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Journal Abstract Search

278 related items for PubMed ID: 15732098

  • 1. Unusual variants of Alexander's disease.
    van der Knaap MS, Salomons GS, Li R, Franzoni E, Gutiérrez-Solana LG, Smit LM, Robinson R, Ferrie CD, Cree B, Reddy A, Thomas N, Banwell B, Barkhof F, Jakobs C, Johnson A, Messing A, Brenner M.
    Ann Neurol; 2005 Mar; 57(3):327-38. PubMed ID: 15732098
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  • 4. 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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  • 6. 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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  • 7. 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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  • 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 28; 60(9):1307-12. PubMed ID: 12975300
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  • 13. [Juvenile form of Alexander's disease - a case confirmed by detection of mutation in GFAP gene].
    Kmieć T, Bilska M, Mierzewska H, Jurkiewicz E, Jóźwiak S.
    Neurol Neurochir Pol; 2007 Sep 28; 41(3):267-71. PubMed ID: 17629821
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  • 14. Tumor-like enlargement of the optic chiasm in an infant with Alexander disease.
    Mignot C, Desguerre I, Burglen L, Hertz-Pannier L, Renaldo F, Gadisseux JF, Gallet S, Pham-Dinh D, Boespflug-Tanguy O, Rodriguez D.
    Brain Dev; 2009 Mar 28; 31(3):244-7. PubMed ID: 18584981
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  • 15. 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 28; 131(Pt 9):2321-31. PubMed ID: 18684770
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  • 18. 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 28; 28(10):663-7. PubMed ID: 16774812
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  • 19. 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 28; 124(2):104-8. PubMed ID: 20849398
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