Vourc'h P - Search Results

1

Corcia P, Lumbroso S, Cazeneuve C, Mouzat K, Camu W, Vourc'h P; on Behalf the FILSLAN network. Corcia P, et al. Rev Neurol (Paris). 2020 Mar;176(3):166-169. doi: 10.1016/j.neurol.2019.07.027. Epub 2020 Jan 10. Rev Neurol (Paris). 2020. PMID: 31932031

2

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. 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.

3

[Genetics of motor neuron disorders].

Corcia P, Praline J, Vourc'h P, Andres C. Corcia P, et al. Rev Neurol (Paris). 2008 Feb;164(2):115-30. doi: 10.1016/j.neurol.2007.10.002. Epub 2008 Feb 20. Rev Neurol (Paris). 2008. PMID: 18358870 Review. French.

4

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

5

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

6

Effect of the oligodendrocyte myelin glycoprotein (OMgp) on the expansion and neuronal differentiation of rat neural stem cells.

Martin I, Andres CR, Védrine S, Tabagh R, Michelle C, Jourdan ML, Heuze-Vourc'h N, Corcia P, Duittoz A, Vourc'h P. Martin I, et al. Brain Res. 2009 Aug 11;1284:22-30. doi: 10.1016/j.brainres.2009.05.070. Epub 2009 Jun 6. Brain Res. 2009. PMID: 19501059

7

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

8

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

9

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

10

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. 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

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