Camu W - Search Results

1

Compound heterozygous P67S/D91A SOD1 mutations in an ALS family with apparently sporadic case.

De La Cruz E, Guissart C, Esselin F, Polge A, Pageot N, Taieb G, Lumbroso S, Camu W, Mouzat K. De La Cruz E, et al. Among authors: camu w. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Aug;23(5-6):458-461. doi: 10.1080/21678421.2021.1990344. Epub 2021 Oct 20. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34668453

2

[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.

3

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

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

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

6

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

7

[Superoxyde dismutase 1 gene abnormalities in familial amyotrophic lateral sclerosis: phenotype/genotype correlations. The French experience and review of the literature].

Jafari-Schluep HF, Khoris J, Mayeux-Portas V, Hand C, Rouleau G, Camu W; Groupe Français d'Etude des Maladies du Motoneurone. Jafari-Schluep HF, et al. Among authors: camu w. Rev Neurol (Paris). 2004 Jan;160(1):44-50. doi: 10.1016/s0035-3787(04)70846-2. Rev Neurol (Paris). 2004. PMID: 14978393 Review. French.

8

[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.

9

Association study of the ubiquitin conjugating enzyme gene UBE2H in sporadic ALS.

Martin I, Vourc'h P, Mahé M, Thépault RA, Antar C, Védrine S, Praline J, Camu W, Andres CR, Corcia P; French ALS Study Group. Martin I, et al. Among authors: camu w. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):432-5. doi: 10.3109/17482960802444972. Amyotroph Lateral Scler. 2009. PMID: 19922136

10

The importance of the SMN genes in the genetics of sporadic ALS.

Corcia P, Camu W, Praline J, Gordon PH, Vourch P, Andres C. Corcia P, et al. Among authors: camu w. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):436-40. doi: 10.3109/17482960902759162. Amyotroph Lateral Scler. 2009. PMID: 19922137

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

257 results

Search Page

Filters