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Page 1
TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?
Daghsni M, Lahbib S, Fradj M, Sayeb M, Kelmemi W, Kraoua L, Kchaou M, Maazoul F, Echebbi S, Ben Ali N, Abdelhak S, M'rad R. Daghsni M, et al. Among authors: ben ali n. Cytogenet Genome Res. 2018;154(1):1-5. doi: 10.1159/000486945. Epub 2018 Feb 28. Cytogenet Genome Res. 2018. PMID: 29490292
Depression in multiple sclerosis.
Mrabet S, Ben Ali N, Kchaou M, Belal S. Mrabet S, et al. Among authors: ben ali n. Rev Neurol (Paris). 2014 Nov;170(11):700-2. doi: 10.1016/j.neurol.2014.07.017. Epub 2014 Oct 14. Rev Neurol (Paris). 2014. PMID: 25444450
[Predictors factors of refractory epilepsy in childhood].
Fray S, Ben Ali N, Kchaou M, Chebbi S, Belal S. Fray S, et al. Among authors: ben ali n. Rev Neurol (Paris). 2015 Oct;171(10):730-5. doi: 10.1016/j.neurol.2015.06.004. Epub 2015 Aug 28. Rev Neurol (Paris). 2015. PMID: 26318897 French.
A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Mansouri H, Boudabous H, Hakim K, Ben Ali N, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Azzouz H, Tebib N. Ben Chehida A, et al. Among authors: ben abdelaziz r, ben messaoud s, ben ali n, ben ameur z. J Pediatr Endocrinol Metab. 2018 Sep 25;31(9):979-986. doi: 10.1515/jpem-2018-0151. J Pediatr Endocrinol Metab. 2018. PMID: 30110253
Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Ben Ali N, Boudabous H, Ben Abdelaziz I, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Fradj M, Azzouz H, Tebib N. Ben Chehida A, et al. Among authors: ben abdelaziz r, ben messaoud s, ben ali n, ben ameur z, ben abdelaziz i. Neuropediatrics. 2019 Feb;50(1):22-30. doi: 10.1055/s-0038-1669786. Epub 2018 Oct 11. Neuropediatrics. 2019. PMID: 30308687
Relapse of acute lymphoblastic leukemia revealed by an optic neuropathy.
Jamoussi H, Kchaou M, Echebbi S, Fray S, Ben Ali N, Fredj M. Jamoussi H, et al. Among authors: ben ali n. Rev Neurol (Paris). 2020 Jan-Feb;176(1-2):131-136. doi: 10.1016/j.neurol.2018.12.012. Epub 2019 Sep 18. Rev Neurol (Paris). 2020. PMID: 31542177 No abstract available.
Adult-onset Rasmussen encephalitis and Parry Romberg syndrome overlap.
Jamoussi M, Jamoussi H, Fray S, Echebbi S, Ben Ali N, Fredj M. Jamoussi M, et al. Among authors: ben ali n. Neurol Sci. 2021 Nov;42(11):4815-4820. doi: 10.1007/s10072-021-05488-5. Epub 2021 Aug 6. Neurol Sci. 2021. PMID: 34357473 No abstract available.
44 results