Daoud H - Search Results

1

Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.

Belzil VV, André-Guimont C, Atallah MR, Daoud H, Dupré N, Bouchard JP, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: daoud h. Neurobiol Aging. 2012 Aug;33(8):1845.e7-9. doi: 10.1016/j.neurobiolaging.2012.01.011. Epub 2012 Feb 22. Neurobiol Aging. 2012. PMID: 22361451

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

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.

4

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

5

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

6

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

7

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

8

Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.

Belzil VV, Daoud H, St-Onge J, Desjarlais A, Bouchard JP, Dupre N, Lacomblez L, Salachas F, Pradat PF, Meininger V, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: daoud h. Amyotroph Lateral Scler. 2011 Mar;12(2):113-7. doi: 10.3109/17482968.2010.536840. Epub 2011 Jan 24. Amyotroph Lateral Scler. 2011. PMID: 21261515

9

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.

Daoud H, Belzil V, Martins S, Sabbagh M, Provencher P, Lacomblez L, Meininger V, Camu W, Dupré N, Dion PA, Rouleau GA. Daoud H, et al. Arch Neurol. 2011 Jun;68(6):739-42. doi: 10.1001/archneurol.2011.111. Arch Neurol. 2011. PMID: 21670397

10

Exome sequencing reveals SPG11 mutations causing juvenile ALS.

Daoud H, Zhou S, Noreau A, Sabbagh M, Belzil V, Dionne-Laporte A, Tranchant C, Dion P, Rouleau GA. Daoud H, et al. Neurobiol Aging. 2012 Apr;33(4):839.e5-9. doi: 10.1016/j.neurobiolaging.2011.11.012. Epub 2011 Dec 10. Neurobiol Aging. 2012. PMID: 22154821

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