Similar articles for PMID: 23743246

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1

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. Wada Y, et al. J Neurol Sci. 2013 Aug 15;331(1-2):161-4. doi: 10.1016/j.jns.2013.05.019. Epub 2013 Jun 4. J Neurol Sci. 2013. PMID: 23743246 Free article.

2

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.

Pareyson D, Fancellu R, Mariotti C, Romano S, Salmaggi A, Carella F, Girotti F, Gattellaro G, Carriero MR, Farina L, Ceccherini I, Savoiardo M. Pareyson D, et al. Brain. 2008 Sep;131(Pt 9):2321-31. doi: 10.1093/brain/awn178. Epub 2008 Aug 6. Brain. 2008. PMID: 18684770 Review.

3

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. Yoshida T, et al. Acta Neurol Scand. 2011 Aug;124(2):104-8. doi: 10.1111/j.1600-0404.2010.01427.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849398

4

Acute onset of adult Alexander disease.

Schmidt H, Kretzschmar B, Lingor P, Pauli S, Schramm P, Otto M, Ohlenbusch A, Brockmann K. Schmidt H, et al. J Neurol Sci. 2013 Aug 15;331(1-2):152-4. doi: 10.1016/j.jns.2013.05.006. Epub 2013 May 23. J Neurol Sci. 2013. PMID: 23706596

5

[Adult onset Alexander disease with a novel variant (S398F) in the glial fibrillary acidic protein gene].

Sueda Y, Takahashi T, Ochi K, Ohtsuki T, Namekawa M, Kohriyama T, Takiyama Y, Matsumoto M. Sueda Y, et al. Rinsho Shinkeigaku. 2009 Jun;49(6):358-63. doi: 10.5692/clinicalneurol.49.358. Rinsho Shinkeigaku. 2009. PMID: 19618846 Review. Japanese.

6

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. Stumpf E, et al. Arch Neurol. 2003 Sep;60(9):1307-12. doi: 10.1001/archneur.60.9.1307. Arch Neurol. 2003. PMID: 12975300

7

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. Ohnari K, et al. J Neurol. 2007 Oct;254(10):1390-4. doi: 10.1007/s00415-007-0557-0. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934883

8

Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature.

Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I. Namekawa M, et al. BMC Neurol. 2010 Apr 1;10:21. doi: 10.1186/1471-2377-10-21. BMC Neurol. 2010. PMID: 20359319 Free PMC article. Review.

9

An autopsied case of adult-onset bulbospinalform Alexander disease with a novel S393R mutation in the GFAP gene.

Iwasaki Y, Saito Y, Mori K, Ito M, Mimuro M, Aiba I, Saito K, Mizuta I, Yoshida T, Nakagawa M, Yoshida M. Iwasaki Y, et al. Clin Neuropathol. 2015 Jul-Aug;34(4):207-14. doi: 10.5414/NP300806. Clin Neuropathol. 2015. PMID: 25828773

10

Adult-onset Alexander disease : report on a family.

Balbi P, Seri M, Ceccherini I, Uggetti C, Casale R, Fundarò C, Caroli F, Santoro L. Balbi P, et al. J Neurol. 2008 Jan;255(1):24-30. doi: 10.1007/s00415-007-0654-0. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004641

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