Turki I - Search Results

1

Acute Movement Disorders in Childhood: A Cohort Study and Review of the Literature.

Benrhouma H, Nasri A, Klaa H, Ben Achour N, Rouissi A, Kraoua I, Turki I. Benrhouma H, et al. Among authors: turki i. Pediatr Emerg Care. 2021 Nov 1;37(11):e719-e725. doi: 10.1097/PEC.0000000000002017. Pediatr Emerg Care. 2021. PMID: 34469400 Review.

2

[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. Among authors: turki i. Rev Neurol (Paris). 2009 Dec;165(12):1111-6. doi: 10.1016/j.neurol.2008.08.014. Rev Neurol (Paris). 2009. PMID: 19108857 French.

3

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: turki 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.

4

[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. Among authors: turki i. 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.

5

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. Among authors: turki i. Neuropediatrics. 2013 Oct;44(5):281-5. doi: 10.1055/s-0033-1338133. Epub 2013 Apr 6. Neuropediatrics. 2013. PMID: 23564319 Review.

6

[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: turki 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.

7

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: turki i. 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

8

Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort.

Romani M, Kraoua I, Micalizzi A, Klaa H, Benrhouma H, Drissi C, Turki I, Castellana S, Mazza T, Valente EM, Gouider-Khouja N. Romani M, et al. Among authors: turki i. Eur J Neurol. 2015 Jan;22(1):178-86. doi: 10.1111/ene.12552. Epub 2014 Aug 27. Eur J Neurol. 2015. PMID: 25164370

9

Mixed movements disorders as an initial feature of pediatric lupus.

Mrabet S, Benrhouma H, Kraoua I, Naas A, Achour NB, Klaa H, Turki I. Mrabet S, et al. Among authors: turki i. Brain Dev. 2015 Oct;37(9):904-6. doi: 10.1016/j.braindev.2015.01.008. Epub 2015 Feb 28. Brain Dev. 2015. PMID: 25736974

10

[Encephalitis in a 12-year-old boy].

Benrhouma H, Nagi S, Kraoua I, Drissi C, Turki I, Hammouda MB. Benrhouma H, et al. Among authors: turki i. Arch Pediatr. 2015 Aug;22(8):875-6; 892-4. doi: 10.1016/j.arcped.2015.05.015. Epub 2015 Jul 2. Arch Pediatr. 2015. PMID: 26142769 French. No abstract available.

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