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PUBMED FOR HANDHELDS

Journal Abstract Search


235 related items for PubMed ID: 14636642

  • 21. Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload.
    Zaahl MG, Merryweather-Clarke AT, Kotze MJ, van der Merwe S, Warnich L, Robson KJ.
    Hum Genet; 2004 Oct; 115(5):409-17. PubMed ID: 15338274
    [Abstract] [Full Text] [Related]

  • 22. A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in China.
    Zhang W, Xu A, Li Y, Zhao S, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Nan Y, You H, Jia J, Ou X, Huang J, China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group.
    Liver Int; 2019 Jun; 39(6):1120-1127. PubMed ID: 30500107
    [Abstract] [Full Text] [Related]

  • 23. African Americans at risk for increased iron stores or liver disease.
    Dawkins FW, Gordeuk VR, Snively BM, Lovato L, Barton JC, Acton RT, McLaren GD, Leiendecker-Foster C, McLaren CE, Adams PC, Speechley M, Harris EL, Jackson S, Thomson EJ.
    Am J Med; 2007 Aug; 120(8):734.e1-9. PubMed ID: 17679134
    [Abstract] [Full Text] [Related]

  • 24. African iron overload.
    Gordeuk VR.
    Semin Hematol; 2002 Oct; 39(4):263-9. PubMed ID: 12382201
    [Abstract] [Full Text] [Related]

  • 25. A novel mutation in ferroportin implicated in iron overload.
    Wallace DF, Dixon JL, Ramm GA, Anderson GJ, Powell LW, Subramaniam VN.
    J Hepatol; 2007 May; 46(5):921-6. PubMed ID: 17383046
    [Abstract] [Full Text] [Related]

  • 26. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.
    Eur J Haematol; 2001 Aug; 67(2):110-8. PubMed ID: 11722599
    [Abstract] [Full Text] [Related]

  • 27. Rare causes of hereditary iron overload.
    Ponka P.
    Semin Hematol; 2002 Oct; 39(4):249-62. PubMed ID: 12382200
    [Abstract] [Full Text] [Related]

  • 28. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186
    [Abstract] [Full Text] [Related]

  • 29. Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).
    Cazzola M, Cremonesi L, Papaioannou M, Soriani N, Kioumi A, Charalambidou A, Paroni R, Romtsou K, Levi S, Ferrari M, Arosio P, Christakis J.
    Br J Haematol; 2002 Nov 28; 119(2):539-46. PubMed ID: 12406098
    [Abstract] [Full Text] [Related]

  • 30. Multi-organ iron overload in an African-American man with ALAS2 R452S and SLC40A1 R561G.
    Sussman NL, Lee PL, Dries AM, Schwartz MR, Barton JC.
    Acta Haematol; 2008 Nov 28; 120(3):168-73. PubMed ID: 19066423
    [Abstract] [Full Text] [Related]

  • 31. Ferroportin disease: pathogenesis, diagnosis and treatment.
    Pietrangelo A.
    Haematologica; 2017 Dec 28; 102(12):1972-1984. PubMed ID: 29101207
    [Abstract] [Full Text] [Related]

  • 32. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3).
    Devalia V, Carter K, Walker AP, Perkins SJ, Worwood M, May A, Dooley JS.
    Blood; 2002 Jul 15; 100(2):695-7. PubMed ID: 12091367
    [Abstract] [Full Text] [Related]

  • 33. Iron overload due to mutations in ferroportin.
    De Domenico I, Ward DM, Musci G, Kaplan J.
    Haematologica; 2006 Jan 15; 91(1):92-5. PubMed ID: 16434376
    [Abstract] [Full Text] [Related]

  • 34. Novel mutations of the ferroportin gene (SLC40A1): analysis of 56 consecutive patients with unexplained iron overload.
    Pelucchi S, Mariani R, Salvioni A, Bonfadini S, Riva A, Bertola F, Trombini P, Piperno A.
    Clin Genet; 2008 Feb 15; 73(2):171-8. PubMed ID: 18177470
    [Abstract] [Full Text] [Related]

  • 35. The role of genetic factors in patients with hepatocellular carcinoma and iron overload - a prospective series of 234 patients.
    Funakoshi N, Chaze I, Alary AS, Tachon G, Cunat S, Giansily-Blaizot M, Bismuth M, Larrey D, Pageaux GP, Schved JF, Donnadieu-Rigole H, Blanc P, Aguilar-Martinez P.
    Liver Int; 2016 May 15; 36(5):746-54. PubMed ID: 26474245
    [Abstract] [Full Text] [Related]

  • 36. Long-term phlebotomy successfully alleviated hepatic iron accumulation in a ferroportin disease patient with a mutation in SLC40A1: a case report.
    Nishina S, Tomiyama Y, Ikuta K, Tatsumi Y, Toki Y, Kato A, Kato K, Yoshioka N, Sasaki K, Hara Y, Hino K.
    BMC Gastroenterol; 2021 Mar 05; 21(1):111. PubMed ID: 33673803
    [Abstract] [Full Text] [Related]

  • 37. G80S-linked ferroportin disease: classical ferroportin disease in an Asian family and reclassification of the mutant as iron transport defective.
    McDonald CJ, Wallace DF, Ostini L, Bell SJ, Demediuk B, Subramaniam VN.
    J Hepatol; 2011 Mar 05; 54(3):538-44. PubMed ID: 21094556
    [Abstract] [Full Text] [Related]

  • 38. 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 05; 51(5):723-30. PubMed ID: 12377814
    [Abstract] [Full Text] [Related]

  • 39. [Genetic iron overloads and hepatic insulin-resistance iron overload syndrome: an update].
    Ruivard M.
    Rev Med Interne; 2009 Jan 05; 30(1):35-42. PubMed ID: 18584923
    [Abstract] [Full Text] [Related]

  • 40. Clinicopathological study of Japanese patients with genetic iron overload syndromes.
    Hattori A, Miyajima H, Tomosugi N, Tatsumi Y, Hayashi H, Wakusawa S.
    Pathol Int; 2012 Sep 05; 62(9):612-8. PubMed ID: 22924847
    [Abstract] [Full Text] [Related]


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