Vourc'h P - Search Results

1

PET Study of Microglial Activation in Kleine-Levin Syndrome.

Barateau L, Krache A, Da Costa A, Lecendreux M, Chenini S, Arlicot N, Vourc'h P, Alonso M, Salabert AS, Beziat S, Jaussent I, Mariano-Goulart D, Payoux P, Dauvilliers Y. Barateau L, et al. Among authors: vourc h p. Neurol Neuroimmunol Neuroinflamm. 2024 Jul;11(4):e200263. doi: 10.1212/NXI.0000000000200263. Epub 2024 Jun 17. Neurol Neuroimmunol Neuroinflamm. 2024. PMID: 38885456 Free PMC article.

2

Evaluation of arterial blood gas parameters as prognostic markers in amyotrophic lateral sclerosis.

Alarcan H, Cotet C, Lépine N, Morel J, Vourc'h P, Andres C, Corcia P, Blasco H. Alarcan H, et al. Eur J Neurol. 2023 Jun;30(6):1611-1618. doi: 10.1111/ene.15779. Epub 2023 Mar 23. Eur J Neurol. 2023. PMID: 36906908

3

The debated toxic role of aggregated TDP-43 in amyotrophic lateral sclerosis: a resolution in sight?

Hergesheimer RC, Chami AA, de Assis DR, Vourc'h P, Andres CR, Corcia P, Lanznaster D, Blasco H. Hergesheimer RC, et al. Brain. 2019 May 1;142(5):1176-1194. doi: 10.1093/brain/awz078. Brain. 2019. PMID: 30938443 Free PMC article. Review.

4

Time for optimism in amyotrophic lateral sclerosis.

Corcia P, Lunetta C, Vourc'h P, Pradat PF, Blasco H. Corcia P, et al. Eur J Neurol. 2023 May;30(5):1459-1464. doi: 10.1111/ene.15738. Epub 2023 Feb 23. Eur J Neurol. 2023. PMID: 36773012 Review.

5

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.

6

Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: Supplementary evidence for a continuum.

Corcia P, Lunetta C, Couratier P, Vourc'h P, Gromicho M, Desnuelle C, Soriani MH, Pinto S, de Carvalho M. Corcia P, et al. Eur J Neurol. 2021 Aug;28(8):2780-2783. doi: 10.1111/ene.14960. Epub 2021 Jun 23. Eur J Neurol. 2021. PMID: 34110677

7

Comparison between PFN1 and SOD1 mutations in amyotrophic lateral sclerosis.

Corcia P, Lejeune P, Vourc'h P, Beltran S, Piegay AS, Blasco H, Meininger V. Corcia P, et al. Eur J Neurol. 2023 Feb;30(2):552-554. doi: 10.1111/ene.15583. Epub 2022 Oct 18. Eur J Neurol. 2023. PMID: 36176198 Review.

8

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

9

Aβ1-42 and Tau as Potential Biomarkers for Diagnosis and Prognosis of Amyotrophic Lateral Sclerosis.

Lanznaster D, Hergesheimer RC, Bakkouche SE, Beltran S, Vourc'h P, Andres CR, Dufour-Rainfray D, Corcia P, Blasco H. Lanznaster D, et al. Int J Mol Sci. 2020 Apr 21;21(8):2911. doi: 10.3390/ijms21082911. Int J Mol Sci. 2020. PMID: 32326346 Free PMC article.

10

Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients.

Alarcan H, Vourc'h P, Berton L, Benz-De Bretagne I, Piver E, Andres CR, Corcia P, Veyrat-Durebex C, Blasco H. Alarcan H, et al. Int J Mol Sci. 2023 Jul 7;24(13):11196. doi: 10.3390/ijms241311196. Int J Mol Sci. 2023. PMID: 37446372 Free PMC article.

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