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Journal Abstract Search

321 related items for PubMed ID: 21940697

  • 1. An unusual presentation of juvenile Alexander disease.
    Osorio MJ, Risen S, Alper G.
    J Child Neurol; 2012 Apr; 27(4):507-10. PubMed ID: 21940697
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  • 3. 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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  • 4. 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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  • 6. 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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  • 7. 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 15; 131(Pt 9):2321-31. PubMed ID: 18684770
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  • 8. 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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  • 11. 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 15; 19(10):1244-8. PubMed ID: 15390001
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  • 14. 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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  • 16. 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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  • 17. [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 15; 22(1):79-81. PubMed ID: 15696488
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  • 18. Early mitochondrial dysfunction in an infant with Alexander disease.
    Cáceres-Marzal C, Vaquerizo J, Galán E, Fernández S.
    Pediatr Neurol; 2006 Oct 15; 35(4):293-6. PubMed ID: 16996408
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