Camu W - Search Results

1

Serum neurofilament light chain cut-off definition for clinical diagnosis and prognosis of amyotrophic lateral sclerosis.

Brousse M, Delaby C, De La Cruz E, Kuhle J, Benkert P, Mondesert E, Ginestet N, Hirtz C, Camu W, Lehmann S, Esselin F. Brousse M, et al. Among authors: camu w. Eur J Neurol. 2023 Jul;30(7):1919-1927. doi: 10.1111/ene.15813. Epub 2023 Apr 19. Eur J Neurol. 2023. PMID: 37029777

2

Conjugal amyotrophic lateral sclerosis: a report on two couples from southern France.

Camu W, Cadilhac J, Billiard M. Camu W, et al. Neurology. 1994 Mar;44(3 Pt 1):547-8. doi: 10.1212/wnl.44.3_part_1.547. Neurology. 1994. PMID: 8145930

3

Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country.

Khoris J, Moulard B, Briolotti V, Hayer M, Durieux A, Clavelou P, Malafosse A, Rouleau GA, Camu W. Khoris J, et al. Among authors: camu w. Eur J Neurol. 2000 Mar;7(2):207-11. doi: 10.1046/j.1468-1331.2000.00028.x. Eur J Neurol. 2000. PMID: 10809943

4

A clustering of conjugal amyotrophic lateral sclerosis in southeastern France.

Corcia P, Jafari-Schluep HF, Lardillier D, Mazyad H, Giraud P, Clavelou P, Pouget J, Camu W. Corcia P, et al. Among authors: camu w. Arch Neurol. 2003 Apr;60(4):553-7. doi: 10.1001/archneur.60.4.553. Arch Neurol. 2003. PMID: 12707069

5

Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study.

Gil J, Funalot B, Verschueren A, Danel-Brunaud V, Camu W, Vandenberghe N, Desnuelle C, Guy N, Camdessanche JP, Cintas P, Carluer L, Pittion S, Nicolas G, Corcia P, Fleury MC, Maugras C, Besson G, Le Masson G, Couratier P. Gil J, et al. Among authors: camu w. Eur J Neurol. 2008 Nov;15(11):1245-51. doi: 10.1111/j.1468-1331.2008.02307.x. Eur J Neurol. 2008. PMID: 18973614

6

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. Among authors: camu w. 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

7

Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations.

Corcia P, Valdmanis P, Millecamps S, Lionnet C, Blasco H, Mouzat K, Daoud H, Belzil V, Morales R, Pageot N, Danel-Brunaud V, Vandenberghe N, Pradat PF, Couratier P, Salachas F, Lumbroso S, Rouleau GA, Meininger V, Camu W. Corcia P, et al. Among authors: camu w. Neurology. 2012 May 8;78(19):1519-26. doi: 10.1212/WNL.0b013e3182553c88. Epub 2012 Apr 25. Neurology. 2012. PMID: 22539580

8

A phase II-III trial of olesoxime in subjects with amyotrophic lateral sclerosis.

Lenglet T, Lacomblez L, Abitbol JL, Ludolph A, Mora JS, Robberecht W, Shaw PJ, Pruss RM, Cuvier V, Meininger V; Mitotarget study group. Lenglet T, et al. Eur J Neurol. 2014 Mar;21(3):529-36. doi: 10.1111/ene.12344. Epub 2014 Jan 21. Eur J Neurol. 2014. PMID: 24447620 Clinical Trial.

9

The Use of Peripherally Inserted Central Catheter in Amyotrophic Lateral Sclerosis Patients at a Later Stage.

Juntas-Morales R, Pageot N, Alphandéry S, Camu W. Juntas-Morales R, et al. Among authors: camu w. Eur Neurol. 2017;77(1-2):87-90. doi: 10.1159/000454858. Epub 2016 Dec 16. Eur Neurol. 2017. PMID: 27978519

10

Serum neurofilament light chain at time of diagnosis is an independent prognostic factor of survival in amyotrophic lateral sclerosis.

Thouvenot E, Demattei C, Lehmann S, Maceski-Maleska A, Hirtz C, Juntas-Morales R, Pageot N, Esselin F, Alphandéry S, Vincent T, Camu W. Thouvenot E, et al. Among authors: camu w. Eur J Neurol. 2020 Feb;27(2):251-257. doi: 10.1111/ene.14063. Epub 2019 Sep 18. Eur J Neurol. 2020. PMID: 31437330

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