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Frontiers in Immunology|October 20, 2022
MIS-C: A COVID-19-as sociated condition between hypoimmunity and hyperimmunityMonica Gelzo, Alice Castaldo, Antonietta Giannattasio, et al.Iscience|June 3, 2026
Red blood cell deformability as a mechanobiological marker of CFTR dysfunction in cystic fibrosisEleonora Pero, Giovanna Tomaiuolo, Valeria Rachela Villella, et al.Pediatric Pulmonology|September 22, 2021
Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/CF screen-positive, inconclusive diagnosisVito Terlizzi, Laura Claut, Carla Colombo, et al.Cell Death & Disease|March 16, 2019
Autophagy suppresses the pathogenic immune response to dietary antigens in cystic fibrosisValeria R Villella, Speranza Esposito, Eleonora Ferrari, et al.Journal of Bronchology & Interventional Pulmonology|June 14, 2022
The Role of Bronchoscopy in the Management of Children With Cystic FibrosisAntonella Tosco, Piercarlo Poli, Alida Casale, et al.Aging|April 14, 2019
Genistein antagonizes gliadin-induced CFTR malfunction in models of celiac diseaseSperanza Esposito, Valeria Rachela Villella, Eleonora Ferrari, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 22, 2021
A survey of the prevalence, management and outcome of infants with an inconclusive diagnosis following newborn bloodspot screening for cystic fibrosis (CRMS/CFSPID) in six Italian centresVito Terlizzi, Laura Claut, Antonella Tosco, et al.The Journal of Pediatrics|June 30, 2024
Reported Adverse Events in a Multicenter Cohort of Patients Ages 6-18 Years with Cystic Fibrosis and at Least One F508del Allele Receiving Elexacaftor/Tezacaftor/IvacaftorVito Terlizzi, Cristina Fevola, Santiago Presti, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 6, 2022
Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotypeAntonella Tosco, Alice Castaldo, Carla Colombo, et al.Pageof 4