koren S, Curin Serbec V, Vidan-Jeras B, Rupreht R.
    Clin Genet; 2007 Apr 23; 71(4):350-3. PubMed ID: 17470136
    [Abstract] [Full Text] [Related]

  • 37. Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey.
    Yönal O, Hatirnaz O, Akyüz F, Köroğlu G, Ozbek U, Cefle K, Mungan Z.
    Turk J Gastroenterol; 2007 Mar 23; 18(1):53-7. PubMed ID: 17450498
    [Abstract] [Full Text] [Related]

  • 38. 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 23; 52(1):27-34. PubMed ID: 23953397
    [Abstract] [Full Text] [Related]

  • 39. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
    Cruz E, Vieira J, Almeida S, Lacerda R, Gartner A, Cardoso CS, Alves H, Porto G.
    BMC Med Genet; 2006 Mar 01; 7():16. PubMed ID: 16509978
    [Abstract] [Full Text] [Related]

  • 40. Coinheritance of hereditary spherocytosis and reversibility of cirrhosis in a young female patient with hereditary hemochromatosis.
    Höblinger A, Erdmann C, Strassburg CP, Sauerbruch T, Lammert F.
    Eur J Med Res; 2009 Apr 16; 14(4):182-4. PubMed ID: 19380292
    [Abstract] [Full Text] [Related]

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