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Page 1
[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. Among authors: kraoua i. Tunis Med. 2008 Feb;86(2):202-4. Tunis Med. 2008. PMID: 18444552 French. No abstract available.
Movement disorders in neuro-metabolic diseases.
Gouider-Khouja N, Kraoua I, Benrhouma H, Fraj N, Rouissi A. Gouider-Khouja N, et al. Among authors: kraoua i. 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.
[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. Among authors: kraoua i. 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.
Seronegative myasthenia gravis with bladder dysfunction.
Marouani I, Kraoua I, Benrhouma H, Rebai I, Rouissi A, Koubaa S, Turki I, Dziri C, Gouider-Khouja N. Marouani I, et al. Among authors: kraoua i. Rev Neurol (Paris). 2012 Mar;168(3):299-300. doi: 10.1016/j.neurol.2011.07.017. Epub 2012 Feb 23. Rev Neurol (Paris). 2012. PMID: 22365108 No abstract available.
72 results