Ouazzani R - Search Results

1

[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.

2

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

3

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

4

[Acute Guillain-Barré-like polyradiculoneuritis revealing acute systemic lupus erythematosus: two case studies and review of the literature].

Aït Benhaddou E, Birouk N, El Alaoui-Faris M, Mzalek-Tazi Z, Aïdi S, Belaïdi H, Kably B, Ouazzani R, Chkili T. Aït Benhaddou E, et al. Among authors: ouazzani r. Rev Neurol (Paris). 2003 Mar;159(3):300-6. Rev Neurol (Paris). 2003. PMID: 12703046 French.

5

[T-cell lymphoma revealed by a mononeuritis multiplex: case report and review of literature].

Rahmani M, Birouk N, Amarti A, Loukili Idrissi A, Marnissi F, Belaidi H, El Alaoui Faris M, Benchekroun S, Ouazzani R. Rahmani M, et al. Among authors: ouazzani r. Rev Neurol (Paris). 2007 Apr;163(4):462-70. doi: 10.1016/s0035-3787(07)90422-1. Rev Neurol (Paris). 2007. PMID: 17452948 French.

6

[Isaacs syndrome: clinical remission after methylprednisolone bolus].

Elalaoui-Faris M, Ouahabi H, Slassi I, Medejel A, Ouazzani R, Saidi A, Miri A, Alaoui I, Chkili T. Elalaoui-Faris M, et al. Among authors: ouazzani r. Rev Neurol (Paris). 1993;149(6-7):426-7. Rev Neurol (Paris). 1993. PMID: 8303166 French. No abstract available.

7

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

8

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

9

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

10

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

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

40 results

Search Page

Filters