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Journal Abstract Search


303 related items for PubMed ID: 17805552

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  • 4. 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; 23(1):118-22. PubMed ID: 17960815
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  • 5. Review of Alexander disease: beyond the classical concept of leukodystrophy.
    Sawaishi Y.
    Brain Dev; 2009 Aug; 31(7):493-8. PubMed ID: 19386454
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  • 8. 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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  • 9. 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 15; 60(9):1307-12. PubMed ID: 12975300
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  • 10. 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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  • 11. 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 15; 52(6):779-85. PubMed ID: 12447932
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  • 14. 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 15; 57(3):310-26. PubMed ID: 15732097
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  • 15. Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.
    van der Knaap MS, Ramesh V, Schiffmann R, Blaser S, Kyllerman M, Gholkar A, Ellison DW, van der Voorn JP, van Dooren SJ, Jakobs C, Barkhof F, Salomons GS.
    Neurology; 2006 Feb 28; 66(4):494-8. PubMed ID: 16505300
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  • 16. A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.
    Suzuki Y, Kanazawa N, Takenaka J, Okumura A, Negoro T, Tsujino S.
    Brain Dev; 2004 Apr 28; 26(3):206-8. PubMed ID: 15030911
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  • 19. Atypical focal MRI lesions in a case of juvenile Alexander's disease.
    Probst EN, Hagel C, Weisz V, Nagel S, Wittkugel O, Zeumer H, Kohlschütter A.
    Ann Neurol; 2003 Jan 28; 53(1):118-20. PubMed ID: 12509855
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