Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rim, Sebai"'
Autor:
Rim Sebai, S. Nagi, Cyrine Drissi, M. Araar, Nadia Hammami, Y. Maatallah, M. Ben Hamouda, L. Belghith, Fayçal Hentati
Publikováno v:
Journal of Neuroradiology. 34:133-136
We report the neuroimaging findings of a case of reversible metronidazole-induced encephalopathy. Magnetic resonance imaging (MRI) demonstrated lesions in highly suggestive locations. Follow-up imaging performed 1 month after cessation of metronidazo
Autor:
Cyrine Drissi, Rim Sebai, Zeineb Ouerghi, Mohamed Ben Hammouda, Sonia Nagi, Hammami Nadia, Anis Riahi
Publikováno v:
Revue Neurologique. 171:A45-A46
Introduction L’hemorragie cerebelleuse a distance du site operatoire (HCD) est une complication rare et imprevisible en neurochirurgie, dont les mecanismes physiopathologiques sont encore discutes. Objectifs Le but de notre travail est d’analyser
Autor:
Kamel Walha, Rim Sebai, Sonia Nagi, Aymen Arous, Cyrine Drissi, Mohamed Ben Hammouda, Anis Riahi
Publikováno v:
Revue Neurologique. 171:A19
Introduction La paralysie brutale du nerf oculomoteur commun est souvent causee par une compression anevrysmale. Cependant, des rares cas de conflit vasculo-nerveux par l’artere cerebrale posterieure ont ete rapportes. Observation Nous rapportons l
Autor:
Houda, Megdiche Bazarbacha, Mohamed, Bouchriha, Rim, Sebai, Lotfi, Belghith, Slaheddine, Touibi
Publikováno v:
La Tunisie medicale. 84(8)
Hemangiocytoma are rare malignant vascular tumor. Vertebral location is uncommun. They occur preferentially at the lumbo-sacrul spine with paravertebral extension. The features include spinal pains, para vertebral tumefaction and paresthesia. The CT
Autor:
Houda, Megdiche Bazarbacha, Sonia, Nagi, Wièm, Douira Khomsi, Rim, Sebai, Lotfi, Belghith, Slaheddine, Touibi
Publikováno v:
La Tunisie medicale. 82(12)
Recently, there have been several case reports of cavernous angiomas appearing after radiation to the brain, typically in children. The time interval between irradiation and the detection of the cavernous angioma varied from three to nine years and t
Publikováno v:
Neuroradiology. 42(5)
We report radiological features of a biopsy-proven early infantile form of Nasu-Hakola disease in two Tunisian sisters with new bony and cerebral findings.