Camu W - 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: camu w. 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

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: camu w. Ann Neurol. 1998 May;43(5):640-4. doi: 10.1002/ana.410430513. Ann Neurol. 1998. PMID: 9585359

3

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: camu w. Can J Neurol Sci. 1998 Aug;25(3):192-6. doi: 10.1017/s0317167100034004. Can J Neurol Sci. 1998. PMID: 9706719

4

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. J Neurol Sci. 1999 Jun;165 Suppl 1:S21-6. doi: 10.1016/s0022-510x(99)00022-2. J Neurol Sci. 1999. PMID: 10448977

5

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: camu w. Arch Dermatol. 2000 Apr;136(4):521-4. doi: 10.1001/archderm.136.4.521. Arch Dermatol. 2000. PMID: 10768651 Review.

6

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

7

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.

Hand CK, Khoris J, Salachas F, Gros-Louis F, Lopes AA, Mayeux-Portas V, Brewer CG, Brown RH Jr, Meininger V, Camu W, Rouleau GA. Hand CK, et al. Among authors: camu w. Am J Hum Genet. 2002 Jan;70(1):251-6. doi: 10.1086/337945. Epub 2001 Nov 9. Am J Hum Genet. 2002. PMID: 11706389 Free PMC article.

8

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis.

Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Müh JP, Camu W, Andres C; French ALS Research Group. Amyotrophic Lateral Sclerosis. Corcia P, et al. Among authors: camu w. Ann Neurol. 2002 Feb;51(2):243-6. doi: 10.1002/ana.10104. Ann Neurol. 2002. PMID: 11835381

9

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.

Corcia P, Khoris J, Couratier P, Mayeux-Portas V, Bieth E, De Toffol B, Autret A, Müh JP, Andres C, Camu W. Corcia P, et al. Among authors: camu w. Neurology. 2002 Nov 12;59(9):1464-6. doi: 10.1212/01.wnl.0000032500.73621.c5. Neurology. 2002. PMID: 12427909

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

248 results

Search Page