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Journal Abstract Search

170 related items for PubMed ID: 10746346

  • 1. Inborn errors of metabolism: iron.
    Worwood M.
    Br Med Bull; 1999; 55(3):556-67. PubMed ID: 10746346
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  • 2. A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.
    Adams PC, Barton JC.
    J Hepatol; 2011 Aug; 55(2):453-8. PubMed ID: 21354228
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  • 3. Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis.
    Cotter PD, May A, Li L, Al-Sabah AI, Fitzsimons EJ, Cazzola M, Bishop DF.
    Blood; 1999 Mar 01; 93(5):1757-69. PubMed ID: 10029606
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  • 4. [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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  • 6. Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations.
    Beris P, Samii K, Darbellay R, Zoumbos N, Tsoplou P, Kourakli A, Preud'homme C, Fenaux P.
    Br J Haematol; 1999 Jan 05; 104(1):97-9. PubMed ID: 10027719
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  • 7. Hereditary hyperferritinaemia-cataract syndrome: a challenging diagnosis for the hepatogastroenterologist.
    Ferrante M, Geubel AP, Fevery J, Marogy G, Horsmans Y, Nevens F.
    Eur J Gastroenterol Hepatol; 2005 Nov 05; 17(11):1247-53. PubMed ID: 16215440
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  • 8. The ferroportin disease.
    Pietrangelo A.
    Blood Cells Mol Dis; 2004 Nov 05; 32(1):131-8. PubMed ID: 14757427
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  • 11. Epidemiology and diagnostic testing for hemochromatosis and iron overload.
    Adams PC.
    Int J Lab Hematol; 2015 May 05; 37 Suppl 1():25-30. PubMed ID: 25976957
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  • 12. Hereditary sideroblastic anemias: pathophysiology, diagnosis, and treatment.
    Camaschella C.
    Semin Hematol; 2009 Oct 05; 46(4):371-7. PubMed ID: 19786205
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  • 14. A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract.
    Girelli D, Olivieri O, De Franceschi L, Corrocher R, Bergamaschi G, Cazzola M.
    Br J Haematol; 1995 Aug 05; 90(4):931-4. PubMed ID: 7669675
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