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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.
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.
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders.
Travaglini L, Brancati F, Silhavy J, Iannicelli M, Nickerson E, Elkhartoufi N, Scott E, Spencer E, Gabriel S, Thomas S, Ben-Zeev B, Bertini E, Boltshauser E, Chaouch M, Cilio MR, de Jong MM, Kayserili H, Ogur G, Poretti A, Signorini S, Uziel G, Zaki MS; International JSRD Study Group; Johnson C, Attié-Bitach T, Gleeson JG, Valente EM. Travaglini L, et al. Eur J Hum Genet. 2013 Oct;21(10):1074-8. doi: 10.1038/ejhg.2012.305. Epub 2013 Feb 6. Eur J Hum Genet. 2013. PMID: 23386033 Free PMC article.
[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: kraoua i. 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.
72 results