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Saloua Fray

Showing results (1-10 of 13) with videos related to

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Neurocase|April 4, 2020
Refractory epilepsy in PSEN 1 mutation (I83T)Saloua Fray, Afef Rassas, Taieb Messaoud, et al.
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.
Epilepsy & Behavior : E&B|November 27, 2020
Utility of EEG on attention deficit-hyperactivity disorder (ADHD)Mariem Ben Mahmoud, Nadia Ben Ali, Saloua Fray, et al.
The Neurologist|November 4, 2021
COVID-19 Infection and Recurrent Stroke in Young Patients With Protein S Deficiency: A Case ReportLeila Ali, Hela Jamoussi, Nessrine Kouki, 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.
Epilepsy & Behavior : E&B|September 4, 2021
Knowledge and attitudes toward epilepsy among teachers in TunisiaEmna Sansa, Saloua Fray, Hela Jamoussi, 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)|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.
Multiple Sclerosis and Related Disorders|January 19, 2023
Cognitive impairment in multiple sclerosis: Utility of electroencephalographyHela Jamoussi, Nadia Ben Ali, Yasmine Missaoui, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Neurocase|April 4, 2020
Refractory epilepsy in PSEN 1 mutation (I83T)Saloua Fray, Afef Rassas, Taieb Messaoud, et al.
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.
Epilepsy & Behavior : E&B|November 27, 2020
Utility of EEG on attention deficit-hyperactivity disorder (ADHD)Mariem Ben Mahmoud, Nadia Ben Ali, Saloua Fray, et al.
The Neurologist|November 4, 2021
COVID-19 Infection and Recurrent Stroke in Young Patients With Protein S Deficiency: A Case ReportLeila Ali, Hela Jamoussi, Nessrine Kouki, 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.
Epilepsy & Behavior : E&B|September 4, 2021
Knowledge and attitudes toward epilepsy among teachers in TunisiaEmna Sansa, Saloua Fray, Hela Jamoussi, 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)|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.
Multiple Sclerosis and Related Disorders|January 19, 2023
Cognitive impairment in multiple sclerosis: Utility of electroencephalographyHela Jamoussi, Nadia Ben Ali, Yasmine Missaoui, et al.
Pageof 2