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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

659 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
SOD1 mutation can mask C9orf72 abnormal expansion.
Corcia P, Blasco H, Besson G, Camdessanché JP, Pautot V, Beltran S, Couratier P, Andres C, Camu W, Vourc'h P. Corcia P, et al. Among authors: andres c. Eur J Neurol. 2017 Apr;24(4):e24. doi: 10.1111/ene.13257. Eur J Neurol. 2017. PMID: 28322003 No abstract available.
Genetics of amyotrophic lateral sclerosis.
Corcia P, Couratier P, Blasco H, Andres CR, Beltran S, Meininger V, Vourc'h P. Corcia P, et al. Among authors: andres cr. Rev Neurol (Paris). 2017 May;173(5):254-262. doi: 10.1016/j.neurol.2017.03.030. Epub 2017 Apr 25. Rev Neurol (Paris). 2017. PMID: 28449881 Review.
Respiratory onset in an ALS family with L144F SOD1 mutation.
Corcia P, Petiot P, Stevic Z, Vourc'h P, Morales R, Gordon PH, Pageot N, Andres C, Camu W. Corcia P, et al. Among authors: andres c. J Neurol Neurosurg Psychiatry. 2011 Jul;82(7):747-9. doi: 10.1136/jnnp.2009.197558. Epub 2010 Jun 20. J Neurol Neurosurg Psychiatry. 2011. PMID: 20562451
In ALS, a mutation could be worth two steps.
Corcia P, Blasco H, Beltran S, Andres C, Vourc'h P, Couratier P. Corcia P, et al. Among authors: andres c. Rev Neurol (Paris). 2018 Dec;174(10):669-670. doi: 10.1016/j.neurol.2018.11.001. Rev Neurol (Paris). 2018. PMID: 30501924 No abstract available.
SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.
Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Among authors: andres cr. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.
659 results