Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sabrine Rekik"'
Autor:
Ikhlass Belhassen, Salma Sakka, Sabrine Rekik, Daoued Sawssan, Mariem Dammak, Leturcq France, Chokri Mhiri
Publikováno v:
Revue Neurologique. 179:S110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffa8219730026c99554191dca6f864d3
https://doi.org/10.1016/j.neurol.2023.01.584
https://doi.org/10.1016/j.neurol.2023.01.584
Autor:
Sabrine Rekik, Myriam Ben Saad
Publikováno v:
28th Annual European Real Estate Society Conference.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b05a1977a79462672ba7d79630ca6a6
https://doi.org/10.15396/eres2022_44
https://doi.org/10.15396/eres2022_44
Autor:
Chokri Mhiri, Sabrine Rekik, Sawssan Ben Romdhan, Yasmine Baba Amer, François-Jérôme Authier, Nouha Farhat, Leila Lehkim, Salma Sakka
Publikováno v:
Journal of Molecular Neuroscience. 69:563-569
CAPN3 gene encodes for calpain-3; this protein is a calcium-dependent intracellular protease. Deficiency of this enzyme leads to weakness of the proximal limb muscles and pelvic and shoulder girdles, the so-called limb-girdle muscular dystrophy type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db4f272a24c85c74ba2e8333fde0949
https://doi.org/10.1007/s12031-019-01383-z
https://doi.org/10.1007/s12031-019-01383-z
Autor:
Leila Lehkim, François-Jérôme Authier, Sawsan Ben Romdhane, Nouha Farhat, Salma Sakka, Mariem Dammak, Khaireddine Ben Mahfoudh, Yasmine Baba Amer, Sabrine Rekik, Chokri Mhiri
Publikováno v:
Molecular biology reports. 47(8)
Dysferlinopathies belong to the heterogeneous group of autosomal recessive muscular disorders, caused by mutations in the dysferlin gene and characterized by a high degree of clinical variability even though within the same family. This study aims to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76e0e455e98d2a643b2a82e24009f535
https://pubmed.ncbi.nlm.nih.gov/32666437
https://pubmed.ncbi.nlm.nih.gov/32666437
Publikováno v:
International Journal of Intellectual Property Management
International Journal of Intellectual Property Management, Inderscience, 2019, 9 (2), pp.136-165. ⟨10.1504/IJIPM.2019.100213⟩
International Journal of Intellectual Property Management, Inderscience, 2019, 9 (2), pp.136-165. ⟨10.1504/IJIPM.2019.100213⟩
International audience; This paper analyses the optimal use of formal intellectual property rights (IPR) at the firm level. We examine the impact of combinations of IPR on the firm's productivity in order to study the complementarity or substitution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::158df7b4d6679b7dbcd280a1cd8f7155
https://hal.archives-ouvertes.fr/hal-03427803
https://hal.archives-ouvertes.fr/hal-03427803
Autor:
Olfa Hdiji, Hanen Haj Kacem, Chokri Mhiri, Sakka Salma, Sabrine Rekik, Baba Amer Yasmine, François-Jérôme Authier
Publikováno v:
Revue Neurologique. 175:S37-S38
Introduction L’etude des proteines est tres importante pour comprendre les correlations genotype-phenotype, ainsi pour ameliorer la strategie de diagnostic des maladies neuromusculaires specifiquement les myopathies autosomiques recessives (MAR). O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d4fac5a0d230225b485bdb052ac7d12
https://doi.org/10.1016/j.neurol.2019.01.123
https://doi.org/10.1016/j.neurol.2019.01.123
Publikováno v:
In Revue Neurologique April 2021 177 Supplement:S141-S142
Autor:
Nouha Farhat, Mariem Dammak, Kacem Hanen Hadj, Sakka Salma, Sabrine Rekik, Olfa Hdiji, Chokri Mhiri
Publikováno v:
Revue Neurologique. 174:S48-S49
Introduction Les sarcoglycanopathies sont des maladies musculaires genetiques a transmission autosomique recessive. Elles sont dues a une deficience d’une proteine du complexe sarcoglycane entrainant une instabilite de la membrane cellulaire. Objec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84d1c3f7a589d658b53c5e3227dfd7fa
https://doi.org/10.1016/j.neurol.2018.01.110
https://doi.org/10.1016/j.neurol.2018.01.110
Autor:
Nouha Bouzidi, Hanen Haj Kacem, Baba Amer Yasmine, Sabrine Rekik, François-Jérôme Authier, Sakka Salma, Chokri Mhiri
Publikováno v:
Revue Neurologique. 175:S40
Introduction La LGMD2B est une dystrophie musculaire causee par des mutations du gene dysferline. L’absence de la dysferline constitue un critere principal de diagnostic et indique une analyse mutationelle du gene. Objectifs Realiser une etude gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1190235d7e4b9d9f9c6c5672ef99202f
https://doi.org/10.1016/j.neurol.2019.01.129
https://doi.org/10.1016/j.neurol.2019.01.129