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Neurocase
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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 population
Saloua 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 patients
Saloua 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 Report
Leila 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 population
Afef Achouri-Rassas, Saloua Fray, Zakaria Said, et al.
Epilepsy & Behavior : E&B
|
September 4, 2021
Knowledge and attitudes toward epilepsy among teachers in Tunisia
Emna 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 electroencephalography
Hela Jamoussi, Nadia Ben Ali, Yasmine Missaoui, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 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 population
Saloua 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 patients
Saloua 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 Report
Leila 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 population
Afef Achouri-Rassas, Saloua Fray, Zakaria Said, et al.
Epilepsy & Behavior : E&B
|
September 4, 2021
Knowledge and attitudes toward epilepsy among teachers in Tunisia
Emna 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 electroencephalography
Hela Jamoussi, Nadia Ben Ali, Yasmine Missaoui, et al.
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of 2