Kraoua I - Search Results

1

Parkinsonism in Gaucher's disease type 1: ten new cases and a review of the literature.

Kraoua I, Stirnemann J, Ribeiro MJ, Rouaud T, Verin M, Annic A, Rose C, Defebvre L, Réménieras L, Schüpbach M, Belmatoug N, Vidailhet M, Sedel F. Kraoua I, et al. Mov Disord. 2009 Jul 30;24(10):1524-30. doi: 10.1002/mds.22593. Mov Disord. 2009. PMID: 19513999 Review.

2

A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients.

Kraoua I, Sedel F, Caillaud C, Froissart R, Stirnemann J, Chaurand G, Flodrops H, Tari S, Gourfinkel-An I, Mathieu S, Belmatoug N, Billette de Villemeur T, Mignot C. Kraoua I, et al. Brain Dev. 2011 Feb;33(2):131-9. doi: 10.1016/j.braindev.2010.02.005. Epub 2010 Mar 21. Brain Dev. 2011. PMID: 20307947

3

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: kraoua 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

4

Childhood opsoclonus-myoclonus syndrome: A case series from Tunisia.

Ben Achour N, Mrabet S, Rebai I, Abid I, Benrhouma H, Klaa H, Rouissi A, Kraoua I, Ben Youssef Turki I. Ben Achour N, et al. Among authors: kraoua i. Brain Dev. 2017 Oct;39(9):751-755. doi: 10.1016/j.braindev.2017.05.001. Epub 2017 May 23. Brain Dev. 2017. PMID: 28549713

5

Neuronal ceroïd-lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series.

Ben Younes T, Kraoua I, Snanoudj S, Klaa H, Benrhouma H, Rouissi A, Caillaud C, Chaabouni M, Miladi N, Bekri S, Ben Youssef-Turki I. Ben Younes T, et al. Among authors: kraoua i. Clin Genet. 2022 Aug;102(2):157-160. doi: 10.1111/cge.14145. Clin Genet. 2022. PMID: 35796208

6

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.

7

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood.

Rebai I, Ben Rhouma H, Kraoua I, Klaa H, Rouissi A, Ben Youssef-Turki I, Gouider-Khouja N. Rebai I, et al. Among authors: kraoua i. Brain Dev. 2015 Jan;37(1):153-7. doi: 10.1016/j.braindev.2014.03.009. Epub 2014 Apr 16. Brain Dev. 2015. PMID: 24745788 Review.

8

[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.

9

[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: kraoua 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.

10

[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.

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