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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.
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