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Page 1
GFAP mutations in Alexander disease.
Li R, Messing A, Goldman JE, Brenner M. Li R, et al. Among authors: goldman je. Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):259-68. doi: 10.1016/s0736-5748(02)00019-9. Int J Dev Neurosci. 2002. PMID: 12175861 Review.
Alexander disease: new insights from genetics.
Messing A, Goldman JE, Johnson AB, Brenner M. Messing A, et al. Among authors: goldman je. J Neuropathol Exp Neurol. 2001 Jun;60(6):563-73. doi: 10.1093/jnen/60.6.563. J Neuropathol Exp Neurol. 2001. PMID: 11398833 Review.
Update on white matter genetic disorders.
Messing A, Brenner M, Johnson AB, Goldman JE. Messing A, et al. Among authors: goldman je. Pediatr Neurol. 2001 Oct;25(4):347-8; author reply 348. doi: 10.1016/s0887-8994(01)00340-x. Pediatr Neurol. 2001. PMID: 11704412 No abstract available.
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: goldman je. Ann Neurol. 2005 Mar;57(3):310-26. doi: 10.1002/ana.20406. Ann Neurol. 2005. PMID: 15732097
Propensity for paternal inheritance of de novo mutations in Alexander disease.
Li R, Johnson AB, Salomons GS, van der Knaap MS, Rodriguez D, Boespflug-Tanguy O, Gorospe JR, Goldman JE, Messing A, Brenner M. Li R, et al. Among authors: goldman je. Hum Genet. 2006 Mar;119(1-2):137-44. doi: 10.1007/s00439-005-0116-7. Epub 2005 Dec 20. Hum Genet. 2006. PMID: 16365765
218 results