Rouissi A - Search Results

1

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: rouissi a. Clin Genet. 2022 Aug;102(2):157-160. doi: 10.1111/cge.14145. Clin Genet. 2022. PMID: 35796208

2

[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.

3

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.

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

6

[Congenital stenosis of interventricular foramina revealed by recurrent intracranial hypertension].

Ben Achour N, Kraoua I, Rouissi A, Benrhouma H, Ben Youssef-Turki I, Jemel H, Gouider-Khouja N. Ben Achour N, et al. Among authors: rouissi a. Neurochirurgie. 2013 Apr;59(2):93-6. doi: 10.1016/j.neuchi.2013.02.004. Epub 2013 Apr 15. Neurochirurgie. 2013. PMID: 23598244 French.

7

[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.

8

Anti-NMDA receptor encephalitis mimicking a primary psychiatric disorder in a 13-year-old girl.

Ben Achour N, Ben Youssef-Turki I, Messelmani M, Kraoua I, Yaacoubi J, Klaa H, Rouissi A, Benrhouma H, Ben Ahmed M, Didelot A, Ducray F, Gouider-Khouja N. Ben Achour N, et al. Among authors: rouissi a. Turk Psikiyatri Derg. 2013 Summer;24(2):145-7. Turk Psikiyatri Derg. 2013. PMID: 23905172 English, Turkish. No abstract available.

9

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

10

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: rouissi a. 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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

31 results

Search Page