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Journal Abstract Search

303 related items for PubMed ID: 19412928

  • 21. Alexander disease and megalencephalic leukoencephalopathy with subcortical cysts: leukodystrophies arising from astrocyte dysfunction.
    Gorospe JR, Maletkovic J.
    Ment Retard Dev Disabil Res Rev; 2006; 12(2):113-22. PubMed ID: 16807904
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  • 22. Alexander disease: combined gene analysis and MRI clarify pathogenesis and extend phenotype.
    Moser HW.
    Ann Neurol; 2005 Mar; 57(3):307-8. PubMed ID: 15732119
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  • 24. 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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  • 27. 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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  • 28. 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 15; 124(2):104-8. PubMed ID: 20849398
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  • 29. 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 15; 31(3):244-7. PubMed ID: 18584981
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  • 30. Familial adult-onset Alexander disease with a novel mutation (D78N) in the glial fibrillary acidic protein gene with unusual bilateral basal ganglia involvement.
    Wada Y, Yanagihara C, Nishimura Y, Namekawa M.
    J Neurol Sci; 2013 Aug 15; 331(1-2):161-4. PubMed ID: 23743246
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  • 32. A novel GFAP mutation in a type II (late-onset) Alexander disease patient.
    de Paiva AR, Freua F, Lucato LT, Parmera J, Dória D, Nóbrega PR, Olávio TR, Macedo-Souza LI, Kok F.
    J Neurol; 2016 Apr 15; 263(4):821-2. PubMed ID: 26914930
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  • 34. Adult onset Alexander disease presenting with progressive spastic paraplegia.
    Pedroso JL, Raskin S, Barsottini OG, Oliveira AS.
    Parkinsonism Relat Disord; 2014 Feb 15; 20(2):241-2. PubMed ID: 24188966
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  • 35. Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortex.
    Suzuki H, Yoshida T, Kitada M, Ichihashi J, Sasayama H, Nishikawa Y, Mistui Y, Nakagawa M, Kusunoki S.
    J Neurol; 2012 Mar 15; 259(3):457-61. PubMed ID: 21822933
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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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  • 37. 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 15; 33(4):194-8. PubMed ID: 12368989
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  • 38. 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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  • 39. Alexander disease: GFAP mutations unify young and old.
    Messing A, Brenner M.
    Lancet Neurol; 2003 Feb 15; 2(2):75. PubMed ID: 12849260
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  • 40. Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene.
    Chang KE, Pratt D, Mishra BB, Edwards N, Hallett M, Ray-Chaudhury A.
    Clin Neuropathol; 2015 Feb 15; 34(5):298-302. PubMed ID: 25997626
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