Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

223 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Alexander disease.
Messing A, Brenner M, Feany MB, Nedergaard M, Goldman JE. Messing A, et al. Among authors: goldman je. J Neurosci. 2012 Apr 11;32(15):5017-23. doi: 10.1523/JNEUROSCI.5384-11.2012. J Neurosci. 2012. PMID: 22496548 Free PMC article. No abstract available.
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.
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.
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
GFAP and its role in Alexander disease.
Quinlan RA, Brenner M, Goldman JE, Messing A. Quinlan RA, et al. Among authors: goldman je. Exp Cell Res. 2007 Jun 10;313(10):2077-87. doi: 10.1016/j.yexcr.2007.04.004. Epub 2007 Apr 6. Exp Cell Res. 2007. PMID: 17498694 Free PMC article. Review.
223 results