Mrabet S - Search Results

1

Determinants of cognitive impairment in multiple system atrophy: Clinical and genetic study.

Nasri A, Gharbi A, Sghaier I, Mrabet S, Souissi A, Gargouri A, Djebara MB, Kacem I, Gouider R. Nasri A, et al. Among authors: mrabet s. PLoS One. 2022 Dec 12;17(12):e0277798. doi: 10.1371/journal.pone.0277798. eCollection 2022. PLoS One. 2022. PMID: 36508411 Free PMC article.

2

[Neuropsychiatric manifestations ushering pernicious anemia].

Mrabet S, Ellouze F, Ellini S, Mrad MF. Mrabet S, et al. Encephale. 2015 Dec;41(6):550-5. doi: 10.1016/j.encep.2015.07.004. Epub 2015 Sep 4. Encephale. 2015. PMID: 26345354 French.

3

[Iconographic rubric. Pseudomyxoma peritonei complicating cancer of the rectum].

Khaldi F, Ben Chehida F, Mrabet S, Ben Becher S, Boudhina T, Bennaceur B. Khaldi F, et al. Among authors: mrabet s. Arch Fr Pediatr. 1993 Jan;50(1):55-6. Arch Fr Pediatr. 1993. PMID: 8507142 French. No abstract available.

4

[Scurvy in children].

Fejji S, Mongalgi MA, Boukthir S, M'Rabet S, Debbabi A. Fejji S, et al. Pediatrie. 1993;48(12):898-901. Pediatrie. 1993. PMID: 8047402 French.

5

Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes.

Landoulsi Z, Laatar F, Noé E, Mrabet S, Ben Djebara M, Achaz G, Nava C, Baulac S, Kacem I, Gargouri-Berrechid A, Gouider R, Leguern E. Landoulsi Z, et al. Among authors: mrabet s. Neurogenetics. 2018 Aug;19(3):165-178. doi: 10.1007/s10048-018-0550-z. Epub 2018 Jun 12. Neurogenetics. 2018. PMID: 29948376

6

Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg disease.

Berrechid AG, Bendjebara M, Bouteiller D, Nasri A, Peuvion JN, Marie Y, Baulac S, Mrabet S, Ribierre T, Cazeneuve C, Imenkacem, Leguern E, Gouider R. Berrechid AG, et al. Among authors: mrabet s. Epileptic Disord. 2019 Aug 1;21(4):359-365. doi: 10.1684/epd.2019.1078. Epileptic Disord. 2019. PMID: 31368437

7

Multiple sclerosis 2017 McDonald criteria are also relevant for Tunisians.

Souissi A, Mrabet S, Nasri A, Larnaout F, Bendjebara M, Gargouri A, Kacem I, Gouider R. Souissi A, et al. Among authors: mrabet s. Mult Scler Relat Disord. 2020 Aug;43:102161. doi: 10.1016/j.msard.2020.102161. Epub 2020 May 22. Mult Scler Relat Disord. 2020. PMID: 32534445

8

Atypical parkinsonian syndromes in a North African tertiary referral center.

Nasri A, Ben Djebara M, Sghaier I, Mrabet S, Zidi S, Gargouri A, Kacem I, Gouider R. Nasri A, et al. Among authors: mrabet s. Brain Behav. 2021 Jan;11(1):e01924. doi: 10.1002/brb3.1924. Epub 2020 Nov 11. Brain Behav. 2021. PMID: 33179436 Free PMC article.

9

Characteristics, onset, and evolution of neurological symptoms in patients with COVID-19.

Kacem I, Gharbi A, Harizi C, Souissi E, Safer M, Nasri A, Letaief H, Akkari M, Hechaichi A, Mrabet S, Dhaouadi S, Ben Djebara M, Derouiche S, Gargouri A, Chahed M, Ben Alaya N, Gouider R. Kacem I, et al. Among authors: mrabet s. Neurol Sci. 2021 Jan;42(1):39-46. doi: 10.1007/s10072-020-04866-9. Epub 2020 Nov 17. Neurol Sci. 2021. PMID: 33201360 Free PMC article.

10

Sensitivity of Awaji Criteria and Revised El Escorial Criteria in the Diagnosis of Amyotrophic Lateral Sclerosis (ALS) at First Visit in a Tunisian Cohort.

Ido BJF, Kacem I, Ouedraogo M, Nasri A, Mrabet S, Gargouri A, Ben Djebara M, Kabore BJ, Gouider R. Ido BJF, et al. Among authors: mrabet s. Neurol Res Int. 2021 Jan 22;2021:8841281. doi: 10.1155/2021/8841281. eCollection 2021. Neurol Res Int. 2021. PMID: 33552600 Free PMC article.

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