Camu W - Search Results

1

Amyotrophic lateral sclerosis: a hormonal condition?

Blasco H, Guennoc AM, Veyrat-Durebex C, Gordon PH, Andres CR, Camu W, Corcia P. Blasco H, et al. Among authors: camu w. Amyotroph Lateral Scler. 2012 Oct;13(6):585-8. doi: 10.3109/17482968.2012.706303. Epub 2012 Aug 8. Amyotroph Lateral Scler. 2012. PMID: 22873563 Review.

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

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

5

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

6

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

7

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

8

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

9

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.

Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Among authors: camu w. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.

10

[What is the role of the genetic survey in amyotrophic lateral sclerosis?].

Camu W. Camu W. Rev Neurol (Paris). 2006 Jun;162 Spec No 2:4S91-4S95. Rev Neurol (Paris). 2006. PMID: 17128094 French.

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