Camu W - Search Results

1

A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALS.

Blasco H, Bernard-Marissal N, Vourc'h P, Guettard YO, Sunyach C, Augereau O, Khederchah J, Mouzat K, Antar C, Gordon PH, Veyrat-Durebex C, Besson G, Andersen PM, Salachas F, Meininger V, Camu W, Pettmann B, Andres CR, Corcia P; French ALS Study Group. Blasco H, et al. Among authors: camu w. Hum Mutat. 2013 Jul;34(7):953-60. doi: 10.1002/humu.22329. Epub 2013 May 28. Hum Mutat. 2013. PMID: 23568759

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

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.

7

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

8

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

9

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

10

N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.

Mayeux V, Corcia P, Besson G, Jafari-Schluep HF, Briolotti V, Camu W. Mayeux V, et al. Among authors: camu w. Ann Neurol. 2003 Jun;53(6):815-8. doi: 10.1002/ana.10605. Ann Neurol. 2003. PMID: 12783432

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