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PUBMED FOR HANDHELDS

Journal Abstract Search


268 related items for PubMed ID: 11464482

  • 21.
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  • 22. Treatment of symptomatic heterozygous aceruloplasminemia with oral zinc sulphate.
    Kuhn J, Bewermeyer H, Miyajima H, Takahashi Y, Kuhn KF, Hoogenraad TU.
    Brain Dev; 2007 Aug; 29(7):450-3. PubMed ID: 17307325
    [Abstract] [Full Text] [Related]

  • 23. [A case of hereditary ceruloplasmin deficiency with hemosiderosis].
    Nakane S, Shirabe S, Suenaga A, Yoshimura T, Nakamura T.
    Rinsho Shinkeigaku; 1999 Aug; 39(2-3):347-51. PubMed ID: 10391079
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  • 24. Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.
    Logan JI, Harveyson KB, Wisdom GB, Hughes AE, Archbold GP.
    QJM; 1994 Nov; 87(11):663-70. PubMed ID: 7820540
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  • 27. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration.
    Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N.
    Neurology; 1987 May; 37(5):761-7. PubMed ID: 3574673
    [Abstract] [Full Text] [Related]

  • 28. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T, Tirouche YD, Abaoub-Germain A, Theodore F.
    Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
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  • 29.
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  • 30. Hepatic iron overload or cirrhosis may occur in acquired copper deficiency and is likely mediated by hypoceruloplasminemia.
    Thackeray EW, Sanderson SO, Fox JC, Kumar N.
    J Clin Gastroenterol; 2011 Feb; 45(2):153-8. PubMed ID: 20502350
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  • 31.
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  • 32. [Aceruloplasminemia (hereditary ceruloplasmin deficiency) and diabetes mellitus].
    Momoki T, Terauchi Y.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():100-4. PubMed ID: 17022509
    [No Abstract] [Full Text] [Related]

  • 33. Increased lipid peroxidation and mitochondrial dysfunction in aceruloplasminemia brains.
    Miyajima H, Kono S, Takahashi Y, Sugimoto M.
    Blood Cells Mol Dis; 2002 Sep 28; 29(3):433-8. PubMed ID: 12547232
    [Abstract] [Full Text] [Related]

  • 34.
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  • 36. Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia.
    Klomp LW, Gitlin JD.
    Hum Mol Genet; 1996 Dec 28; 5(12):1989-96. PubMed ID: 8968753
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  • 37.
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  • 38. Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia.
    Zanardi A, Conti A, Cremonesi M, D'Adamo P, Gilberti E, Apostoli P, Cannistraci CV, Piperno A, David S, Alessio M.
    EMBO Mol Med; 2018 Jan 28; 10(1):91-106. PubMed ID: 29183916
    [Abstract] [Full Text] [Related]

  • 39. Aceruloplasminemia in an asymptomatic patient with a new mutation. Diagnosis and family genetic analysis.
    Pérez-Aguilar F, Burguera JA, Benlloch S, Berenguer M, Rayón JM.
    J Hepatol; 2005 Jun 28; 42(6):947-9. PubMed ID: 15885371
    [Abstract] [Full Text] [Related]

  • 40.
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