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Journal of Inherited Metabolic Disease|June 4, 2010
Cystic fibrosis newborn screening: using experience to optimize the screening algorithmJaime E Hale, Richard B Parad, Henry L Dorkin, et al.Clinical and Diagnostic Laboratory Immunology|September 11, 2004
Interleukin 8 secretion from monocytes of subjects heterozygous for the deltaF508 cystic fibrosis transmembrane conductance regulator gene mutation is alteredMunir M Zaman, Andres Gelrud, Omer Junaidi, et al.Contemporary Clinical Trials|July 30, 2022
Protocol for the Vitamin D Oral Replacement in Asthma (VDORA) studyLaura James, Brian P O'Sullivan, Mark Majure, et al.Chest|July 7, 2011
Burkholderia pseudomallei infection in a child with cystic fibrosis: acquisition in the Western HemisphereBrian P O'Sullivan, Brenda Torres, Giuseppe Conidi, et al.Pediatric Pulmonology|September 15, 2020
Obesity-related asthma in children: A role for vitamin DBrian P O'Sullivan, Laura James, Joseph M Majure, et al.Respiratory Care|March 31, 2009
Cystic fibrosis pulmonary guidelines: airway clearance therapiesPatrick A Flume, Karen A Robinson, Brian P O'Sullivan, et al.Blood|February 12, 2005
Platelet activation in cystic fibrosisBrian P O'Sullivan, Matthew D Linden, Andrew L Frelinger, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 15, 2024
Self-reported chronic therapy use after 24-weeks of follow-up by participants who completed the simplify randomized, controlled trialAlex H Gifford, Katherine Odem-Davis, Margaret Kloster, et al.The New England Journal of Medicine|February 6, 2004
Association of cystic fibrosis with abnormalities in fatty acid metabolismSteven D Freedman, Paola G Blanco, Munir M Zaman, et al.Pediatrics|February 3, 2007
Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop reportAnne Marie Comeau, Frank J Accurso, Terry B White, et al.Pageof 4