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Autor:
Amina Nasri, Alya Gharbi, Ikram Sghaier, Saloua Mrabet, Amira Souissi, Amina Gargouri, Mouna Ben Djebara, Imen Kacem, Riadh Gouider
Publikováno v:
PLoS ONE, Vol 17, Iss 12, p e0277798 (2022)
IntroductionClassically, cognitive impairment (CI) was not considered as a paramount feature of multiple system atrophy(MSA) in both parkinsonian(MSA-P) and cerebellar(MSA-C) motor-subtypes. Yet, growing evidence indicates currently the commonness of
Externí odkaz:
https://doaj.org/article/cd12d611c0874b72962c20040f869983
Autor:
Amina Nasri, Mouna Ben Djebara, Ikram Sghaier, Saloua Mrabet, Sabrina Zidi, Amina Gargouri, Imen Kacem, Riadh Gouider
Publikováno v:
Brain and Behavior, Vol 11, Iss 1, Pp n/a-n/a (2021)
Abstract Introduction Data on epidemiology of atypical parkinsonian syndromes (APS) in North African countries are limited. Our objective was to study the epidemiological features of APS in a Tunisian population. Methods We conducted a 17‐year retr
Externí odkaz:
https://doaj.org/article/bcc78200ee4e48c5bda4a18e41fa3bc7
Autor:
Bademain Jean Fabrice Ido, Imen Kacem, Mahamadi Ouedraogo, Amina Nasri, Saloua Mrabet, Amina Gargouri, Mouna Ben Djebara, Bawindsongré Jean Kabore, Riadh Gouider
Publikováno v:
Neurology Research International, Vol 2021 (2021)
Background. Amyotrophic lateral sclerosis (ALS) is a fatal disease whose diagnosis and early management can improve survival. The most used diagnostic criteria are the revised El Escorial criteria (rEEC) and Awaji criteria (AC). The comparison of the
Externí odkaz:
https://doaj.org/article/0da00c0dac7549628de27ed04a59eada
Autor:
Zied Landoulsi, Sawssan Benromdhan, Mouna Ben Djebara, Mariem Damak, Hamza Dallali, Rym Kefi, Sonia Abdelhak, Amina Gargouri-Berrechid, Chokri Mhiri, Riadh Gouider
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background In North African populations, G2019S mutation in LRRK2 gene, encoding for the leucine-rich repeat kinase 2, is the most prevalent mutation linked to familial and sporadic Parkinson’s disease (PD). Early detection of G2019S by fa
Externí odkaz:
https://doaj.org/article/7cee80f17c07414099568c49ea6f490c
Publikováno v:
Clinical Neuropharmacology. 45:89-94
The prevalence of akathisia is variably reported in the literature and its psychiatric impact is little studied. The aim of this study was to establish the prevalence, the associated factors, and the psychiatric impact of akathisia among patients und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::601e376fb8d24e374cbc22e406f8fbaa
https://doi.org/10.1097/wnf.0000000000000506
https://doi.org/10.1097/wnf.0000000000000506
Autor:
Arwa Rekik, Saloua Mrabet, Imen Kacem, Amina Nasri, Mouna Ben Djebara, Amina Gargouri, Riadh Gouider
Publikováno v:
Neuroophthalmology
Few studies have reported abnormal ocular movements in cases of amyotrophic lateral sclerosis (ALS) and their link with other disease features. Our study aimed to describe and analyse eye movement abnormalities in ALS patients. Specifically, we set o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dfb54cfcff1796275d37b8491aec957
https://doi.org/10.1080/01658107.2022.2038638
https://doi.org/10.1080/01658107.2022.2038638
Autor:
Amina Nasri, Amina Gargouri, Eric LeGuern, Mouna Ben Djebara, Riadh Gouider, Imen Kacem, Sabrina Zidi, Saloua Mrabet
Publikováno v:
Epileptic Disorders. 24:163-170
Unverricht-Lundborg disease (ULD), also called progressive myoclonic epilepsy type 1, is usually characterized by the presence of ataxia associated with myoclonus and epileptic seizures without progressive cognitive deficit, presenting during late ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2425d4355604236b91781968137c993b
https://doi.org/10.1684/epd.2021.1372
https://doi.org/10.1684/epd.2021.1372
Autor:
Imen Kacem, Ikram Sghaier, Nicola Ticozzi, Saloua Mrabet, Silvia Paverelli, Amina Nasri, Antonia Ratti, Mouna Ben Djebara, Amina Gargouri-Berrachid, Vincenzo Silani, Riadh Gouider
Publikováno v:
Amyotrophic lateral sclerosisfrontotemporal degeneration. 23(7-8)
We describe a Tunisian family carrier of the same rare mutation iniTARDBP/ibut developing different neurodegenerative disease with heterogenous features. We explored the possible genetic modifiers leading to the observed intrafamilial phenotypic vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::049e30e816a5b428686965d3ba0a40d0
https://pubmed.ncbi.nlm.nih.gov/35793404
https://pubmed.ncbi.nlm.nih.gov/35793404
Autor:
Manel Akkari, Mouna Safer, Emira Souissi, Aicha Hechaichi, Imen Kacem, Mouna Ben Djebara, Nissaf Ben Alaya, Riadh Gouider, M.K. Chahed, Chahida Harizi, Hajer Letaief, Saloua Mrabet, Alya Gharbi, Sonia Dhaouadi, Sondes Derouiche, Amina Gargouri, Amina Nasri
Publikováno v:
Neurological Sciences
Background A wide range of neurological manifestations has been described in COVID-19. Methods In this nationwide retrospective observational study, patients in Tunisia diagnosed with COVID-19 between the 2nd of March and the 16th of May 2020 were co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5d06bc6b4343613b69659534d127e81
https://doi.org/10.1007/s10072-020-04866-9
https://doi.org/10.1007/s10072-020-04866-9