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Journal Abstract Search

439 related items for PubMed ID: 15732097

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  • 3. 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; 23(2):173-7. PubMed ID: 18079314
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  • 5. 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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  • 6. Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.
    Hartmann H, Herchenbach J, Stephani U, Ledaal P, Donnerstag F, Lücke T, Das AM, Christen HJ, Hagedorn M, Meins M.
    Neuropediatrics; 2007 Jun; 38(3):143-7. PubMed ID: 17985264
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  • 9. Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients.
    Meins M, Brockmann K, Yadav S, Haupt M, Sperner J, Stephani U, Hanefeld F.
    Neuropediatrics; 2002 Aug; 33(4):194-8. PubMed ID: 12368989
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  • 10. 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(10):663-7. PubMed ID: 16774812
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  • 12. 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; 28(1):60-2. PubMed ID: 16168595
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  • 13. 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; 26(3):206-8. PubMed ID: 15030911
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  • 17. 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; 53(1):118-20. PubMed ID: 12509855
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  • 18. Alexander disease - astrogliopathy considered as leukodystrophy - experience of an institution.
    Mierzewska H, Mierzewska-Schmidt M, Salomons GS, Dudzińska M, Szczepanik E.
    Dev Period Med; 2016 Jan; 20(2):110-7. PubMed ID: 27442695
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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; 124(2):104-8. PubMed ID: 20849398
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  • 20. 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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