Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Amel Mrabet"'
Publikováno v:
Neurophysiologie clinique = Clinical neurophysiology. 49(3)
Publikováno v:
Neurophysiologie Clinique/Clinical Neurophysiology. 47:212-213
Objectif Determiner l’efficacite de la stimulation magnetique repetitive (r-TMS) dans le traitement des douleurs neuropathiques des patients tunisiens. Methodes Ont ete recrutes dans l’etude les patients adresses a l’unite de stimulation magnet
Autor:
Hela Mrabet Khiari, Amel Mrabet, Emna Khemiri, Nejib Hattab, Dominique Parain, Franois Proust
Publikováno v:
Seizure. 19:74-78
Objective To describe the first Tunisian epilepsy surgery program establishment and to emphasize on its originality that is an exchange and surgery decision taken by two Mediterranean neurophysiological teams, via the Internet. Methods Patients with
Publikováno v:
Revue Neurologique. 165:489-492
Resume Introduction Le syndrome de Parry-Romberg, affection rare d’etiologie inconnue, comporte une atrophie progressive d’une hemiface ou d’un hemicorps. Ses principales manifestations sont neurologiques, ophtalmologiques et cutanees. Les dysk
Publikováno v:
Neurological Sciences. 28:311-314
The objective was to investigate whether the described mutations of the SCN1A, SCN1B and GABRG2 genes are associated to generalised epilepsy with febrile seizure plus (GEFS+) in two Tunisian families. We performed a genetic study of two multigenerati
Autor:
Eric LeGuern, T. Taïeb, N. Birouk, Hamid Azzedine, Alexis Brice, Ahmed Bouhouche, T. Chkili, M. Di Duca, T. Hammadouche, Jocelyn Laporte, Alessandra Bolino, S. Benamou, Roberto Ravazzolo, R. Gouider, Amel Mrabet
Publikováno v:
The American Journal of Human Genetics. 72(5):1141-1153
Charcot-Marie-Tooth disease (CMT) with autosomal recessive (AR) inheritance is a heterogeneous group of inherited motor and sensory neuropathies. In some families from Japan and Brazil, a demyelinating CMT, mainly characterized by the presence of mye
Publikováno v:
Revue Neurologique. 167:861-863
Publikováno v:
Epilepsy & Behavior. 21:417-419
The medicolegal problems associated with posttraumatic epilepsy are frequently related to the assessment of the cause of traumatic brain injury and to the complexity of forensic examination. We carried out a study of 28 patients with posttraumatic ep
Publikováno v:
Revue Neurologique. 163:837-839
Resume Introduction Bien que les manifestations neuromusculaires soient frequentes au cours de l’evolution d’une hypothyroidie, la myotonie est exceptionnellement inaugurale de l’affection. Observations Deux patients, âges respectivement de 28
Autor:
Maria D. Lalioti, Hamish S. Scott, Amel Mrabet, Armand Bottani, T. Chkili, R. Gouider, Sadi Ibrahim, Alain Malafosse, Charlotte Dravet, Stylianos E. Antonarakis, Pierre Genton, Réda Ouazzani, D. Grid, Catherine Buresi
Publikováno v:
American Journal of Human Genetics, Vol. 62, No 4 (1998) pp. 842-847
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is a rare, autosomal recessive disorder characterized by onset at age 6-16 years, generalized seizures, incapacitating myoclonus, and variable progression to cerebellar ataxia. The