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Journal Abstract Search

168 related items for PubMed ID: 15737888

  • 1. Role of ferritin and ferroportin genes in unexplained hyperferritinaemia.
    Cazzola M.
    Best Pract Res Clin Haematol; 2005 Jun; 18(2):251-63. PubMed ID: 15737888
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  • 2. Dual diagnoses of hereditary hyperferritinaemia-cataract syndrome and hereditary haemochromatosis.
    Hughes M, Vosylius P.
    Clin Lab Haematol; 2006 Oct; 28(5):357-9. PubMed ID: 16999731
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  • 3. Two Dutch families with hereditary hyperferritinaemia-cataract syndrome and heterozygosity for an HFE-related haemochromatosis gene mutation.
    Simsek S, Nanayakkara PW, Keek JM, Faber LM, Bruin KF, Pals G.
    Neth J Med; 2003 Sep; 61(9):291-5. PubMed ID: 14692443
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  • 4. The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
    Politou M, Kalotychou V, Pissia M, Rombos Y, Sakellaropoulos N, Papanikolaou G.
    Haematologica; 2004 Apr; 89(4):490-2. PubMed ID: 15075083
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  • 9. [Diagnosis of 5 patients with possible primary hemochromatosis].
    Jacobs EM, de Vries RA, Elving LD, Stalenhoef AF, Swinkels DW.
    Ned Tijdschr Geneeskd; 2003 Apr 05; 147(14):666-70. PubMed ID: 12712652
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  • 10. Hyperferritinaemia not always a sign of iron overload.
    Loffeld RJ.
    Acta Gastroenterol Belg; 2007 Apr 05; 70(4):360-2. PubMed ID: 18330093
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  • 11. [Hereditary hyperferritinaemia-cataract syndrome].
    van der Klooster JM.
    Ned Tijdschr Geneeskd; 2003 Sep 27; 147(39):1923-8. PubMed ID: 14560693
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  • 12. Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
    Townsend A, Drakesmith H.
    Lancet; 2002 Mar 02; 359(9308):786-90. PubMed ID: 11888608
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  • 13. Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations.
    Hetet G, Devaux I, Soufir N, Grandchamp B, Beaumont C.
    Blood; 2003 Sep 01; 102(5):1904-10. PubMed ID: 12730114
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  • 14. Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.
    Lachlan KL, Temple IK, Mumford AD.
    Eur J Hum Genet; 2004 Oct 01; 12(10):790-6. PubMed ID: 15280904
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  • 15. Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assay.
    Thurlow V, Vadher B, Bomford A, DeLord C, Kannengiesser C, Beaumont C, Grandchamp B.
    Ann Clin Biochem; 2012 May 01; 49(Pt 3):302-5. PubMed ID: 22535864
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  • 16. [Hereditary haemochromatosis: novel genes, novel diseases and hepcidin].
    Bergmans JP, Kemna EH, Janssen MC, Jacobs EM, Stalenhoef AF, Marx JJ, Swinkels DW.
    Ned Tijdschr Geneeskd; 2007 May 19; 151(20):1121-7. PubMed ID: 17557668
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  • 19. 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
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  • 20. A primer for predicting risk of disease in HFE-linked hemochromatosis.
    Adams PC, Walker AP, Acton RT.
    Genet Test; 2001 Apr 28; 5(4):311-6. PubMed ID: 11960576
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