Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Rosette Jabbour"'
Autor:
Mahasen Reda, Rosette Jabbour, Asad Haydar, Fatima Jaafar, Nabil El Ayoubi, Omar Nawfal, Ahmad Beydoun
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundAnti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is one of the most prevalent etiologies of autoimmune encephalitis. Approximately 25% of anti-NMDAR encephalitis cases prove refractory to both first- and second-line treatments,
Externí odkaz:
https://doaj.org/article/a1d3cfcc13384c79b262b72fbc59db1d
Autor:
Rémi Bos, Khalil Rihan, Patrice Quintana, Lara El-Bazzal, Nathalie Bernard-Marissal, Nathalie Da Silva, Rosette Jabbour, André Mégarbané, Marc Bartoli, Frédéric Brocard, Valérie Delague
Publikováno v:
Neurobiology of Disease, Vol 164, Iss , Pp 105609- (2022)
We recently described new pathogenic variants in VRK1, in patients affected with distal Hereditary Motor Neuropathy associated with upper motor neurons signs. Specifically, we provided evidences that hiPSC-derived Motor Neurons (hiPSC-MN) from these
Externí odkaz:
https://doaj.org/article/e0889f703ae042e3a01c7a9e37be8b23
Publikováno v:
The Neurologist. 26:248-252
BACKGROUND Brucella are small, nonmotile, intracellular, and aerobic gram-negative bacteria. Of the 10 species that currently form the genus Brucella, 5 were shown to be pathogenic in humans. REVIEW SUMMARY The epidemiology, clinical manifestations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1196d73ea8cd6b385ee99e0b6661adb
https://doi.org/10.1097/nrl.0000000000000348
https://doi.org/10.1097/nrl.0000000000000348
Autor:
Andre Megarbane, Sami Bizzari, Asha Deepthi, Sandra Sabbagh, Hicham Mansour, Eliane Chouery, Ghassan Hmaimess, Rosette Jabbour, Cybel Mehawej, Saada Alame, Abeer Hani, Dana Hasbini, Ismat Ghanem, Salam Koussa, Mahmoud Taleb Al-Ali, Marc Obeid, Diana Bou Talea, Gerard Lefranc, Nicolas Lévy, France Leturcq, Stephany El Hayek, Valérie Delague, J. Andoni Urtizberea
Publikováno v:
Journal of Neuromuscular Diseases
Journal of Neuromuscular Diseases, 2022, 9 (1), pp.193-210. ⟨10.3233/JND-210652⟩
Journal of Neuromuscular Diseases, 2022, 9 (1), pp.193-210. ⟨10.3233/JND-210652⟩
Background: Clinical and molecular data on the occurrence and frequency of inherited neuromuscular disorders (NMD) in the Lebanese population is scarce. Objective: This study aims to provide a retrospective overview of hereditary NMDs based on our cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ef5fc9d8231e08324d8b33ef984239
https://pubmed.ncbi.nlm.nih.gov/34602496
https://pubmed.ncbi.nlm.nih.gov/34602496
Publikováno v:
Journal of Case Reports. :157-161
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bb3eb1474ebe21d949077fd3f0291c8
https://doi.org/10.17659/01.2019.0041
https://doi.org/10.17659/01.2019.0041
Autor:
Marc Bartoli, Quintana P, Nathalie Bernard-Marissal, Frédéric Brocard, Rémi Bos, Delague, Rosette Jabbour, André Mégarbané, Lara El-Bazzal, Rihan K
SummaryWe recently described new pathogenic variants in VRK1, in patients affected with distal Hereditary Motor Neuropathy associated with upper motor neurons signs. Specifically, we provided evidences that hiPSC-derived Motor Neurons (hiPSC-MN) from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18a962f244ebd511e8038ba49e3033cf
https://hal.archives-ouvertes.fr/hal-03411458
https://hal.archives-ouvertes.fr/hal-03411458
Autor:
Marc Bartoli, Salam Koussa, Nathalie Bernard-Marissal, Rosette Jabbour, Khalil Rihan, Christel Castro, André Mégarbané, Valérie Delague, Nicolas Lévy, Lara El-Bazzal, Alexandre Atkinson, Jean-Pierre Desvignes, Eliane Chouery-Khoury, Karine Bertaux
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz060⟩
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz060⟩
Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases, resembling Charcot–Marie–Tooth syndromes, but characterized by an exclusive involvement of the motor part of the peripheral nervous system. Here, we describe two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379ad8ce8f9b1eb0c81979c36fc1c62a
https://hal-amu.archives-ouvertes.fr/hal-02152040/document
https://hal-amu.archives-ouvertes.fr/hal-02152040/document
Publikováno v:
Journal of Neurosciences in Rural Practice
Journal of Neurosciences in Rural Practice, Vol 09, Iss 03, Pp 404-405 (2018)
Journal of Neurosciences in Rural Practice, Vol 09, Iss 03, Pp 404-405 (2018)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c41aafb8d2d4a386e52c99d16e2f240
http://europepmc.org/articles/PMC6050766
http://europepmc.org/articles/PMC6050766
Publikováno v:
Medicine. 90(5)
Toxocara myelitis is a rare disease. Few cases have been reported in the literature. Patients present with myelopathy, occasional eosinophilia in blood and cerebrospinal fluid (CSF), with abnormal signals on magnetic resonance imaging (MRI). In the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e07958fcbba88f9606d0199a79476f5
https://pubmed.ncbi.nlm.nih.gov/33257028
https://pubmed.ncbi.nlm.nih.gov/33257028
Autor:
Rosette Jabbour, Imad H. Elhajj
Publikováno v:
2008 5th International Multi-Conference on Systems, Signals and Devices.
Conventional priority-based queuing is regarded as one efficient way of imposing hierarchy on disparate traffic when it comes to delay, jitter, size etc... The basic method involves having multiple queues at the processing node, built atop a heap str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa5e022b049cffe74af95c3e340295ac
https://doi.org/10.1109/ssd.2008.4632789
https://doi.org/10.1109/ssd.2008.4632789