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Journal Abstract Search

218 related items for PubMed ID: 26777753

  • 1. Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia?
    Pelucchi S, Pelloni I, Arosio C, Mariani R, Piperno A.
    Blood Cells Mol Dis; 2016 Mar; 57():112-4. PubMed ID: 26777753
    [No Abstract] [Full Text] [Related]

  • 2. Novel ceruloplasmin mutation causing aceruloplasminemia with hepatic iron overload and diabetes without neurological symptoms.
    Rusticeanu M, Zimmer V, Schleithoff L, Wonney K, Viera J, Zimmer A, Hübschen U, Bohle RM, Grünhage F, Lammert F.
    Clin Genet; 2014 Mar; 85(3):300-1. PubMed ID: 23557349
    [No Abstract] [Full Text] [Related]

  • 3. 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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  • 4. [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; 41(11):769-775. PubMed ID: 32682623
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  • 6. 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]

  • 7. Combination-therapy with concurrent deferoxamine and deferiprone is effective in treating resistant cardiac iron-loading in aceruloplasminaemia.
    Badat M, Kaya B, Telfer P.
    Br J Haematol; 2015 Nov; 171(3):430-2. PubMed ID: 25855051
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  • 9. Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation.
    Finkenstedt A, Wolf E, Höfner E, Gasser BI, Bösch S, Bakry R, Creus M, Kremser C, Schocke M, Theurl M, Moser P, Schranz M, Bonn G, Poewe W, Vogel W, Janecke AR, Zoller H.
    J Hepatol; 2010 Dec; 53(6):1101-7. PubMed ID: 20801540
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  • 11. Concurrent β-thalassaemia trait and Southeast Asian ovalocytosis associated with clinically significant iron loading.
    Chen Y, Law HY, Tan GP, Ang AL.
    Blood Cells Mol Dis; 2017 Mar; 63():25-26. PubMed ID: 28024237
    [No Abstract] [Full Text] [Related]

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  • 15. Iron chelation therapy to prevent the manifestations of aceruloplasminemia.
    Bove F, Fasano A.
    Neurology; 2015 Sep 22; 85(12):1085-6. PubMed ID: 26311749
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  • 19. 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
    [No Abstract] [Full Text] [Related]

  • 20. Aceruloplasminemia in a Turkish adolescent with a novel mutation of ceruloplasmin gene: the first diagnosed case from Turkey.
    Meral Gunes A, Sezgin Evim M, Baytan B, Iwata A, Hida A, Avci R.
    J Pediatr Hematol Oncol; 2014 Oct 15; 36(7):e423-5. PubMed ID: 25247888
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