Ouazzani R - Search Results

1

Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene.

Birouk N, Azzedine H, Dubourg O, Muriel MP, Benomar A, Hamadouche T, Maisonobe T, Ouazzani R, Brice A, Yahyaoui M, Chkili T, Le Guern E. Birouk N, et al. Among authors: ouazzani r. Arch Neurol. 2003 Apr;60(4):598-604. doi: 10.1001/archneur.60.4.598. Arch Neurol. 2003. PMID: 12707075

2

Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.

Bouhouche A, Benomar A, Bouslam N, Ouazzani R, Chkili T, Yahyaoui M. Bouhouche A, et al. Among authors: ouazzani r. Eur J Hum Genet. 2006 Feb;14(2):249-52. doi: 10.1038/sj.ejhg.5201537. Eur J Hum Genet. 2006. PMID: 16333315

3

Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.

Bouhouche A, Birouk N, Azzedine H, Benomar A, Durosier G, Ente D, Muriel MP, Ruberg M, Slassi I, Yahyaoui M, Dubourg O, Ouazzani R, LeGuern E. Bouhouche A, et al. Among authors: ouazzani r. Brain. 2007 Apr;130(Pt 4):1062-75. doi: 10.1093/brain/awm014. Epub 2007 Mar 8. Brain. 2007. PMID: 17347251

4

A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families.

Bouhouche A, Birouk N, Benomar A, Ouazzani R, Chkili T, Yahyaoui M. Bouhouche A, et al. Among authors: ouazzani r. Can J Neurol Sci. 2007 Nov;34(4):421-6. doi: 10.1017/s0317167100007290. Can J Neurol Sci. 2007. PMID: 18062449

5

High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.

Bouhouche A, Benomar A, Birouk N, Bouslam N, Ouazzani R, Yahyaoui M, Chkili T. Bouhouche A, et al. Among authors: ouazzani r. J Neurol. 2003 Oct;250(10):1209-13. doi: 10.1007/s00415-003-0186-1. J Neurol. 2003. PMID: 14586604

6

Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.

Baulac S, Lenk GM, Dufresnois B, Ouled Amar Bencheikh B, Couarch P, Renard J, Larson PA, Ferguson CJ, Noé E, Poirier K, Hubans C, Ferreira S, Guerrini R, Ouazzani R, El Hachimi KH, Meisler MH, Leguern E. Baulac S, et al. Among authors: ouazzani r. Neurology. 2014 Mar 25;82(12):1068-75. doi: 10.1212/WNL.0000000000000241. Epub 2014 Mar 5. Neurology. 2014. PMID: 24598713 Free PMC article.

7

[Late discovery of Lafora disease: a family study].

Messouak O, Yahyaoui M, Benabdeljalil M, Benomar A, Ouazzani R, Amarti A, Saidi A, Chkili T. Messouak O, et al. Among authors: ouazzani r. Rev Neurol (Paris). 2002 Jan;158(1):74-6. Rev Neurol (Paris). 2002. PMID: 11938326 French.

8

Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.

Benomar A, Yahyaoui M, Meggouh F, Bouhouche A, Boutchich M, Bouslam N, Zaim A, Schmitt M, Belaidi H, Ouazzani R, Chkili T, Koenig M. Benomar A, et al. Among authors: ouazzani r. J Neurol Sci. 2002 Jun 15;198(1-2):25-9. doi: 10.1016/s0022-510x(02)00057-6. J Neurol Sci. 2002. PMID: 12039660

9

A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.

Ben Cheikh BO, Baulac S, Lahjouji F, Bouhouche A, Couarch P, Khalili N, Regragui W, Lehericy S, Ruberg M, Benomar A, Heath S, Chkili T, Yahyaoui M, Jiddane M, Ouazzani R, LeGuern E. Ben Cheikh BO, et al. Among authors: ouazzani r. Neurogenetics. 2009 Feb;10(1):35-42. doi: 10.1007/s10048-008-0143-3. Epub 2008 Aug 29. Neurogenetics. 2009. PMID: 18758830

10

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B. Gan-Or Z, et al. Among authors: ouazzani r. Am J Hum Genet. 2016 May 5;98(5):1038-1046. doi: 10.1016/j.ajhg.2016.04.002. Am J Hum Genet. 2016. PMID: 27153400 Free PMC article.

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