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Journal Abstract Search

720 related items for PubMed ID: 18684770

  • 1. 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]

  • 2. 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; 124(2):104-8. PubMed ID: 20849398
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  • 3. Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.
    Stumpf E, Masson H, Duquette A, Berthelet F, McNabb J, Lortie A, Lesage J, Montplaisir J, Brais B, Cossette P.
    Arch Neurol; 2003 Sep; 60(9):1307-12. PubMed ID: 12975300
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  • 4. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
    Li R, Johnson AB, Salomons G, Goldman JE, Naidu S, Quinlan R, Cree B, Ruyle SZ, Banwell B, D'Hooghe M, Siebert JR, Rolf CM, Cox H, Reddy A, Gutiérrez-Solana LG, Collins A, Weller RO, Messing A, van der Knaap MS, Brenner M.
    Ann Neurol; 2005 Mar; 57(3):310-26. PubMed ID: 15732097
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  • 5. Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.
    Namekawa M, Takiyama Y, Aoki Y, Takayashiki N, Sakoe K, Shimazaki H, Taguchi T, Tanaka Y, Nishizawa M, Saito K, Matsubara Y, Nakano I.
    Ann Neurol; 2002 Dec; 52(6):779-85. PubMed ID: 12447932
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  • 7. 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
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  • 8. Clinical and genetic study in Chinese patients with Alexander disease.
    Ye Wu, Qiang Gu, Jingmin Wang, Yanling Yang, Xiru Wu, Yuwu Jiang.
    J Child Neurol; 2008 Feb 15; 23(2):173-7. PubMed ID: 18079314
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  • 10. An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.
    Asahina N, Okamoto T, Sudo A, Kanazawa N, Tsujino S, Saitoh S.
    Brain Dev; 2006 Mar 15; 28(2):131-3. PubMed ID: 16168593
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  • 11. TRH therapy in a patient with juvenile Alexander disease.
    Ishigaki K, Ito Y, Sawaishi Y, Kodaira K, Funatsuka M, Hattori N, Nakano K, Saito K, Osawa M.
    Brain Dev; 2006 Nov 15; 28(10):663-7. PubMed ID: 16774812
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  • 13. 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
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  • 14. Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander disease.
    Bachetti T, Caroli F, Bocca P, Prigione I, Balbi P, Biancheri R, Filocamo M, Mariotti C, Pareyson D, Ravazzolo R, Ceccherini I.
    Eur J Hum Genet; 2008 Apr 15; 16(4):462-70. PubMed ID: 18197187
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  • 15. Adult-onset Alexander disease with progressive ataxia and palatal tremor.
    Howard KL, Hall DA, Moon M, Agarwal P, Newman E, Brenner M.
    Mov Disord; 2008 Jan 15; 23(1):118-22. PubMed ID: 17960815
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  • 19. Alexander disease with periventricular calcification: a novel mutation of the GFAP gene.
    Jefferson RJ, Absoud M, Jain R, Livingston JH, VAN DER Knaap MS, Jayawant S.
    Dev Med Child Neurol; 2010 Dec 15; 52(12):1160-3. PubMed ID: 20964669
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  • 20. Increased levels of GFAP in the cerebrospinal fluid in three subtypes of genetically confirmed Alexander disease.
    Kyllerman M, Rosengren L, Wiklund LM, Holmberg E.
    Neuropediatrics; 2005 Oct 15; 36(5):319-23. PubMed ID: 16217707
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