Zobrazeno 1 - 10
of 134
pro vyhledávání: '"R. Mrissa"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Sarcoidosis is a multi-systemic granulomatosis of unknown cause, characterized by a clinical polymorphism. It results from interplay of environmental and genetic factors. The aim of our study was to describe sociodemographic and genetic characteristi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b28b30719e0cd9ac923b25a3b4b93f2
https://doi.org/10.21203/rs.3.rs-654818/v1
https://doi.org/10.21203/rs.3.rs-654818/v1
Autor:
Jamel Zaouali, Hajer Derbali, Ines Bedoui, Amina Nasri, R. Mrissa, Malek Mansour, Anis Riahi, M. Messelmani
Publikováno v:
La Revue de Médecine Interne. 37:840-843
Resume Introduction L’opsoclonus-myoclonus-ataxie (OMS) est un syndrome clinique qui peut etre d’origine paraneoplasique, infectieuse, post-infectieuse, post-vaccinale ou idiopathique. Observation Nous rapportons l’observation d’un homme de 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f669f36a66ba2a28b59d1354a4943c88
https://doi.org/10.1016/j.revmed.2016.02.012
https://doi.org/10.1016/j.revmed.2016.02.012
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
La Revue de medecine interne. 37(12)
Opsoclonus-myoclonus-ataxia (OMS) is a rare clinical syndrome, of paraneoplastic infectious, post-infectious, post-vaccinal or idiopathic origin.We report a 24-year-old young man who presented with gait disorder preceded by a febrile rash and retroau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b830e6299d8c5943061a257474480485
https://pubmed.ncbi.nlm.nih.gov/27036225
https://pubmed.ncbi.nlm.nih.gov/27036225
Autor:
F. M'sadek, B. Jemli, Bassem Louzir, S. Gargouri, J. Zaouali, S. Othmani, N. Ben Abdallah, N. Ben Abdelhafidh, R. Mrissa, R. Battikh, O. Azzouz, M. Yedeas
Publikováno v:
La Revue de Médecine Interne. 26:829-832
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e7d4ead0c1c380259c5b8b662dc7311
https://doi.org/10.1016/j.revmed.2005.04.025
https://doi.org/10.1016/j.revmed.2005.04.025
Autor:
N, Touati, M, Mansour, I, Bedoui, A, Kacem, H, Derbali, A, Riahi, M, Messelmani, J, Zaouali, N, Fekih-Mrissa, R, Mrissa
Publikováno v:
Revue neurologique. 171(11)
Sarcoidosis is a multisystemic granulomatous disease of unknown aetiology. Neurologic manifestations are found in 5 to 10% of cases.We conducted a retrospective study over 6-year period including 18 patients diagnosed with neurosarcoidosis in the Neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::185b5a2e6ca570352e6fe08e6505e70d
https://pubmed.ncbi.nlm.nih.gov/26648345
https://pubmed.ncbi.nlm.nih.gov/26648345
Autor:
N. Mrissa, Samir Belal, Rim Amouri, M. Ben Hamida, R. Mrissa, Fayçel Hentati, C. Ben Hamida, I. Turki
Publikováno v:
Neurology. 54:1408-1414
Objective: To report the clinical findings and the genetic linkage mapping of an autosomal recessive cerebellar ataxia associated to peripheral neuropathy, showing an early onset cerebellar ataxia with retained tendon reflexes (EOCA) phenotype. Backg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6449230d5d125847c275b3835cc69a6d
https://doi.org/10.1212/wnl.54.7.1408
https://doi.org/10.1212/wnl.54.7.1408
Autor:
A, Messadi, N, Fekih-Mrissa, J, Zaouali, S, Layouni, B, Nsiri, M, Yedeas, A, Raies, R, Mrissa, N, Gritli
Publikováno v:
Pathologie-biologie. 60(3)
Platelet-activating factor interacts with its specific receptor and mediates leucocytes transmigration into central nervous system and expression of HLA molecules on antigens-presenting cells. These features are the major characteristics of multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f84be5bc2c1cace5660c065736a351ee
https://pubmed.ncbi.nlm.nih.gov/21658861
https://pubmed.ncbi.nlm.nih.gov/21658861
Autor:
O, Ben Salem-Berrabah, N, Fekih-Mrissa, I, Louati, S, Layouni, J, Zaouali, B, N'siri, N, Gritli, R, Mrissa
Publikováno v:
Revue neurologique. 167(2)
The aim of the present study is to provide a clinical and etiological analysis of cerebral venous thrombosis (CVT) in the Tunisian population.This is a prospective monocentric study including 26 patients referred to the Neurology Department of the Mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e702b616d5a8e09e080e336219e717e4
https://pubmed.ncbi.nlm.nih.gov/20728912
https://pubmed.ncbi.nlm.nih.gov/20728912