Daoud H - Search Results

1

C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia.

Daoud H, Suhail H, Sabbagh M, Belzil V, Szuto A, Dionne-Laporte A, Khoris J, Camu W, Salachas F, Meininger V, Mathieu J, Strong M, Dion PA, Rouleau GA. Daoud H, et al. Arch Neurol. 2012 Sep;69(9):1159-63. doi: 10.1001/archneurol.2012.377. Arch Neurol. 2012. PMID: 22964911

2

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

Daoud H, Valdmanis PN, Kabashi E, Dion P, Dupré N, Camu W, Meininger V, Rouleau GA. Daoud H, et al. J Med Genet. 2009 Feb;46(2):112-4. doi: 10.1136/jmg.2008.062463. Epub 2008 Oct 17. J Med Genet. 2009. PMID: 18931000

3

Mutations in FUS cause FALS and SALS in French and French Canadian populations.

Belzil VV, Valdmanis PN, Dion PA, Daoud H, Kabashi E, Noreau A, Gauthier J; S2D team; Hince P, Desjarlais A, Bouchard JP, Lacomblez L, Salachas F, Pradat PF, Camu W, Meininger V, Dupré N, Rouleau GA. Belzil VV, et al. Among authors: daoud h. Neurology. 2009 Oct 13;73(15):1176-9. doi: 10.1212/WNL.0b013e3181bbfeef. Epub 2009 Sep 9. Neurology. 2009. PMID: 19741216 Free PMC article.

4

Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations.

Corcia P, Valdmanis P, Millecamps S, Lionnet C, Blasco H, Mouzat K, Daoud H, Belzil V, Morales R, Pageot N, Danel-Brunaud V, Vandenberghe N, Pradat PF, Couratier P, Salachas F, Lumbroso S, Rouleau GA, Meininger V, Camu W. Corcia P, et al. Among authors: daoud h. Neurology. 2012 May 8;78(19):1519-26. doi: 10.1212/WNL.0b013e3182553c88. Epub 2012 Apr 25. Neurology. 2012. PMID: 22539580

5

Recent advances in the genetics of amyotrophic lateral sclerosis.

Valdmanis PN, Daoud H, Dion PA, Rouleau GA. Valdmanis PN, et al. Among authors: daoud h. Curr Neurol Neurosci Rep. 2009 May;9(3):198-205. doi: 10.1007/s11910-009-0030-9. Curr Neurol Neurosci Rep. 2009. PMID: 19348708 Review.

6

Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis.

Daoud H, Valdmanis PN, Dion PA, Rouleau GA. Daoud H, et al. Amyotroph Lateral Scler. 2010 Aug;11(4):389-91. doi: 10.3109/17482960903358857. Amyotroph Lateral Scler. 2010. PMID: 20001489

7

Analysis of the UNC13A gene as a risk factor for sporadic amyotrophic lateral sclerosis.

Daoud H, Belzil V, Desjarlais A, Camu W, Dion PA, Rouleau GA. Daoud H, et al. Arch Neurol. 2010 Apr;67(4):516-7. doi: 10.1001/archneurol.2010.46. Arch Neurol. 2010. PMID: 20385924 No abstract available.

8

Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.

Belzil VV, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: daoud h. Neurobiol Aging. 2011 Mar;32(3):555.e13-4. doi: 10.1016/j.neurobiolaging.2010.10.001. Epub 2010 Nov 11. Neurobiol Aging. 2011. PMID: 21074290

9

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.

Belzil VV, St-Onge J, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: daoud h. J Hum Genet. 2011 Mar;56(3):247-9. doi: 10.1038/jhg.2010.162. Epub 2010 Dec 16. J Hum Genet. 2011. PMID: 21160488

10

Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

Daoud H, Valdmanis PN, Gros-Louis F, Belzil V, Spiegelman D, Henrion E, Diallo O, Desjarlais A, Gauthier J, Camu W, Dion PA, Rouleau GA. Daoud H, et al. Arch Neurol. 2011 May;68(5):587-93. doi: 10.1001/archneurol.2010.351. Epub 2011 Jan 10. Arch Neurol. 2011. PMID: 21220648

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