Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nesrine Baradai"'
Publikováno v:
Interdisciplinary Neurosurgery, Vol 25, Iss , Pp 101133- (2021)
Introduction: Tumor-like neurosarcoidosis is rare. It is found in 10% of cases of neurosarcoidosis (Cacoub et al., 2000) [1]. Observation: A 56-year-old woman presented with partial seizures, progressive right hemiparesis and aphasia. Brain magnetic
Externí odkaz:
https://doaj.org/article/bdace71c57c34d99a655f00bb2af6a26
Publikováno v:
Emerging Neurologist. 1:12-15
Introduction. Spinal cord involvement as a flare-up of Susac syndrome (SuS) is rarely reported in the literature. The pathogenesis of SuS includes multiple occlusions in micro vessels mediated by an autoimmune response to unknown antigens. This condi
Publikováno v:
Neurological Sciences. 43:565-571
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare affection of the peripheral nervous system. Its diagnostic criteria have evolved since 1975. The aim of our work is to study the epidemiological, clinical, and paraclinical as
Autor:
Nesrine Baradai, Saloua Mrabet, Nasri Amina, Alya Gharbi, Amira Souissi, Amina Gargouri-Berrechid, Mouna Djebara, Kacem Imen, Riadh Gouider
Publikováno v:
Revue Neurologique. 178:S30
Autor:
Sami Ben Rhouma, Marouane Boukhris, Mokhtar Bibi, Nesrine Baradai, Houcem Hedhli, Yassine Ouanes, Aziz Kacem, Kays Chaker, A. Sellami, Yassine Nouira, Kheireddine Mrad Deli
BackgroundThere are several factors explaining the difference in the spread of SARS-CoV-2 infection including the BCG vaccination. This fact is supported by the concept of beneficial non specific effect of this live vaccine associated to its interact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6875071770fcbabf2dd1b0ffa64d0b1e
Publikováno v:
Interdisciplinary Neurosurgery, Vol 25, Iss, Pp 101133-(2021)
Introduction Tumor-like neurosarcoidosis is rare. It is found in 10% of cases of neurosarcoidosis (Cacoub et al., 2000) [1] . Observation A 56-year-old woman presented with partial seizures, progressive right hemiparesis and aphasia. Brain magnetic r
Autor:
Damien Sternberg, Hedia Klaa, Hanene Benrhouma, Ilhem Ben Youssef-Turki, Nesrine Baradai, Ichraf Kraoua, Thouraya Ben Younes
Publikováno v:
Revue Neurologique. 177:S75
Introduction Le syndrome myasthenique congenital (SMC) est une pathologie rare de l’enfant d’origine genetique. Il est caracterise par un dysfonctionnement de la jonction neuromusculaire (JNM) et constitue une entite nosologique heterogene en ple