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Journal Abstract Search

265 related items for PubMed ID: 15465095

  • 1. Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.
    Shiihara T, Sawaishi Y, Adachi M, Kato M, Hayasaka K.
    J Neurol Sci; 2004 Oct 15; 225(1-2):125-7. PubMed ID: 15465095
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  • 2. 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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  • 3. 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 15; 57(3):327-38. PubMed ID: 15732098
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  • 4. 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 15; 53(1):118-20. PubMed ID: 12509855
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  • 8. Adult Alexander's disease without leukoencephalopathy.
    Salvi F, Aoki Y, Della Nave R, Vella A, Pastorelli F, Scaglione C, Matsubara Y, Mascalchi M.
    Ann Neurol; 2005 Nov 15; 58(5):813-4. PubMed ID: 16240361
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  • 11. Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.
    Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T.
    Pediatr Neurol; 2008 Jan 15; 38(1):50-2. PubMed ID: 18054694
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  • 12. 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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  • 13. Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease.
    Kawai M, Sakai N, Miyake S, Tsukamoto H, Akagi M, Inui K, Mushiake S, Taniike M, Ozono K.
    Brain Dev; 2006 Jan 15; 28(1):60-2. PubMed ID: 16168595
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