Vourc'h P - Search Results

1

Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions.

Codron P, Cassereau J, Vourc'h P, Veyrat-Durebex C, Blasco H, Kane S, Procaccio V, Letournel F, Verny C, Lenears G, Reynier P, Chevrollier A. Codron P, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):446-456. doi: 10.1080/21678421.2018.1431787. Epub 2018 Jan 31. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29382228

2

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Paubel A, Violette J, Amy M, Praline J, Meininger V, Camu W, Corcia P, Andres CR, Vourc'h P; French Amyotrophic Lateral Sclerosis (ALS) Study Group. Paubel A, et al. Arch Neurol. 2008 Oct;65(10):1333-6. doi: 10.1001/archneur.65.10.1333. Arch Neurol. 2008. PMID: 18852347

3

CADASIL and ALS: a link?

Praline J, Limousin N, Vourc'h P, Pallix M, Debiais S, Guennoc AM, Andres CR, Corcia P. Praline J, et al. Amyotroph Lateral Scler. 2010 Aug;11(4):399-401. doi: 10.1080/17482960903033153. Amyotroph Lateral Scler. 2010. PMID: 19488902

4

Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS.

Martin I, Vourc'h P, Mahé M, Thépault RA, Antar C, Védrine S, Praline J, Camu W, Andres CR, Corcia P; French ALS Study Group. Martin I, et al. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):432-5. doi: 10.3109/17482960802444972. Amyotroph Lateral Scler. 2009. PMID: 19922136

5

The importance of the SMN genes in the genetics of sporadic ALS.

Corcia P, Camu W, Praline J, Gordon PH, Vourch P, Andres C. Corcia P, et al. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):436-40. doi: 10.3109/17482960902759162. Amyotroph Lateral Scler. 2009. PMID: 19922137

6

Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees.

Praline J, Guennoc AM, Vourc'h P, De Toffol B, Corcia P. Praline J, et al. Amyotroph Lateral Scler. 2010;11(1-2):154-6. doi: 10.3109/17482960802483038. Amyotroph Lateral Scler. 2010. PMID: 20184517

7

[Chronic demyelinating polyneuropathy and B6 hypervitaminosis].

Castagnet S, Blasco H, Vourc'h P, Andres CR, Praline J. Castagnet S, et al. Rev Med Interne. 2010 Dec;31(12):e1-3. doi: 10.1016/j.revmed.2010.03.457. Epub 2010 Jun 2. Rev Med Interne. 2010. PMID: 20627481 French.

8

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.

Blasco H, Corcia P, Veyrat-Durebex C, Coutadeur C, Fournier C, Camu W, Gordon P, Praline J, Andres CR, Vourc'h P; French ALS Study Group. Blasco H, et al. Amyotroph Lateral Scler. 2011 May;12(3):210-4. doi: 10.3109/17482968.2010.522587. Epub 2010 Oct 11. Amyotroph Lateral Scler. 2011. PMID: 20932227

9

1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosis.

Blasco H, Corcia P, Moreau C, Veau S, Fournier C, Vourc'h P, Emond P, Gordon P, Pradat PF, Praline J, Devos D, Nadal-Desbarats L, Andres CR. Blasco H, et al. PLoS One. 2010 Oct 8;5(10):e13223. doi: 10.1371/journal.pone.0013223. PLoS One. 2010. PMID: 20949041 Free PMC article.

10

APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in men.

Praline J, Blasco H, Vourc'h P, Garrigue MA, Gordon PH, Camu W, Corcia P, Andres CR; French ALS Study Group. Praline J, et al. Eur J Neurol. 2011 Aug;18(8):1046-52. doi: 10.1111/j.1468-1331.2010.03330.x. Epub 2011 Jan 20. Eur J Neurol. 2011. PMID: 21251163

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