Camu W - Search Results

1

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

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

Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis.

Moulard B, Sefiani A, Laamri A, Malafosse A, Camu W. Moulard B, et al. Among authors: camu w. J Neurol Sci. 1996 Aug;139 Suppl:34-7. doi: 10.1016/0022-510x(96)00085-8. J Neurol Sci. 1996. PMID: 8899655

4

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.

5

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

6

Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.

Hand CK, Mayeux-Portas V, Khoris J, Briolotti V, Clavelou P, Camu W, Rouleau GA. Hand CK, et al. Among authors: camu w. Ann Neurol. 2001 Feb;49(2):267-71. doi: 10.1002/1531-8249(20010201)49:2<267::aid-ana51>3.0.co;2-d. Ann Neurol. 2001. PMID: 11220750

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

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

10

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.

Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, Bouchard JP, Camu W, Hayden MR, Rouleau GA. Hand CK, et al. Among authors: camu w. Arch Neurol. 2003 Dec;60(12):1768-71. doi: 10.1001/archneur.60.12.1768. Arch Neurol. 2003. PMID: 14676054

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