Birouk N - 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: birouk n. 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: birouk n. 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

[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: birouk n. Presse Med. 1995 Sep 30;24(28):1301-4. Presse Med. 1995. PMID: 7501622 French.

4

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: birouk n. Stroke. 1994 Apr;25(4):886-8. doi: 10.1161/01.str.25.4.886. Stroke. 1994. PMID: 8160236

5

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: birouk n. 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.

6

[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: birouk n. Rev Neurol (Paris). 2003 Mar;159(3):300-6. Rev Neurol (Paris). 2003. PMID: 12703046 French.

7

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

8

[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: birouk n. Rev Neurol (Paris). 2007 Apr;163(4):462-70. doi: 10.1016/s0035-3787(07)90422-1. Rev Neurol (Paris). 2007. PMID: 17452948 French.

9

[Dermatomyositis and Wilson disease].

el Alaoui-Faris M, Benabdeljalil M, Slassi I, Boutchiche M, Birouk N, Belaidi H, Saidi A, Chkili T. el Alaoui-Faris M, et al. Among authors: birouk n. Rev Neurol (Paris). 1994;150(5):391-2. Rev Neurol (Paris). 1994. PMID: 7878329 French.

10

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: birouk n. Rev Rhum Engl Ed. 1999 Jun;66(6):347-50. Rev Rhum Engl Ed. 1999. PMID: 10418065

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