Similar articles for PMID: 12975300

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1

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

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

An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.

Asahina N, Okamoto T, Sudo A, Kanazawa N, Tsujino S, Saitoh S. Asahina N, et al. Brain Dev. 2006 Mar;28(2):131-3. doi: 10.1016/j.braindev.2005.05.004. Epub 2005 Sep 15. Brain Dev. 2006. PMID: 16168593 Free article.

4

Dominantly-inherited adult-onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene.

Thyagarajan D, Chataway T, Li R, Gai WP, Brenner M. Thyagarajan D, et al. Mov Disord. 2004 Oct;19(10):1244-8. doi: 10.1002/mds.20161. Mov Disord. 2004. PMID: 15390001

5

Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

van der Knaap MS, Ramesh V, Schiffmann R, Blaser S, Kyllerman M, Gholkar A, Ellison DW, van der Voorn JP, van Dooren SJ, Jakobs C, Barkhof F, Salomons GS. van der Knaap MS, et al. Neurology. 2006 Feb 28;66(4):494-8. doi: 10.1212/01.wnl.0000198770.80743.37. Neurology. 2006. PMID: 16505300

6

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. Li R, et al. Ann Neurol. 2005 Mar;57(3):310-26. doi: 10.1002/ana.20406. Ann Neurol. 2005. PMID: 15732097

7

Clinical and genetic study in Chinese patients with Alexander disease.

Ye Wu, Qiang Gu, Jingmin Wang, Yanling Yang, Xiru Wu, Yuwu Jiang. Ye Wu, et al. J Child Neurol. 2008 Feb;23(2):173-7. doi: 10.1177/0883073807308691. Epub 2007 Dec 13. J Child Neurol. 2008. PMID: 18079314

8

Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.

Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T. Murakami N, et al. Pediatr Neurol. 2008 Jan;38(1):50-2. doi: 10.1016/j.pediatrneurol.2007.08.017. Pediatr Neurol. 2008. PMID: 18054694

9

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

10

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. Jefferson RJ, et al. Dev Med Child Neurol. 2010 Dec;52(12):1160-3. doi: 10.1111/j.1469-8749.2010.03784.x. Epub 2010 Oct 21. Dev Med Child Neurol. 2010. PMID: 20964669 Free article.

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