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Journal Abstract Search

278 related items for PubMed ID: 15732098

  • 21. 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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  • 24. A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis.
    Sakakibara T, Takahashi Y, Fukuda K, Inoue T, Kurosawa T, Nishikubo T, Shima M, Taoka T, Aida N, Tsujino S, Kanazawa N, Yoshioka A.
    Brain Dev; 2007 Sep; 29(8):525-8. PubMed ID: 17383133
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  • 26. Fluctuation of computed tomographic findings in white matter in Alexander's disease.
    Shiihara T, Kato M, Honma T, Ohtaki S, Sawaishi Y, Hayasaka K.
    J Child Neurol; 2002 Mar; 17(3):227-30. PubMed ID: 12026242
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  • 27. Alexander's disease: clinical, pathologic, and genetic features.
    Johnson AB, Brenner M.
    J Child Neurol; 2003 Sep; 18(9):625-32. PubMed ID: 14572141
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  • 28. 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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  • 30. 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; 52(12):1160-3. PubMed ID: 20964669
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  • 32. 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 Dec; 20(2):110-7. PubMed ID: 27442695
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  • 33. 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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  • 36. An unusual presentation of juvenile Alexander disease.
    Osorio MJ, Risen S, Alper G.
    J Child Neurol; 2012 Apr 15; 27(4):507-10. PubMed ID: 21940697
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  • 38. Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant.
    Melchionda L, Fang M, Wang H, Fugnanesi V, Morbin M, Liu X, Li W, Ceccherini I, Farina L, Savoiardo M, D'Adamo P, Zhang J, Costa A, Ravaglia S, Ghezzi D, Zeviani M.
    Orphanet J Rare Dis; 2013 May 01; 8():66. PubMed ID: 23634874
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  • 39. Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis.
    Shiroma N, Kanazawa N, Izumi M, Sugai K, Fukumizu M, Sasaki M, Hanaoka S, Kaga M, Tsujino S.
    J Hum Genet; 2001 May 01; 46(10):579-82. PubMed ID: 11587071
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  • 40. Alexander disease and megalencephalic leukoencephalopathy with subcortical cysts: leukodystrophies arising from astrocyte dysfunction.
    Gorospe JR, Maletkovic J.
    Ment Retard Dev Disabil Res Rev; 2006 May 01; 12(2):113-22. PubMed ID: 16807904
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