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GFAP mutations, age at onset, and clinical subtypes in Alexander disease.
Prust M, Wang J, Morizono H, Messing A, Brenner M, Gordon E, Hartka T, Sokohl A, Schiffmann R, Gordish-Dressman H, Albin R, Amartino H, Brockman K, Dinopoulos A, Dotti MT, Fain D, Fernandez R, Ferreira J, Fleming J, Gill D, Griebel M, Heilstedt H, Kaplan P, Lewis D, Nakagawa M, Pedersen R, Reddy A, Sawaishi Y, Schneider M, Sherr E, Takiyama Y, Wakabayashi K, Gorospe JR, Vanderver A. Prust M, et al. Among authors: brenner m. Neurology. 2011 Sep 27;77(13):1287-94. doi: 10.1212/WNL.0b013e3182309f72. Epub 2011 Sep 14. Neurology. 2011. PMID: 21917775 Free PMC article.
Alexander disease: GFAP mutations unify young and old.
Messing A, Brenner M. Messing A, et al. Among authors: brenner m. Lancet Neurol. 2003 Feb;2(2):75. doi: 10.1016/s1474-4422(03)00301-6. Lancet Neurol. 2003. PMID: 12849260 No abstract available.
Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.
Gorospe JR, Naidu S, Johnson AB, Puri V, Raymond GV, Jenkins SD, Pedersen RC, Lewis D, Knowles P, Fernandez R, De Vivo D, van der Knaap MS, Messing A, Brenner M, Hoffman EP. Gorospe JR, et al. Among authors: brenner m. Neurology. 2002 May 28;58(10):1494-500. doi: 10.1212/wnl.58.10.1494. Neurology. 2002. PMID: 12034785
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. Among authors: brenner m. Ann Neurol. 2005 Mar;57(3):310-26. doi: 10.1002/ana.20406. Ann Neurol. 2005. PMID: 15732097
Unusual variants of Alexander's disease.
van der Knaap MS, Salomons GS, Li R, Franzoni E, Gutiérrez-Solana LG, Smit LM, Robinson R, Ferrie CD, Cree B, Reddy A, Thomas N, Banwell B, Barkhof F, Jakobs C, Johnson A, Messing A, Brenner M. van der Knaap MS, et al. Among authors: brenner m. Ann Neurol. 2005 Mar;57(3):327-38. doi: 10.1002/ana.20381. Ann Neurol. 2005. PMID: 15732098
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. Dotti MT, et al. Among authors: brenner m. J Neurol. 2009 Apr;256(4):679-82. doi: 10.1007/s00415-009-0147-4. Epub 2009 Apr 27. J Neurol. 2009. PMID: 19444543 Free PMC article. No abstract available.
GFAP at 50.
Messing A, Brenner M. Messing A, et al. Among authors: brenner m. ASN Neuro. 2020 Jan-Dec;12:1759091420949680. doi: 10.1177/1759091420949680. ASN Neuro. 2020. PMID: 32811163 Free PMC article. Review.
Regulation of GFAP Expression.
Brenner M, Messing A. Brenner M, et al. ASN Neuro. 2021 Jan-Dec;13:1759091420981206. doi: 10.1177/1759091420981206. ASN Neuro. 2021. PMID: 33601918 Free PMC article. Review.
2,209 results