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Biorxiv : the Preprint Server for Biology|June 22, 2026
Perturbation of genes linked to common schizophrenia risk variants identifies cilia programsJiseok Lee, Hyunggyu Min, Cristine Casingal, et al.The Journal of Asthma : Official Journal of the Association for the Care of Asthma|August 15, 2019
Weighing in on asthma: Insights on BMI, magnesium, and hospitalizations from the Ohio Pediatric Asthma RepositoryChristine L Schuler, Jocelyn M Biagini Myers, Carolyn M Kercsmar, et al.Cancer Medicine|December 31, 2020
A phase II trial of durvalumab and tremelimumab in metastatic, non-urothelial carcinoma of the urinary tractMichal Sarfaty, Karissa Whiting, Min Yuen Teo, et al.Pediatrics|January 21, 2015
Heterogeneity in asthma care in a statewide collaborative: the Ohio Pediatric Asthma RepositoryJocelyn M Biagini Myers, Jeffrey M Simmons, Carolyn M Kercsmar, et al.Lancet (London, England)|August 3, 2024
Safety and efficacy of subcutaneous iscalimab (CFZ533) in two distinct populations of patients with Sjögren's disease (TWINSS): week 24 results of a randomised, double-blind, placebo-controlled, phase 2b dose-ranging studyBenjamin A Fisher, Xavier Mariette, Athena Papas, et al.Conservation Physiology|February 23, 2026
Embryos are largely understudied in a representative sample of journals in conservation physiologyPatrice Pottier, Nicholas C Wu, Madison L Earhart, et al.American Journal of Respiratory and Critical Care Medicine|April 25, 2018
Effects of an Antioxidant-enriched Multivitamin in Cystic Fibrosis. A Randomized, Controlled, Multicenter Clinical TrialScott D Sagel, Umer Khan, Raksha Jain, et al.Seminars in Arthritis and Rheumatism|June 11, 2026
OMERACT- determining a core domain set for Sjögren's disease: International focus group seriesDana D DiRenzo, Lee Ang, Caroline O'Brien, et al.Hospital Pediatrics|May 17, 2018
Ohio Pediatric Asthma Repository: Opportunities to Revise Care Practices to Decrease Time to Physiologic Readiness for DischargeJeffrey M Simmons, Jocelyn M Biagini Myers, Lisa J Martin, et al.Cancer Research|November 4, 2015
A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal EvolutionKyle M Walsh, Adam J de Smith, Helen M Hansen, et al.Pageof 67