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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 12483130

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  • 2. [Hemochromatosis--from an underdiagnosed curiosity to a common disease].
    Hagve TA, Asberg A, Ulvik R, Borch-Iohnsen B, Thorstensen K.
    Tidsskr Nor Laegeforen; 2009 Apr 30; 129(9):863-6. PubMed ID: 19415085
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  • 10. A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
    Koyama C, Wakusawa S, Hayashi H, Ueno T, Suzuki R, Yano M, Saito H, Okazaki T.
    Intern Med; 2005 Sep 30; 44(9):990-3. PubMed ID: 16258219
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  • 12. [Hereditary hemocromatosis].
    Franchini M, Veneri D.
    Recenti Prog Med; 2004 Oct 30; 95(10):457-62. PubMed ID: 15560291
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  • 13. Screening for hemochromatosis in asymptomatic subjects with or without a family history.
    Powell LW, Dixon JL, Ramm GA, Purdie DM, Lincoln DJ, Anderson GJ, Subramaniam VN, Hewett DG, Searle JW, Fletcher LM, Crawford DH, Rodgers H, Allen KJ, Cavanaugh JA, Bassett ML.
    Arch Intern Med; 2006 Feb 13; 166(3):294-301. PubMed ID: 16476869
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  • 14. [Fundamentals of the laboratory diagnosis in inherited hemochromatosis (literature survey)].
    Kazanets EG, Karamian NA.
    Klin Lab Diagn; 2004 Oct 13; (10):7-13. PubMed ID: 15584392
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  • 19. Iron overload without the C282Y mutation in patients with epilepsy.
    Ikeda M.
    J Neurol Neurosurg Psychiatry; 2001 Apr 13; 70(4):551-3. PubMed ID: 11254788
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  • 20. [Hemochromatosis: the importance of mutation screening in the family].
    ter Braak N, Erdkamp FL, van Deursen CT.
    Ned Tijdschr Geneeskd; 2009 Apr 18; 153(16):765-7. PubMed ID: 19469149
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