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The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.Journal of Clinical Psychology in Medical Settings|September 24, 2021
Extending the Common Sense Model to Explore the Impact of the Fear of COVID-19 on Quality of Life in an International Inflammatory Bowel Disease CohortBree Hayes, Pragalathan Apputhurai, Antonina Mikocka-Walus, et al.The Journal of Pediatrics|March 16, 2015
Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic FibrosisMelissa R Miller, David Soave, Weili Li, et al.Annals of the American Thoracic Society|October 9, 2024
Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic FibrosisBreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.Physiological Genomics|December 24, 2009
EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severityRebecca Darrah, Edward McKone, Clare O'Connor, et al.Chest|December 10, 2023
Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary DyskinesiaKimberley R Kaspy, Sharon D Dell, Stephanie D Davis, et al.American Journal of Respiratory and Critical Care Medicine|December 11, 2014
Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotypeStephanie D Davis, Thomas W Ferkol, Margaret Rosenfeld, et al.Pediatric Pulmonology|May 9, 2025
The Association of Neonatal Respiratory Distress With Ciliary Ultrastructure and Genotype in Primary Ciliary DyskinesiaAndrew T Barber, Stephanie D Davis, Thomas W Ferkol, et al.The Journal of Clinical Investigation|July 28, 2022
Small-molecule eRF3a degraders rescue CFTR nonsense mutations by promoting premature termination codon readthroughRhianna E Lee, Catherine A Lewis, Lihua He, et al.Pageof 78