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Journal Abstract Search

249 related items for PubMed ID: 25864092

  • 1. Movement disorders and brain iron overload in a new subtype of aceruloplasminemia.
    Melgari JM, Marano M, Quattrocchi CC, Piperno A, Arosio C, Frontali M, Nuovo S, Siotto M, Salomone G, Altavilla R, di Biase L, Scrascia F, Squitti R, Vernieri F.
    Parkinsonism Relat Disord; 2015 Jun; 21(6):658-60. PubMed ID: 25864092
    [No Abstract] [Full Text] [Related]

  • 2. Central nervous system involvement in a rare genetic iron overload disorder.
    Bethlehem C, van Harten B, Hoogendoorn M.
    Neth J Med; 2010 Oct; 68(10):316-8. PubMed ID: 21071777
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  • 5. Aceruloplasminemia With Positive Ceruloplasm Gene Mutation.
    Kang HG, Kim M, Lee SC.
    JAMA Ophthalmol; 2016 Jul 14; 134(7):e160816. PubMed ID: 27416276
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  • 6. Aceruloplasminemia and putaminal cavitation.
    Riboldi GM, Anstett K, Jain R, Lau H, Swope D.
    Parkinsonism Relat Disord; 2018 Jun 14; 51():121-123. PubMed ID: 29534945
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  • 8. Extending the aceruloplasminemia phenotype: NBIA on imaging and acanthocytosis, yet only minor neurological findings.
    Kassubek R, Uttner I, Schönfeldt-Lecuona C, Kassubek J, Connemann BJ.
    J Neurol Sci; 2017 May 15; 376():151-152. PubMed ID: 28431603
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  • 9. [Aceruloplasminemia, a rare condition not to be overlooked].
    Lobbes H, Reynaud Q, Mainbourg S, Lega JC, Durieu I, Durupt S.
    Rev Med Interne; 2020 Nov 15; 41(11):769-775. PubMed ID: 32682623
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  • 10. 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 15; 29(7):450-3. PubMed ID: 17307325
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  • 12. Seizures in Hereditary Aceruloplasminemia.
    Marano M, Bove F, Ricci L, Rohani M, Di Lazzaro V, Assenza G, Fasano A.
    Can J Neurol Sci; 2021 Jan 15; 48(1):144-147. PubMed ID: 32741407
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  • 14. Clinical relevance of heterozygosis for aceruloplasminemia.
    Borges MD, de Albuquerque DM, Lanaro C, Costa FF, Fertrin KY.
    Am J Med Genet B Neuropsychiatr Genet; 2019 Jun 15; 180(4):266-271. PubMed ID: 30901137
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  • 15. Ceruloplasmin deficiency does not induce macrophagic iron overload: lessons from a new rat model of hereditary aceruloplasminemia.
    Kenawi M, Rouger E, Island ML, Leroyer P, Robin F, Rémy S, Tesson L, Anegon I, Nay K, Derbré F, Brissot P, Ropert M, Cavey T, Loréal O.
    FASEB J; 2019 Dec 15; 33(12):13492-13502. PubMed ID: 31560858
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  • 16. Effectiveness of oral iron chelator treatment with deferasirox in an aceruloplasminemia patient with a novel ceruloplasmin gene mutation.
    Suzuki Y, Yoshida K, Aburakawa Y, Kuroda K, Kimura T, Terada T, Kono S, Miyajima H, Yahara O.
    Intern Med; 2013 Dec 15; 52(13):1527-30. PubMed ID: 23812204
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  • 18. Aceruloplasminemia: Unique Clinical and MRI Findings in a Patient with a Novel Frameshift Mutation.
    Colucci F, Barca S, Cilia R, De Franco V, Elia AE, Golfrè Andreasi N, Romito L, Telese R, Braccia A, Leta V, Grisoli M, Panteghini C, Garavaglia B, Devigili G, Eleopra R.
    Mov Disord Clin Pract; 2024 Aug 15; 11 Suppl 2(Suppl 2):S14-S16. PubMed ID: 38400595
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