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Journal Abstract Search

190 related items for PubMed ID: 23812204

  • 1. 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; 52(13):1527-30. PubMed ID: 23812204
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox.
    Lindner U, Schuppan D, Schleithoff L, Habeck JO, Grodde T, Kirchhof K, Stoelzel U.
    Horm Metab Res; 2015 Apr; 47(4):303-8. PubMed ID: 25089372
    [Abstract] [Full Text] [Related]

  • 4. Deferasirox Might Be Effective for Microcytic Anemia and Neurological Symptoms Associated with Aceruloplasminemia: A Case Report and Review of the Literature.
    Miyake Z, Nakamagoe K, Yoshida K, Kondo T, Tamaoka A.
    Intern Med; 2020 Jul 15; 59(14):1755-1761. PubMed ID: 32238721
    [Abstract] [Full Text] [Related]

  • 5. Aceruloplasminaemia: a disorder of diabetes and neurodegeneration.
    Calder GL, Lee MH, Sachithanandan N, Bell S, Zeimer H, MacIsaac RJ.
    Intern Med J; 2017 Jan 15; 47(1):115-118. PubMed ID: 28076908
    [Abstract] [Full Text] [Related]

  • 6. Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia?
    Pelucchi S, Pelloni I, Arosio C, Mariani R, Piperno A.
    Blood Cells Mol Dis; 2016 Mar 15; 57():112-4. PubMed ID: 26777753
    [No Abstract] [Full Text] [Related]

  • 7. 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 15; 85(3):300-1. PubMed ID: 23557349
    [No Abstract] [Full Text] [Related]

  • 8. Neurodegeneration With Brain Iron Accumulation: A Novel Mutation in the Ceruloplasmin Gene.
    Stelten BML, van Ommen W, Keizer K.
    JAMA Neurol; 2019 Feb 01; 76(2):229-230. PubMed ID: 30383083
    [No Abstract] [Full Text] [Related]

  • 9. 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 01; 36(7):e423-5. PubMed ID: 25247888
    [Abstract] [Full Text] [Related]

  • 10. Aceruloplasminemia With Positive Ceruloplasm Gene Mutation.
    Kang HG, Kim M, Lee SC.
    JAMA Ophthalmol; 2016 Jul 14; 134(7):e160816. PubMed ID: 27416276
    [No Abstract] [Full Text] [Related]

  • 11. Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis.
    Vila Cuenca M, Marchi G, Barqué A, Esteban-Jurado C, Marchetto A, Giorgetti A, Chelban V, Houlden H, Wood NW, Piubelli C, Dorigatti Borges M, Martins de Albuquerque D, Yotsumoto Fertrin K, Jové-Buxeda E, Sanchez-Delgado J, Baena-Díez N, Burnyte B, Utkus A, Busti F, Kaubrys G, Suku E, Kowalczyk K, Karaszewski B, Porter JB, Pollard S, Eleftheriou P, Bignell P, Girelli D, Sanchez M.
    Int J Mol Sci; 2020 Mar 30; 21(7):. PubMed ID: 32235485
    [Abstract] [Full Text] [Related]

  • 12. Criteria for early identification of aceruloplasminemia.
    Ogimoto M, Anzai K, Takenoshita H, Kogawa K, Akehi Y, Yoshida R, Nakano M, Yoshida K, Ono J.
    Intern Med; 2011 Mar 30; 50(13):1415-8. PubMed ID: 21720062
    [Abstract] [Full Text] [Related]

  • 13. 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 30; 11 Suppl 2(Suppl 2):S14-S16. PubMed ID: 38400595
    [No Abstract] [Full Text] [Related]

  • 14. New mutation of the ceruloplasmin gene in the case of a neurologically asymptomatic patient with microcytic anaemia, obesity and supposed Wilson's disease.
    Ondrejkovičová M, Dražilová S, Drakulová M, Siles JL, Zemjarová Mezenská R, Jungová P, Fabián M, Rychlý B, Žigrai M.
    BMC Gastroenterol; 2020 Apr 07; 20(1):95. PubMed ID: 32264837
    [Abstract] [Full Text] [Related]

  • 15. Aceruloplasminemia: an update.
    Kono S.
    Int Rev Neurobiol; 2013 Apr 07; 110():125-51. PubMed ID: 24209437
    [Abstract] [Full Text] [Related]

  • 16. 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 07; 29(7):450-3. PubMed ID: 17307325
    [Abstract] [Full Text] [Related]

  • 17. Aceruloplasminemia and putaminal cavitation.
    Riboldi GM, Anstett K, Jain R, Lau H, Swope D.
    Parkinsonism Relat Disord; 2018 Jun 07; 51():121-123. PubMed ID: 29534945
    [No Abstract] [Full Text] [Related]

  • 18. Superficial siderosis associated with aceruloplasminemia. Case report.
    Matsushima A, Yoshida T, Yoshida K, Ohara S, Toyoshima Y, Kakita A, Ikeda S.
    J Neurol Sci; 2014 Apr 15; 339(1-2):231-4. PubMed ID: 24607334
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Aceruloplasminaemia: a rare but important cause of iron overload.
    Doyle A, Rusli F, Bhathal P.
    BMJ Case Rep; 2015 May 14; 2015():. PubMed ID: 25976187
    [Abstract] [Full Text] [Related]

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