Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ahlem, Ben Hmid"'
Advancing understanding of the role of IL-22 in myelination: insights from the Cuprizone mouse model
Autor:
Imen Zamali, Ines Elbini, Raja Rekik, Nour-Elhouda Neili, Wafa Ben Hamouda, Ahlem Ben Hmid, Raoudha Doghri, Mélika Ben Ahmed
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Despite significant advancements in the field, the pathophysiology of multiple sclerosis (MS) remains partially understood, with limited therapeutic options available for this debilitating condition. The precise impact of Interleukin-22 (IL-22) in th
Externí odkaz:
https://doaj.org/article/77c666b7fad94b5f93b3812a7745eba3
Autor:
Mohamed Houssem Karamti, Hassane Zouhal, Mariem Bousselmi, Manel Darragi, Hamdi Khannous, Ahlem Ben Hmid, Imen Zamali, Mélika Ben Ahmed, Ismail Laher, Urs Granacher, Amira Zouita Ben Moussa
Publikováno v:
Sports, Vol 12, Iss 8, p 223 (2024)
This study proposes to monitor the physical, immune and cognitive responses and adaptations of elite rugby players throughout the season based on the loads performed. Anthropometric measurements, physical fitness tests (e.g., muscle strength and powe
Externí odkaz:
https://doaj.org/article/0d15ea396bd5464ebf11c47a72bdd3d9
Autor:
Ahmed Amine Ben Khlil, Imen Zamali, Dorra Belloumi, Mariem Gdoura, Ghassen Kharroubi, Soumaya Marzouki, Rym Dachraoui, Insaf Ben Yaiche, Soumaya Bchiri, Walid Hamdi, Manel Gharbi, Ahlem Ben Hmid, Samar Samoud, Yousr Galai, Lamia Torjmane, Saloua Ladeb, Jihene Bettaieb, Henda Triki, Nour Ben Abdeljelil, Tarek Ben Othman, Melika Ben Ahmed
Publikováno v:
Vaccines, Vol 12, Iss 2, p 174 (2024)
Background: Allogeneic hematopoietic stem cell transplantation (ASCT) induces acquired immunodeficiency, potentially altering vaccine response. Herein, we aimed to explore the clinical tolerance and the humoral and cellular immune responses following
Externí odkaz:
https://doaj.org/article/1dc0a25183314d92bf79c3ab6c9b8ae5
Autor:
Samar Samoud, Jihene Bettaieb, Mariem Gdoura, Ghassen Kharroubi, Feriel Ben Ghachem, Imen Zamali, Ahlem Ben Hmid, Sadok Salem, Ahmed Adel Gereisha, Mongi Dellagi, Nahed Hogga, Adel Gharbi, Amor Baccouche, Manel Gharbi, Chadha Khemissi, Ghada Akili, Wissem Slama, Nabila Chaieb, Yousr Galai, Hechmi Louzir, Henda Triki, Melika Ben Ahmed
Publikováno v:
Vaccines, Vol 11, Iss 8, p 1329 (2023)
(1) Background: This study aimed to compare the immunogenicity of the mix-and-match CoronaVac/BNT162b2 vaccination to the homologous CoronaVac/CoronaVac regimen. (2) Methods: We conducted a simple-blinded randomized superiority trial to measure SARS-
Externí odkaz:
https://doaj.org/article/8ed4be92ee5a4e68863538dec669f90b
Autor:
Melika Ben Ahmed, Hedia Bellali, Mariem Gdoura, Imen Zamali, Ouafa Kallala, Ahlem Ben Hmid, Walid Hamdi, Hela Ayari, Hajer Fares, Karim Mechri, Soumaya Marzouki, Henda Triki, Nissaf Ben Alaya, Mohamed Kouni Chahed, Anis Klouz, Sonia Sebai Ben Amor, Chiheb Ben Rayana, Myriam Razgallah Khrouf, Chokri Hamouda, Noomene Elkadri, Riadh Daghfous, Abdelhalim Trabelsi
Publikováno v:
Vaccines, Vol 10, Iss 8, p 1189 (2022)
Background: The mass vaccination campaign against SARS-CoV-2 was started in Tunisia on 13 March 2021 by using progressively seven different vaccines approved for emergency use. Herein, we aimed to evaluate the humoral and cellular immunity in subject
Externí odkaz:
https://doaj.org/article/42355f1350884b43bd3914750c185fcf
Autor:
Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, Imen Chelly, Hela Boudabbous, Hamza Dallali, Crystel Bonnet, Meriem Hechmi, Soumeya Bekri, Nadia Zitouna, Lotfi Zekri, Amel Tounsi, Rym Kefi, Jihene Marrakchi, Olfa Messaoud, Ichraf Kraoua, Sonia Maalej, Ilhem Turki Ben Youssef, Ahlem Ben Hmid, Fabrice Giraudet, Sami Bouchoucha, Neji Tebib, Ghazi Besbes, Christine Petit, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0258202 (2021)
Alpha-Mannosidosis (AM) is an ultra-rare storage disorder caused by a deficiency of lysosomal alpha-mannosidase encoded by the MAN2B1 gene. Clinical presentation of AM includes mental retardation, recurrent infections, hearing loss, dysmorphic featur
Externí odkaz:
https://doaj.org/article/569f864a04af411d83938661f5680131
Autor:
Samar Samoud, Jihene Bettaieb, Mariem Gdoura, Ghassen Kharroubi, Feriel Ben Ghachem, Imen Zamali, Ahlem Ben Hmid, Sadok Salem, Ahmed Adel Gereisha, Mongi Dellagi, Nahed Hogga, Adel Gharbi, Manel Gharbi, Chadha Khemissi, Ghada Akili, Wissem Slama, Nabila Chaieb, Yousr Galai, Hechmi Louzir, Henda Triki, Melika Ben Ahmed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a8a88b61d7746d63660111912022d6e
https://doi.org/10.2139/ssrn.4321506
https://doi.org/10.2139/ssrn.4321506
Autor:
Hend Chaker Masmoudi, Amal Rhili, Imen Zamali, Ahlem Ben Hmid, Melika Ben Ahmed, Myriam Razgallah Khrouf
Publikováno v:
Frontiers in Health Services. 2
COVID-19 pandemic underscored the need for a rapid tool supporting decision-makers in prioritizing patients in the immediate and overwhelming context of pandemics, where shortages in different healthcare resources are faced. We have proposed Multi-Cr
Autor:
Imen Zamali, Zeineb Meddeb, Dorra Bejar, Fatma Korbi, Ahlem Ben Hmid, Thara Laarbi, Mouldi Hidri, Kamel Bousslama, Melika Ben Ahmed
Publikováno v:
SSRN Electronic Journal.
Autor:
Soumeya Bekri, Olfa Messaoud, Cherine Charfeddine, Hela Boudabbous, Amel Tounsi, Meriem Hechmi, Lotfi Zekri, Rahma Mkaouar, Ghazi Besbes, Ahlem Ben Hmid, Christine Petit, R. M’rad, Neji Tebib, Sami Bouchoucha, Fabrice Giraudet, Rym Kefi, J. Marrakchi, Crystel Bonnet, Imen Chelly, Ichraf Kraoua, Hamza Dallali, Ilhem Turki Ben Youssef, Sonia Abdelhak, Nadia Zitouna, Zied Riahi, Sonia Maalej, Mediha Trabelsi
Publikováno v:
PLoS ONE
PLoS ONE, 2021, 16 (10), pp.e0258202. ⟨10.1371/journal.pone.0258202⟩
PLoS ONE, Vol 16, Iss 10, p e0258202 (2021)
PLoS ONE, 2021, 16 (10), pp.e0258202. ⟨10.1371/journal.pone.0258202⟩
PLoS ONE, Vol 16, Iss 10, p e0258202 (2021)
Alpha-Mannosidosis (AM) is an ultra-rare storage disorder caused by a deficiency of lysosomal alpha-mannosidase encoded by the MAN2B1 gene. Clinical presentation of AM includes mental retardation, recurrent infections, hearing loss, dysmorphic featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10eed9fa8dee83d1c67ef18ba710098
https://hal-pasteur.archives-ouvertes.fr/pasteur-04072687
https://hal-pasteur.archives-ouvertes.fr/pasteur-04072687