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BMC Neurology|October 7, 2020
Prior treatment status: impact on the efficacy and safety of teriflunomide in multiple sclerosisGiancarlo Comi, Mark S Freedman, José E Meca-Lallana, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|July 2, 2013
Agonists of MAS oncogene and angiotensin II type 2 receptors attenuate cardiopulmonary disease in rats with neonatal hyperoxia-induced lung injuryGerry T M Wagenaar, El Houari Laghmani, Melissa Fidder, et al.
Scientific Reports|August 24, 2025
Synthesis, crystal structure, DFT calculations, in-vitro and in-silico studies of novel chromone-isoxazoline conjugates as antibacterial and anti-inflammatory agentsRachid Bouzammit, Naoufal El Hachlafi, Mohamed El Fadili, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|September 17, 2023
Clinical features and outcomes of patients with pancreatic cancer requiring unplanned medical ICU admission: A retrospective multicenter studyG Kemoun, E Weiss, L El Houari, et al.
Brain Pathology (Zurich, Switzerland)|April 24, 2020
Investigating the presence of doubly phosphorylated α-synuclein at tyrosine 125 and serine 129 in idiopathic Lewy body diseasesMuneera Fayyad, Daniel Erskine, Nour K Majbour, et al.
DNA Repair|March 4, 2006
The nuclear accumulation of the Fanconi anemia protein FANCE depends on FANCCFrance Léveillé, Miriam Ferrer, Annette L Medhurst, et al.
Journal of Thrombosis and Thrombolysis|December 8, 2023
The association of tumor-expressed REG4, SPINK4 and alpha-1 antitrypsin with cancer-associated thrombosis in colorectal cancerJeroen T Buijs, Robin van Beijnum, Rayna J S Anijs, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Dysspondyloenchondromatosis without COL2A1 mutation: possible genetic heterogeneityFrédéric Tran Mau-Them, Aurélia Boualam, Mouna Barat-Houari, et al.
Blood|May 25, 2006
Evidence for subcomplexes in the Fanconi anemia pathwayAnnette L Medhurst, El Houari Laghmani, Jurgen Steltenpool, et al.
European Journal of Medical Genetics|February 26, 2023
Association of Meier-Gorlin and microcephalic osteodysplastic primordial dwarfism type II clinical features in an individual with CDK5RAP2 primary microcephalyQuentin Sabbagh, Mylène Tharreau, Camille Cenni, et al.
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