Gouider-Khouja N - Search Results

1

[Neurological complications of acute intermittent porphyria precipitated by porphyrinogenic drugs and efficiency of heme-arginate treatment].

Akopova-Larbi R, Ben Youssef TI, Gargouri A, Kraoua I, Gouider R, Gouider-Khouja N. Akopova-Larbi R, et al. Tunis Med. 2009 Sep;87(9):621-6. Tunis Med. 2009. PMID: 20180386 Free article. French.

2

[Hemifacial spasm and its treatment with botulinum toxin].

Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. Gouider-Khouja N, et al. Tunis Med. 1999 Jan;77(1):41-4. Tunis Med. 1999. PMID: 10333697 Clinical Trial. French. No abstract available.

3

[Treatment of cervical dystonia with botulinum toxin].

Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. Gouider-Khouja N, et al. Tunis Med. 1999 Feb;77(2):101-4. Tunis Med. 1999. PMID: 10333707 French. No abstract available.

4

[Slow channel syndrome: clinical and neurophysiological aspects].

Ben Youssef Turki I, Kraoua I, Gargouri A, Akopova-Larbi R, Gouider R, Gouider-Khouja N. Ben Youssef Turki I, et al. Tunis Med. 2008 Feb;86(2):202-4. Tunis Med. 2008. PMID: 18444552 French. No abstract available.

5

[Cerebromediastinal tuberculosis in a child with a probable Say-Barber-Miller syndrome: a causative link?].

Kechaou I, Rouissi A, Kraoua I, Regayeg A, Turki I, Ben Hamouda M, Gouider-Khouja N. Kechaou I, et al. Rev Neurol (Paris). 2009 Dec;165(12):1111-6. doi: 10.1016/j.neurol.2008.08.014. Rev Neurol (Paris). 2009. PMID: 19108857 French.

6

[An overview of neurometabolic diseases in Tunisia. a 3-year prospective study].

Kraoua I, Benrhouma H, Rouissi A, Youssef-Turki IB, Zouari B, Kaabachi N, Gouider-Khouja N. Kraoua I, et al. Rev Neurol (Paris). 2009 Jun-Jul;165(6-7):568-74. doi: 10.1016/j.neurol.2008.10.027. Epub 2009 Jan 24. Rev Neurol (Paris). 2009. PMID: 19168196 French.

7

Movement disorders in neuro-metabolic diseases.

Gouider-Khouja N, Kraoua I, Benrhouma H, Fraj N, Rouissi A. Gouider-Khouja N, et al. Eur J Paediatr Neurol. 2010 Jul;14(4):304-7. doi: 10.1016/j.ejpn.2009.11.005. Epub 2009 Dec 16. Eur J Paediatr Neurol. 2010. PMID: 20015670 Review.

8

[A genetically confirmed CMT1A mimicking relapsing CIDP].

Ben Youssef-Turki I, Kraoua I, Gargouri A, Bouche P, Leguern E, Gouider-Khouja N. Ben Youssef-Turki I, et al. Rev Neurol (Paris). 2011 Dec;167(12):958-9. doi: 10.1016/j.neurol.2011.05.004. Epub 2011 Nov 5. Rev Neurol (Paris). 2011. PMID: 22056228 French. No abstract available.

9

[Clinical and therapeutic aspects in Tunisian patients with dystonia: a 5-year prospective study].

Benrhouma H, Kraoua I, Klaa H, Rouissi A, Turki I, Gouider-Khouja N. Benrhouma H, et al. Rev Neurol (Paris). 2013 Jan;169(1):47-52. doi: 10.1016/j.neurol.2012.01.586. Epub 2012 May 23. Rev Neurol (Paris). 2013. PMID: 22633313 French.

10

3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature.

Kraoua I, Wiame E, Kraoua L, Nasrallah F, Benrhouma H, Rouissi A, Turki I, Chaabouni H, Briand G, Kaabachi N, Van Schaftingen E, Gouider-Khouja N. Kraoua I, et al. Neuropediatrics. 2013 Oct;44(5):281-5. doi: 10.1055/s-0033-1338133. Epub 2013 Apr 6. Neuropediatrics. 2013. PMID: 23564319 Review.

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