Camu W - Search Results

1

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

2

Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.

Camu W, Billiard M. Camu W, et al. J Neurol Sci. 1994 Jul;124 Suppl:88-9. doi: 10.1016/0022-510x(94)90189-9. J Neurol Sci. 1994. PMID: 7807154 No abstract available.

3

[Somatosensory evoked potentials in amyotrophic lateral sclerosis and primary lateral sclerosis].

Georgesco M, Salerno A, Carlander B, Léger JJ, Camu W, Billiard M, Cadilhac J. Georgesco M, et al. Among authors: camu w. Rev Neurol (Paris). 1994;150(4):292-8. Rev Neurol (Paris). 1994. PMID: 7863181 French.

4

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

5

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

6

[Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature].

Moulard B, Camu W, Malafosse A, Billiard M, Baldy-Moulinier M. Moulard B, et al. Among authors: camu w. Rev Neurol (Paris). 1997 Jun;153(5):314-24. Rev Neurol (Paris). 1997. PMID: 9296165 Review. French.

7

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

8

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

9

Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.

Al-Chalabi A, Andersen PM, Chioza B, Shaw C, Sham PC, Robberecht W, Matthijs G, Camu W, Marklund SL, Forsgren L, Rouleau G, Laing NG, Hurse PV, Siddique T, Leigh PN, Powell JF. Al-Chalabi A, et al. Among authors: camu w. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920

10

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

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