Rouleau G - Search Results

1

[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: rouleau g. 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.

2

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: rouleau g. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920

3

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: rouleau ga. 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.

4

Familial amyotrophic lateral sclerosis.

Hand CK, Rouleau GA. Hand CK, et al. Muscle Nerve. 2002 Feb;25(2):135-59. doi: 10.1002/mus.10001. Muscle Nerve. 2002. PMID: 11870681 Review.

5

Absence of mutations in the hypoxia response element of VEGF in ALS.

Gros-Louis F, Laurent S, Lopes AA, Khoris J, Meininger V, Camu W, Rouleau GA. Gros-Louis F, et al. Muscle Nerve. 2003 Dec;28(6):774-5. doi: 10.1002/mus.10498. Muscle Nerve. 2003. PMID: 14639597 No abstract available.

6

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. Arch Neurol. 2003 Dec;60(12):1768-71. doi: 10.1001/archneur.60.12.1768. Arch Neurol. 2003. PMID: 14676054

7

A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.

Gros-Louis F, Larivière R, Gowing G, Laurent S, Camu W, Bouchard JP, Meininger V, Rouleau GA, Julien JP. Gros-Louis F, et al. Among authors: rouleau ga. J Biol Chem. 2004 Oct 29;279(44):45951-6. doi: 10.1074/jbc.M408139200. Epub 2004 Aug 17. J Biol Chem. 2004. PMID: 15322088 Free article.

8

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

Valdmanis PN, Dupre N, Bouchard JP, Camu W, Salachas F, Meininger V, Strong M, Rouleau GA. Valdmanis PN, et al. Arch Neurol. 2007 Feb;64(2):240-5. doi: 10.1001/archneur.64.2.240. Arch Neurol. 2007. PMID: 17296840

9

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.

Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Vande Velde C, Bouchard JP, Lacomblez L, Pochigaeva K, Salachas F, Pradat PF, Camu W, Meininger V, Dupre N, Rouleau GA. Kabashi E, et al. Nat Genet. 2008 May;40(5):572-4. doi: 10.1038/ng.132. Epub 2008 Mar 30. Nat Genet. 2008. PMID: 18372902

10

Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.

Gros-Louis F, Andersen PM, Dupre N, Urushitani M, Dion P, Souchon F, D'Amour M, Camu W, Meininger V, Bouchard JP, Rouleau GA, Julien JP. Gros-Louis F, et al. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21777-82. doi: 10.1073/pnas.0902174106. Epub 2009 Dec 9. Proc Natl Acad Sci U S A. 2009. PMID: 20007371 Free PMC article.

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