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Journal Abstract Search

161 related items for PubMed ID: 22619055

  • 1. Adult-onset Alexander disease with an R66Q mutation in GFAP presented with severe vocal cord paralysis during sleep.
    Hida A, Ishiura H, Arai N, Fukuoka H, Hasuo K, Goto J, Uesaka Y, Tsuji S, Takeuchi S.
    J Neurol; 2012 Oct; 259(10):2234-6. PubMed ID: 22619055
    [No Abstract] [Full Text] [Related]

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  • 3. Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.
    Pareyson D, Fancellu R, Mariotti C, Romano S, Salmaggi A, Carella F, Girotti F, Gattellaro G, Carriero MR, Farina L, Ceccherini I, Savoiardo M.
    Brain; 2008 Sep; 131(Pt 9):2321-31. PubMed ID: 18684770
    [Abstract] [Full Text] [Related]

  • 4. Dominantly-inherited adult-onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene.
    Thyagarajan D, Chataway T, Li R, Gai WP, Brenner M.
    Mov Disord; 2004 Oct; 19(10):1244-8. PubMed ID: 15390001
    [Abstract] [Full Text] [Related]

  • 5. Familial adult-onset Alexander disease with a novel mutation (D78N) in the glial fibrillary acidic protein gene with unusual bilateral basal ganglia involvement.
    Wada Y, Yanagihara C, Nishimura Y, Namekawa M.
    J Neurol Sci; 2013 Aug 15; 331(1-2):161-4. PubMed ID: 23743246
    [Abstract] [Full Text] [Related]

  • 6. Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.
    Kaneko H, Hirose M, Katada S, Takahashi T, Naruse S, Tsuchiya M, Yoshida T, Nakagawa M, Onodera O, Nishizawa M, Ikeuchi T.
    Mov Disord; 2009 Jul 15; 24(9):1393-5. PubMed ID: 19412928
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  • 8. Parkinsonism phenotype in a family with adult onset Alexander disease and a novel mutation of GFAP.
    Vázquez-Justes D, Peñalva-García J, López R, Mitjana R, Begue R, González-Mingot C.
    Clin Neurol Neurosurg; 2020 Aug 15; 195():105893. PubMed ID: 32417628
    [No Abstract] [Full Text] [Related]

  • 9. A novel mutation in the GFAP gene in a familial adult onset Alexander disease.
    Salmaggi A, Botturi A, Lamperti E, Grisoli M, Fischetto R, Ceccherini I, Caroli F, Boiardi A.
    J Neurol; 2007 Sep 15; 254(9):1278-80. PubMed ID: 17703343
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  • 11. GFAP canonical transcript may not be suitable for the diagnosis of adult-onset Alexander disease.
    Pinto E Vairo F, Bertsch N, Klee EW, Gavrilova RH.
    Acta Neuropathol Commun; 2018 Oct 24; 6(1):112. PubMed ID: 30355306
    [No Abstract] [Full Text] [Related]

  • 12. Long-term follow-up of a case of adult-onset Alexander disease presenting with cognitive impairment as the initial symptom.
    Kawai Y, Hattori M, Mori K, Ieda T.
    Neurol India; 2017 Oct 24; 65(4):887-889. PubMed ID: 28681773
    [No Abstract] [Full Text] [Related]

  • 13. [Glial fibrillary acidic protein mutation in a Chinese girl with infantile Alexander disease].
    Ma HW, Lu JF, Jiang J, Chen LY, Niu GH, Wu BM, Kanazawa N, Tsujino S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 24; 22(1):79-81. PubMed ID: 15696488
    [Abstract] [Full Text] [Related]

  • 14. Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.
    Yoshida T, Sasayama H, Mizuta I, Okamoto Y, Yoshida M, Riku Y, Hayashi Y, Yonezu T, Takata Y, Ohnari K, Okuda S, Aiba I, Nakagawa M.
    Acta Neurol Scand; 2011 Aug 24; 124(2):104-8. PubMed ID: 20849398
    [Abstract] [Full Text] [Related]

  • 15. [A case of Alexander disease with dropped head syndrome].
    Maeda K, Iwai K, Kobayashi Y, Tsuji H, Yoshida T, Kobayashi Y.
    Rinsho Shinkeigaku; 2018 Mar 28; 58(3):198-201. PubMed ID: 29491332
    [Abstract] [Full Text] [Related]

  • 16. Adult onset Alexander disease presenting with progressive spastic paraplegia.
    Pedroso JL, Raskin S, Barsottini OG, Oliveira AS.
    Parkinsonism Relat Disord; 2014 Feb 28; 20(2):241-2. PubMed ID: 24188966
    [No Abstract] [Full Text] [Related]

  • 17. A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation.
    Kinoshita T, Imaizumi T, Miura Y, Fujimoto H, Ayabe M, Shoji H, Okamoto Y, Takashima H, Osame M, Nakagawa M.
    Neurosci Lett; 2003 Oct 30; 350(3):169-72. PubMed ID: 14550921
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  • 18. Acute onset of adult Alexander disease.
    Schmidt H, Kretzschmar B, Lingor P, Pauli S, Schramm P, Otto M, Ohlenbusch A, Brockmann K.
    J Neurol Sci; 2013 Aug 15; 331(1-2):152-4. PubMed ID: 23706596
    [Abstract] [Full Text] [Related]

  • 19. An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein.
    Ohnari K, Yamano M, Uozumi T, Hashimoto T, Tsuji S, Nakagawa M.
    J Neurol; 2007 Oct 15; 254(10):1390-4. PubMed ID: 17934883
    [Abstract] [Full Text] [Related]

  • 20. A novel mutation in the GFAP gene expands the phenotype of Alexander disease.
    Casasnovas C, Verdura E, Vélez V, Schlüter A, Pons-Escoda A, Homedes C, Ruiz M, Fourcade S, Launay N, Pujol A.
    J Med Genet; 2019 Dec 15; 56(12):846-849. PubMed ID: 31004048
    [Abstract] [Full Text] [Related]

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