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Journal of Genetics|October 13, 2022
Missing apolipoprotein E ε4 allele associated with nonamnestic Alzheimer's disease in a Tunisian populationSaloua Fray, Afef Achouri-Rassas, Samir Belal, et al.Neurological Research|March 29, 2022
Association between H2 haplotype of microtubule associated protein tau gene (deletion / insertion) with Alzheimer Disease in Tunisian patientsSaloua Fray, Afef Achouri Achouri-Rassas, Sondes Hadj Fredj, et al.Neurological Research|March 5, 2025
Genetic association study between rs2234253 (p.T96K) variant of TREM2 and Alzheimer's disease in a Tunisian populationAfef Achouri-Rassas, Saloua Fray, Zakaria Said, et al.Journal of Clinical Gastroenterology|July 20, 2016
Gastrointestinal Dysfunction and Neuropathologic Correlations in Parkinson DiseaseSaloua Mrabet, Nadia Ben Ali, Afef Achouri, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 4, 2011
Obsessive-compulsive disorder: a new risk factor for Alzheimer disease?Hela Mrabet Khiari, Afef Achouri, Nadia Ben Ali, et al.Neurochemical Research|December 12, 2013
Association between Alzheimer disease and the -491T allele of regulatory region polymorphism of Apolipoprotein E in a Tunisian populationAfef Achouri-Rassas, Sondes Hadj Fredj, Hela Mrabet Khiari, et al.Case Reports in Medicine|June 27, 2015
Parkinsonism and Sjögren's Syndrome: A Fortuitous Association or a Shared Immunopathogenesis?Mariem Kchaou, Nadia Ben Ali, Intissar Hmida, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 2, 2013
No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian populationAfef Achouri Rassas, Sondess Hadj Fredj, Hela Mrabet Khiari, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|December 24, 2015
Early psychiatrics symptoms in familial Alzheimer's disease with presenilin 1 mutation (I83T)Saloua Fray, Nadia Ben Ali, Afef Achouri Rassas, et al.Clinical Case Reports|December 30, 2022
A Tunisian patient with CLCN2-related leukoencephalopathyDina Ben Mohamed, Zacharia Saied, Samia Ben Sassi, et al.Pageof 2