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Multiple Sclerosis and Related Disorders|January 19, 2023
Cognitive impairment in multiple sclerosis: Utility of electroencephalographyHela Jamoussi, Nadia Ben Ali, Yasmine Missaoui, et al.Cytogenetic and Genome Research|March 1, 2018
TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?Marwa Daghsni, Saida Lahbib, Mohamed Fradj, et al.Molecular Biology Reports|April 5, 2024
Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlationsMaha Jamoussi, Faten Alaya, Hela Jamoussi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 29, 2011
High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian populationAfef Achouri Rassas, Hela Mrabet Khiari, Sondes Hadj Fredj, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|October 13, 2015
Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer diseaseAfef Achouri-Rassas, Nadia Ben Ali, Aroua Cherif, et al.Neurobiology of Aging|July 7, 2015
Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's diseaseAfef Achouri-Rassas, Nadia Ben Ali, Saloua Fray, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 16, 2018
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 patientsAmel Ben Chehida, Sana Ben Messaoud, Rim Ben Abdelaziz, et al.Neuropediatrics|October 12, 2018
Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young PatientsAmel Ben Chehida, Sana Ben Messaoud, Rim Ben Abdelaziz, et al.Pageof 2