Ceftriaxone for Alexander’s Disease: A Four-Year Follow-Up
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/8904_2012_180
Reference22 articles.
1. Bachetti T, Di Zanni E, Balbi P et al (2010) In vitro treatments with ceftriaxone promote elimination of mutant glial fibrillary acidic protein and transcription down-regulation. Exp Cell Res 316:2152–2165
2. Balbi P, Salvini S, Fundarò C et al (2010) The clinical spectrum of late-onset Alexander disease: a systematic literature review. J Neurol 257:1955–1962
3. Brenner M, Johnson AB, Boesflug-Tanguy O, Rodriguez D, Goldman JE, Messing A (2001) Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet 27:117–120
4. Cho W, Brenner M, Peters N, Messing A (2010) Drug screening to identify suppressors of GFAP expression. Hum Mol Genet 19:3169–3178
5. Der Perng M, Su M, Wen SF et al (2006) The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and tha association of αB-crystallin and HSP27. Am J Hum Genet 79:197–213
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