Yahyaoui M - Search Results

1

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. Among authors: yahyaoui m. J Neurol Sci. 1999 Jan 1;162(1):97-101. doi: 10.1016/s0022-510x(98)00284-6. J Neurol Sci. 1999. PMID: 10064178

2

Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.

Marzouki N, Benomar A, Yahyaoui M, Birouk N, Elouazzani M, Chkili T, Benlemlih M. Marzouki N, et al. Among authors: yahyaoui m. Eur J Med Genet. 2005 Jan-Mar;48(1):21-8. doi: 10.1016/j.ejmg.2005.01.014. Epub 2005 Feb 19. Eur J Med Genet. 2005. PMID: 15953402

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: yahyaoui m. Can J Neurol Sci. 2007 Nov;34(4):421-6. doi: 10.1017/s0317167100007290. Can J Neurol Sci. 2007. PMID: 18062449

4

[Fahr syndrome and dysparathyroidism. 3 cases].

el Maghraoui A, Birouk N, Zaim A, Slassi I, Yahyaoui M, Chkili T. el Maghraoui A, et al. Among authors: yahyaoui m. Presse Med. 1995 Sep 30;24(28):1301-4. Presse Med. 1995. PMID: 7501622 French.

5

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. Among authors: yahyaoui m. Stroke. 1994 Apr;25(4):886-8. doi: 10.1161/01.str.25.4.886. Stroke. 1994. PMID: 8160236

6

Polyradiculoneuropathy revealing a solitary plasmacytoma of the ilium. A new case-report.

Niamane R, Benomar A, Messouak W, Benabdejlil M, Benabdellah C, Yahyaoui M, Hajjaj-Hassouni N, Chkili T. Niamane R, et al. Among authors: yahyaoui m. Rev Rhum Engl Ed. 1999 Apr;66(4):229-31. Rev Rhum Engl Ed. 1999. PMID: 10339780

7

Vitamin D deficiency and its role in neurological conditions: A review.

Mpandzou G, Aït Ben Haddou E, Regragui W, Benomar A, Yahyaoui M. Mpandzou G, et al. Among authors: yahyaoui m. Rev Neurol (Paris). 2016 Feb;172(2):109-22. doi: 10.1016/j.neurol.2015.11.005. Epub 2016 Feb 8. Rev Neurol (Paris). 2016. PMID: 26867662 Review.

8

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: yahyaoui m. Arch Neurol. 2003 Apr;60(4):598-604. doi: 10.1001/archneur.60.4.598. Arch Neurol. 2003. PMID: 12707075

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

10

A novel locus for autosomal recessive spastic ataxia on chromosome 17p.

Bouslam N, Bouhouche A, Benomar A, Hanein S, Klebe S, Azzedine H, Di Giandomenico S, Boland-Augé A, Santorelli FM, Durr A, Brice A, Yahyaoui M, Stevanin G. Bouslam N, et al. Among authors: yahyaoui m. Hum Genet. 2007 May;121(3-4):413-20. doi: 10.1007/s00439-007-0328-0. Epub 2007 Feb 2. Hum Genet. 2007. PMID: 17273843

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