Salachas F - Search Results

1

Screening of OPTN in French familial amyotrophic lateral sclerosis.

Millecamps S, Boillée S, Chabrol E, Camu W, Cazeneuve C, Salachas F, Pradat PF, Danel-Brunaud V, Vandenberghe N, Corcia P, Le Forestier N, Lacomblez L, Bruneteau G, Seilhean D, Brice A, Feingold J, Meininger V, LeGuern E. Millecamps S, et al. Among authors: salachas f. Neurobiol Aging. 2011 Mar;32(3):557.e11-3. doi: 10.1016/j.neurobiolaging.2010.11.005. Epub 2011 Jan 8. Neurobiol Aging. 2011. PMID: 21220178

2

[Acoustic parameters of voice and speech in a case of bulbar amyotrophic lateral sclerosis].

Crevier-Buchman L, Laccourreye O, Meininger V, Salachas F, Brihaye S, Brasnu D. Crevier-Buchman L, et al. Among authors: salachas f. Ann Otolaryngol Chir Cervicofac. 1995;112(4):169-73. Ann Otolaryngol Chir Cervicofac. 1995. PMID: 7574245 French.

3

Natural history of amyotrophic lateral sclerosis. A discussion.

Meininger V, Bensimon G, Lacomblez L, Salachas F. Meininger V, et al. Among authors: salachas f. Adv Neurol. 1995;68:199-207. Adv Neurol. 1995. PMID: 8787230 Review. No abstract available.

4

Influence of neck muscles on mouth pressure response to cervical magnetic stimulation.

Attali V, Mehiri S, Straus C, Salachas F, Arnulf I, Meininger V, Derenne JP, Similowski T. Attali V, et al. Among authors: salachas f. Am J Respir Crit Care Med. 1997 Aug;156(2 Pt 1):509-14. doi: 10.1164/ajrccm.156.2.9612053. Am J Respir Crit Care Med. 1997. PMID: 9279232

5

Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease.

Moulard B, Salachas F, Chassande B, Briolotti V, Meininger V, Malafosse A, Camu W. Moulard B, et al. Among authors: salachas f. Ann Neurol. 1998 May;43(5):640-4. doi: 10.1002/ana.410430513. Ann Neurol. 1998. PMID: 9585359

6

Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis.

Boukaftane Y, Khoris J, Moulard B, Salachas F, Meininger V, Malafosse A, Camu W, Rouleau GA. Boukaftane Y, et al. Among authors: salachas f. Can J Neurol Sci. 1998 Aug;25(3):192-6. doi: 10.1017/s0317167100034004. Can J Neurol Sci. 1998. PMID: 9706719

7

Genetics of familial ALS and consequences for diagnosis. French ALS Research Group.

Camu W, Khoris J, Moulard B, Salachas F, Briolotti V, Rouleau GA, Meininger V. Camu W, et al. Among authors: salachas f. J Neurol Sci. 1999 Jun;165 Suppl 1:S21-6. doi: 10.1016/s0022-510x(99)00022-2. J Neurol Sci. 1999. PMID: 10448977

8

Diaphragmatic dysfunction and dyspnoea in amyotrophic lateral sclerosis.

Similowski T, Attali V, Bensimon G, Salachas F, Mehiri S, Arnulf I, Lacomblez L, Zelter M, Meininger V, Derenne JP. Similowski T, et al. Among authors: salachas f. Eur Respir J. 2000 Feb;15(2):332-7. doi: 10.1034/j.1399-3003.2000.15b19.x. Eur Respir J. 2000. PMID: 10706501 Free article.

9

Sleep disorders and diaphragmatic function in patients with amyotrophic lateral sclerosis.

Arnulf I, Similowski T, Salachas F, Garma L, Mehiri S, Attali V, Behin-Bellhesen V, Meininger V, Derenne JP. Arnulf I, et al. Among authors: salachas f. Am J Respir Crit Care Med. 2000 Mar;161(3 Pt 1):849-56. doi: 10.1164/ajrccm.161.3.9805008. Am J Respir Crit Care Med. 2000. PMID: 10712332

10

Bullous pemphigoid and amyotrophic lateral sclerosis: a new clue for understanding the bullous disease?

Chosidow O, Doppler V, Bensimon G, Joly P, Salachas F, Lacomblez L, Prost C, Camu W, Francès C, Herson S, Meininger V. Chosidow O, et al. Among authors: salachas f. Arch Dermatol. 2000 Apr;136(4):521-4. doi: 10.1001/archderm.136.4.521. Arch Dermatol. 2000. PMID: 10768651 Review.

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