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[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. Among authors: rouissi a. 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.
Movement disorders in neuro-metabolic diseases.
Gouider-Khouja N, Kraoua I, Benrhouma H, Fraj N, Rouissi A. Gouider-Khouja N, et al. Among authors: rouissi a. 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.
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: rouissi a. 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.
[Epidemic of rubella encephalitis].
Ben Achour N, Benrhouma H, Rouissi A, Touaiti H, Kraoua I, Turki I, Gouider-Khouja N. Ben Achour N, et al. Among authors: rouissi a. Arch Pediatr. 2013 Aug;20(8):858-62. doi: 10.1016/j.arcped.2013.05.010. Epub 2013 Jul 5. Arch Pediatr. 2013. PMID: 23835099 French.
Lesch Nyhan syndrome: a novel complex mutation in a Tunisian child.
Rebai I, Kraoua I, Benrhouma H, Rouissi A, Turki I, Ceballos-Picot I, Gouider-Khouja N. Rebai I, et al. Among authors: rouissi a. Brain Dev. 2014 Nov;36(10):921-3. doi: 10.1016/j.braindev.2014.01.006. Epub 2014 Feb 3. Brain Dev. 2014. PMID: 24503445
31 results