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Mary Corey

Showing results (51-60 of 72) with videos related to

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The Journal of Pediatrics|February 14, 2003
Glucose intolerance in children with cystic fibrosisMelinda P Solomon, David C Wilson, Mary Corey, et al.
American Journal of Respiratory and Critical Care Medicine|November 17, 2007
Reference ranges for spirometry across all ages: a new approachSanja Stanojevic, Angie Wade, Janet Stocks, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 8, 2022
Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variantsKaren S Raraigh, Michelle H Lewis, Joseph M Collaco, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 27, 2014
European Cystic Fibrosis Society Standards of Care: Quality Management in cystic fibrosisMartin Stern, Dominique Pougheon Bertrand, Elisabetta Bignamini, et al.
The European Respiratory Journal|November 2, 2013
Longitudinal relationship between physical activity and lung health in patients with cystic fibrosisJane E Schneiderman, Donna L Wilkes, Eshetu G Atenafu, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|November 11, 2006
Long-term docosahexaenoic acid therapy in a congenic murine model of cystic fibrosisSatti Beharry, Cameron Ackerley, Mary Corey, et al.
Gastroenterology|October 7, 2010
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosisChee Y Ooi, Ruslan Dorfman, Marco Cipolli, et al.
Thorax|October 24, 2013
Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?Chee Y Ooi, Annie Dupuis, Lynda Ellis, et al.
The Journal of Clinical Investigation|February 23, 2008
Complex two-gene modulation of lung disease severity in children with cystic fibrosisRuslan Dorfman, Andrew Sandford, Chelsea Taylor, et al.
Annals of the American Thoracic Society|April 5, 2014
Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?Chee Y Ooi, Annie Dupuis, Tanja Gonska, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
The Journal of Pediatrics|February 14, 2003
Glucose intolerance in children with cystic fibrosisMelinda P Solomon, David C Wilson, Mary Corey, et al.
American Journal of Respiratory and Critical Care Medicine|November 17, 2007
Reference ranges for spirometry across all ages: a new approachSanja Stanojevic, Angie Wade, Janet Stocks, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 8, 2022
Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variantsKaren S Raraigh, Michelle H Lewis, Joseph M Collaco, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 27, 2014
European Cystic Fibrosis Society Standards of Care: Quality Management in cystic fibrosisMartin Stern, Dominique Pougheon Bertrand, Elisabetta Bignamini, et al.
The European Respiratory Journal|November 2, 2013
Longitudinal relationship between physical activity and lung health in patients with cystic fibrosisJane E Schneiderman, Donna L Wilkes, Eshetu G Atenafu, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|November 11, 2006
Long-term docosahexaenoic acid therapy in a congenic murine model of cystic fibrosisSatti Beharry, Cameron Ackerley, Mary Corey, et al.
Gastroenterology|October 7, 2010
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosisChee Y Ooi, Ruslan Dorfman, Marco Cipolli, et al.
Thorax|October 24, 2013
Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?Chee Y Ooi, Annie Dupuis, Lynda Ellis, et al.
The Journal of Clinical Investigation|February 23, 2008
Complex two-gene modulation of lung disease severity in children with cystic fibrosisRuslan Dorfman, Andrew Sandford, Chelsea Taylor, et al.
Annals of the American Thoracic Society|April 5, 2014
Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?Chee Y Ooi, Annie Dupuis, Tanja Gonska, et al.
Pageof 8