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42. The ocular motor features of adult-onset alexander disease: a case and review of the literature. Pfeffer G, Abegg M, Vertinsky AT, Ceccherini I, Caroli F, Barton JJ. J Neuroophthalmol; 2011 Jun; 31(2):155-9. PubMed ID: 21403579 [Abstract] [Full Text] [Related]
43. An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein. Ohnari K, Yamano M, Uozumi T, Hashimoto T, Tsuji S, Nakagawa M. J Neurol; 2007 Oct; 254(10):1390-4. PubMed ID: 17934883 [Abstract] [Full Text] [Related]
45. Aggregate formation analysis of GFAPR416W found in one case of Alexander disease. Tulyeu J, Tamaura M, Jimbo E, Shimbo H, Takano K, Iai M, Yamashita S, Goto T, Aida N, Tokuhiro E, Yamagata T, Osaka H. Brain Dev; 2019 Feb; 41(2):195-200. PubMed ID: 30213442 [Abstract] [Full Text] [Related]
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53. Infantile-onset Alexander disease: a genetically proven case with mild clinical course in a 6-year-old Indian boy. Ramesh K, Sharma S, Kumar A, Salomons GS, van der Knaap MS, Gulati S. J Child Neurol; 2013 Mar 15; 28(3):396-8. PubMed ID: 22566711 [Abstract] [Full Text] [Related]
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57. An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant. Dotti MT, Buccoliero R, Lee A, Gorospe JR, Flint D, Galluzzi P, Bianchi S, D'Eramo C, Naidu S, Federico A, Brenner M. J Neurol; 2009 Apr 01; 256(4):679-82. PubMed ID: 19444543 [No Abstract] [Full Text] [Related]
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60. Focus on molecules: glial fibrillary acidic protein (GFAP). Sarthy V. Exp Eye Res; 2007 Mar 01; 84(3):381-2. PubMed ID: 16563382 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]