Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Istabrak Abdelkefi"'
Autor:
Youssef Sidhom, Mouna Ben Djebara, Yosr Hizem, Istabrak Abdelkefi, Imen Kacem, Amina Gargouri, Riadh Gouider
Publikováno v:
Behavioural Neurology, Vol 2014 (2014)
Background. The prevalence of psychiatric disturbance for patients with multiple sclerosis (MS) is higher than that observed in other chronic health conditions. We report three cases of MS and bipolar disorder and we discuss the possible etiological
Externí odkaz:
https://doaj.org/article/189c66cd99714f97bf3c709fcf16319b
Autor:
Atrous, Amal, Gharbi, Alya, Istabrak, Abdelkefi, Abida, Youssef, Souissi, Amira, Mrabet, Saloua, Gouider, Riadh
Publikováno v:
In Revue Neurologique April 2024 180 Supplement:S164-S165
Publikováno v:
Current Rheumatology Reviews. 16:343-345
Background: Stiff Person Syndrome (SPS) is a rare autoimmune neurological disorder which is often misdiagnosed. We report here a case of SPS with a long diagnosis delay. Case: A 36-year-old man presented with an 11-year history of progressive stiffne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c81d66cce12516b242ec3a64841569e
https://doi.org/10.2174/1573397115666191116101240
https://doi.org/10.2174/1573397115666191116101240
Autor:
Leila Ali, Kacem Imen, Saloua Mrabet, Istabrak Abdelkefi, Alya Gharbi, Amira Souissi, Amina Gargouri-Berrechid, Nasri Amina, Riadh Gouider
Publikováno v:
Revue Neurologique. 178:S11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e81dfc2f479161c8988f86798ff4f9bc
https://doi.org/10.1016/j.neurol.2022.02.144
https://doi.org/10.1016/j.neurol.2022.02.144
Autor:
Amina Nasri, Riadh Gouider, Yosr Hizem, Mouna Ben Djebrara, A. Gargouri-Berrechid, Youssef Sidhom, Imen Kacem, Istabrak Abdelkefi
Publikováno v:
Neurophysiologie Clinique/Clinical Neurophysiology. 46:119-124
Summary Objectives To describe the EEG characteristics of patients with Unverricht-Lundborg disease (ULD) and their changes during the long-term evolution of the disease. Methods A retrospective study including all patients with ULD confirmed by mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6f0a5168bd40a472b136fca0de983c1
https://doi.org/10.1016/j.neucli.2016.03.003
https://doi.org/10.1016/j.neucli.2016.03.003
Autor:
Saloua Mrabet, Istabrak Abdelkefi, Imen Kacem, A. Nasri, Riadh Gouider, M. Ben Djebara, A. Gargouri-Berrechid
Publikováno v:
Journal of the Neurological Sciences. 405:158-159
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf982be5056af4868a64fb3d0d72422f
https://doi.org/10.1016/j.jns.2019.10.1079
https://doi.org/10.1016/j.jns.2019.10.1079
Autor:
A. Gargouri-Berrechid, Saloua Mrabet, Fatma Laater, Istabrak Abdelkefi, Riadh Gouider, Imen Kacem, Mouna Ben Djebara
Publikováno v:
Revue Neurologique. 174:S24-S25
Introduction L’association des troubles psychiatriques a l’epilepsie generalisee idiopathique (EGI) rend son pronostic moins favorable. Objectifs Decrire la prevalence, le type des troubles psychiatriques et leurs relations aux differents sous-ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4eafdf1d196912961ec606a11cf227f9
https://doi.org/10.1016/j.neurol.2018.01.056
https://doi.org/10.1016/j.neurol.2018.01.056
Autor:
Saloua Mrabet, Istabrak Abdelkefi, Sirine Belghith, Amina Nasri, Imen Kacem, Amina Gargouri, Riadh Gouider
Publikováno v:
Revue Neurologique. 175:S19
Introduction La presence de troubles cognitifs est de plus en plus reconnue au cours de l’epilepsie genetique (EG). Leur presence s’associe a un mauvais pronostic de la maladie. Objectifs Etudier les facteurs determinants des troubles cognitifs a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f03d6056e4dac67bc468d9a492a9ef0
https://doi.org/10.1016/j.neurol.2019.01.079
https://doi.org/10.1016/j.neurol.2019.01.079
Autor:
Istabrak Abdelkefi, Amina Gargouri, Fatma Laatar, Mouna Ben Djebara, Kacem Imen, Riadh Gouider, Saloua Mrabet
Publikováno v:
Revue Neurologique. 173:S42-S43
Introduction L’epilepsie myoclonique juvenile (EMJ) est un syndrome epileptique âge dependant. Sur le plan cognitif, l’EMJ se caracterise par une atteinte predominante des fonctions frontales et executives. Objectifs Evaluer les troubles cogniti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09c42edaff0671b3e2ce81a4ecc6188b
https://doi.org/10.1016/j.neurol.2017.01.017
https://doi.org/10.1016/j.neurol.2017.01.017
Autor:
Amina Nasri, Mouna Ben Djebara, Kacem Imen, Fatma Laatar, Riadh Gouider, Istabrak Abdelkefi, Amina Gargouri
Publikováno v:
Revue Neurologique. 172:A21
Introduction L’EMJ est une entite electro-clinique frequente sa prevalence est de 10 % des epilepsies et 18 % des epilepsies generalisees idiopathiques. Quoique d’evolution generalement benigne, elle s’accompagne frequemment de troubles cogniti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63869a6c891a230599ba5c2db2b9f540
https://doi.org/10.1016/j.neurol.2016.01.042
https://doi.org/10.1016/j.neurol.2016.01.042