Bouhouche A - Search Results

1

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

Bouslam N, Benomar A, Azzedine H, Bouhouche A, Namekawa M, Klebe S, Charon C, Durr A, Ruberg M, Brice A, Yahyaoui M, Stevanin G. Bouslam N, et al. Among authors: bouhouche a. Ann Neurol. 2005 Apr;57(4):567-71. doi: 10.1002/ana.20416. Ann Neurol. 2005. PMID: 15786464

2

A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Bouhouche A, Benomar A, Birouk N, Mularoni A, Meggouh F, Tassin J, Grid D, Vandenberghe A, Yahyaoui M, Chkili T, Brice A, LeGuern E. Bouhouche A, et al. Am J Hum Genet. 1999 Sep;65(3):722-7. doi: 10.1086/302542. Am J Hum Genet. 1999. PMID: 10441578 Free PMC article.

3

The autosomal recessive form of CMT disease linked to 5q31-q33.

Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, Leguern E. Guilbot A, et al. Among authors: bouhouche a. Ann N Y Acad Sci. 1999 Sep 14;883:56-9. Ann N Y Acad Sci. 1999. PMID: 10586230 No abstract available.

4

The autosomal recessive form of CMT disease linked to 5q31-q33.

Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, LeGuern E. Guilbot A, et al. Among authors: bouhouche a. Ann N Y Acad Sci. 1999 Sep 14;883:453-6. Ann N Y Acad Sci. 1999. PMID: 10586271 No abstract available.

5

Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1.

Guilbot A, Ravisé N, Bouhouche A, Coullin P, Birouk N, Maisonobe T, Kuntzer T, Vial C, Grid D, Brice A, LeGuern E. Guilbot A, et al. Among authors: bouhouche a. Eur J Hum Genet. 1999 Dec;7(8):849-59. doi: 10.1038/sj.ejhg.5200382. Eur J Hum Genet. 1999. PMID: 10602360

6

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: bouhouche a. 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

7

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.

Azzedine H, Bolino A, Taïeb T, Birouk N, Di Duca M, Bouhouche A, Benamou S, Mrabet A, Hammadouche T, Chkili T, Gouider R, Ravazzolo R, Brice A, Laporte J, LeGuern E. Azzedine H, et al. Among authors: bouhouche a. Am J Hum Genet. 2003 May;72(5):1141-53. doi: 10.1086/375034. Epub 2003 Apr 8. Am J Hum Genet. 2003. PMID: 12687498 Free PMC article.

8

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. J Neurol. 2003 Oct;250(10):1209-13. doi: 10.1007/s00415-003-0186-1. J Neurol. 2003. PMID: 14586604

9

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. Eur J Hum Genet. 2006 Feb;14(2):249-52. doi: 10.1038/sj.ejhg.5201537. Eur J Hum Genet. 2006. PMID: 16333315

10

Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.

Bouhouche A, Benomar A, Bouslam N, Chkili T, Yahyaoui M. Bouhouche A, et al. J Med Genet. 2006 May;43(5):441-3. doi: 10.1136/jmg.2005.039230. Epub 2006 Jan 6. J Med Genet. 2006. PMID: 16399879 Free PMC article.

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