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Felix Ratjen

Showing results (191-200 of 326) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 29, 2019
Lavage lipidomics signatures in children with cystic fibrosis and protracted bacterial bronchitisElias Seidl, Hannah Kiermeier, Gerhard Liebisch, et al.
Orphanet Journal of Rare Diseases|November 10, 2024
Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasiaLauren A Beslow, Helen Kim, Steven W Hetts, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 1, 2024
Assessing <sup>129</sup>Xe multi-breath washout MRI response to elexacaftor/tezacaftor/ivacaftor intervention in pediatric CFFaiyza Alam, Samal Munidasa, Brandon Zanette, et al.
Thorax|April 16, 2022
Evaluation of clinically relevant changes in the lung clearance index in children with cystic fibrosis and healthy controlsLucy Perrem, Sanja Stanojevic, Melinda Solomon, et al.
Academic Radiology|June 14, 2020
Comparison of Functional Free-Breathing Pulmonary <sup>1</sup>H and Hyperpolarized <sup>129</sup>Xe Magnetic Resonance Imaging in Pediatric Cystic FibrosisMarcus J Couch, Samal Munidasa, Jonathan H Rayment, et al.
Paediatric Respiratory Reviews|August 5, 2009
Exercise and physical activity in children with cystic fibrosisDonna L Wilkes, Jane E Schneiderman, Thanh Nguyen, et al.
Pediatric Pulmonology|March 3, 2011
Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: short-term tolerability, adherence, and safetyMargaret Rosenfeld, Stephanie Davis, Lyndia Brumback, et al.
The Lancet. Respiratory Medicine|January 31, 2021
Long-term safety and efficacy of lumacaftor-ivacaftor therapy in children aged 6-11 years with cystic fibrosis homozygous for the F508del-CFTR mutation: a phase 3, open-label, extension studyMark A Chilvers, Jane C Davies, Carlos Milla, et al.
Pediatric Pulmonology|July 11, 2025
Repeatability of Multiple Breath Washout in Pediatric Primary Ciliary DyskinesiaWallace B Wee, Layan M Bashi, Renee Jensen, et al.
Thorax|February 15, 2013
Long-term multicentre randomised controlled study of high frequency chest wall oscillation versus positive expiratory pressure mask in cystic fibrosisMaggie Patricia McIlwaine, Nancy Alarie, George F Davidson, et al.
Pageof 33

Showing results (191-200 of 326) with videos related to

Sort By:
Pageof 33
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 29, 2019
Lavage lipidomics signatures in children with cystic fibrosis and protracted bacterial bronchitisElias Seidl, Hannah Kiermeier, Gerhard Liebisch, et al.
Orphanet Journal of Rare Diseases|November 10, 2024
Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasiaLauren A Beslow, Helen Kim, Steven W Hetts, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 1, 2024
Assessing <sup>129</sup>Xe multi-breath washout MRI response to elexacaftor/tezacaftor/ivacaftor intervention in pediatric CFFaiyza Alam, Samal Munidasa, Brandon Zanette, et al.
Thorax|April 16, 2022
Evaluation of clinically relevant changes in the lung clearance index in children with cystic fibrosis and healthy controlsLucy Perrem, Sanja Stanojevic, Melinda Solomon, et al.
Academic Radiology|June 14, 2020
Comparison of Functional Free-Breathing Pulmonary <sup>1</sup>H and Hyperpolarized <sup>129</sup>Xe Magnetic Resonance Imaging in Pediatric Cystic FibrosisMarcus J Couch, Samal Munidasa, Jonathan H Rayment, et al.
Paediatric Respiratory Reviews|August 5, 2009
Exercise and physical activity in children with cystic fibrosisDonna L Wilkes, Jane E Schneiderman, Thanh Nguyen, et al.
Pediatric Pulmonology|March 3, 2011
Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: short-term tolerability, adherence, and safetyMargaret Rosenfeld, Stephanie Davis, Lyndia Brumback, et al.
The Lancet. Respiratory Medicine|January 31, 2021
Long-term safety and efficacy of lumacaftor-ivacaftor therapy in children aged 6-11 years with cystic fibrosis homozygous for the F508del-CFTR mutation: a phase 3, open-label, extension studyMark A Chilvers, Jane C Davies, Carlos Milla, et al.
Pediatric Pulmonology|July 11, 2025
Repeatability of Multiple Breath Washout in Pediatric Primary Ciliary DyskinesiaWallace B Wee, Layan M Bashi, Renee Jensen, et al.
Thorax|February 15, 2013
Long-term multicentre randomised controlled study of high frequency chest wall oscillation versus positive expiratory pressure mask in cystic fibrosisMaggie Patricia McIlwaine, Nancy Alarie, George F Davidson, et al.
Pageof 33