Benomar A - Search Results

1

Clinical and genetic data of Huntington disease in Moroccan patients.

Bouhouche A, Regragui W, Lamghari H, Khaldi K, Birouk N, Lytim S, Bellamine S, Kriouile Y, Bouslam N, Haddou el HA, Faris MA, Benomar A, Yahyaoui M. Bouhouche A, et al. Among authors: benomar a. Afr Health Sci. 2015 Dec;15(4):1232-8. doi: 10.4314/ahs.v15i4.23. Afr Health Sci. 2015. PMID: 26958025 Free PMC article.

2

Middle cerebral artery occlusion due to hydatid cysts of myocardial and intraventricular cavity cardiac origin. Two cases.

Benomar A, Yahyaoui M, Birouk N, Vidailhet M, Chkili T. Benomar A, et al. Stroke. 1994 Apr;25(4):886-8. doi: 10.1161/01.str.25.4.886. Stroke. 1994. PMID: 8160236

3

Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).

David G, Dürr A, Stevanin G, Cancel G, Abbas N, Benomar A, Belal S, Lebre AS, Abada-Bendib M, Grid D, Holmberg M, Yahyaoui M, Hentati F, Chkili T, Agid Y, Brice A. David G, et al. Among authors: benomar a. Hum Mol Genet. 1998 Feb;7(2):165-70. doi: 10.1093/hmg/7.2.165. Hum Mol Genet. 1998. PMID: 9425222

4

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

Meggouh F, Benomar A, Rouger H, Tardieu S, Birouk N, Tassin J, Barhoumi C, Yahyaoui M, Chkili T, Brice A, LeGuern E. Meggouh F, et al. Among authors: benomar a. J Med Genet. 1998 Mar;35(3):251-2. doi: 10.1136/jmg.35.3.251. J Med Genet. 1998. PMID: 9541114 Free PMC article.

5

Vitamin E deficiency ataxia associated with adenoma.

Benomar A, Yahyaoui M, Marzouki N, Birouk N, Bouslam N, Belaidi H, Amarti A, Ouazzani R, Chkili T. Benomar A, et al. J Neurol Sci. 1999 Jan 1;162(1):97-101. doi: 10.1016/s0022-510x(98)00284-6. J Neurol Sci. 1999. PMID: 10064178

6

Rigid spine syndrome. Two case-reports.

Niamane R, Birouk N, Benomar A, Benabdejlil M, Amarti A, Yahyaoui M, Chkili T, Hajjaj-Hassouni N. Niamane R, et al. Among authors: benomar a. Rev Rhum Engl Ed. 1999 Jun;66(6):347-50. Rev Rhum Engl Ed. 1999. PMID: 10418065

7

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. Among authors: benomar a. Am J Hum Genet. 1999 Sep;65(3):722-7. doi: 10.1086/302542. Am J Hum Genet. 1999. PMID: 10441578 Free PMC article.

8

[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: benomar a. Rev Neurol (Paris). 2002 Jan;158(1):74-6. Rev Neurol (Paris). 2002. PMID: 11938326 French.

9

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. 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

10

[Wilson's disease. Clinical presentation, treatment and evolution in 21 cases].

Bono W, Moutie O, Benomar A, Aïdi S, el Alaoui-Faris M, Yahyaoui M, Chkili T. Bono W, et al. Among authors: benomar a. Rev Med Interne. 2002 May;23(5):419-31. doi: 10.1016/s0248-8663(02)00589-1. Rev Med Interne. 2002. PMID: 12064213 French.

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