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Matthias Griese

Showing results (181-190 of 280) with videos related to

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American Journal of Physiology. Lung Cellular and Molecular Physiology|February 20, 2024
Multivalent, calcium-independent binding of surfactant protein A and D to sulfated glycosaminoglycans of the alveolar epithelial glycocalyxRabia Avcibas, Anna Vermul, Vladimir Gluhovic, et al.
Pediatric Pulmonology|January 30, 2024
Estimating the effect of nintedanib on forced vital capacity in children and adolescents with fibrosing interstitial lung disease using a Bayesian dynamic borrowing approachToby M Maher, Kevin K Brown, Steven Cunningham, et al.
Respiratory Medicine|June 15, 2016
Lung clearance index for monitoring early lung disease in alpha-1-antitrypsin deficiencySusanne I Fuchs, Nicolaus Schwerk, Klaus Pittschieler, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 10, 2016
Microbial colonization and lung function in adolescents with cystic fibrosisAndreas Hector, Tobias Kirn, Anjali Ralhan, et al.
Thorax|February 12, 2022
Healthcare resource utilisation and medical costs for children with interstitial lung diseases (chILD) in EuropeElias Seidl, Nicolaus Schwerk, Julia Carlens, et al.
Pediatric Pulmonology|June 22, 2026
Continued Nintedanib Treatment in Children and Adolescents With Fibrosing ILDs: Data From InPedILD-ONRobin Deterding, Lisa R Young, Emily M DeBoer, et al.
Klinische Padiatrie|January 3, 2022
Interventional Bronchus Occlusion Using Amplatzer Devices - A Promising Treatment Option for Children with Persistent Air LeakKatharina Schütz, Christoph M Happel, Oliver Keil, et al.
BMC Pediatrics|August 19, 2011
Long-term follow-up and treatment of congenital alveolar proteinosisMatthias Griese, Jan Ripper, Anke Sibbersen, et al.
American Journal of Respiratory and Critical Care Medicine|May 27, 2006
Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiencyFrank Brasch, Sven Schimanski, Christian Mühlfeld, et al.
The European Respiratory Journal|August 30, 2022
Nintedanib in children and adolescents with fibrosing interstitial lung diseasesRobin Deterding, Lisa R Young, Emily M DeBoer, et al.
Pageof 28

Showing results (181-190 of 280) with videos related to

Sort By:
Pageof 28
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 20, 2024
Multivalent, calcium-independent binding of surfactant protein A and D to sulfated glycosaminoglycans of the alveolar epithelial glycocalyxRabia Avcibas, Anna Vermul, Vladimir Gluhovic, et al.
Pediatric Pulmonology|January 30, 2024
Estimating the effect of nintedanib on forced vital capacity in children and adolescents with fibrosing interstitial lung disease using a Bayesian dynamic borrowing approachToby M Maher, Kevin K Brown, Steven Cunningham, et al.
Respiratory Medicine|June 15, 2016
Lung clearance index for monitoring early lung disease in alpha-1-antitrypsin deficiencySusanne I Fuchs, Nicolaus Schwerk, Klaus Pittschieler, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 10, 2016
Microbial colonization and lung function in adolescents with cystic fibrosisAndreas Hector, Tobias Kirn, Anjali Ralhan, et al.
Thorax|February 12, 2022
Healthcare resource utilisation and medical costs for children with interstitial lung diseases (chILD) in EuropeElias Seidl, Nicolaus Schwerk, Julia Carlens, et al.
Pediatric Pulmonology|June 22, 2026
Continued Nintedanib Treatment in Children and Adolescents With Fibrosing ILDs: Data From InPedILD-ONRobin Deterding, Lisa R Young, Emily M DeBoer, et al.
Klinische Padiatrie|January 3, 2022
Interventional Bronchus Occlusion Using Amplatzer Devices - A Promising Treatment Option for Children with Persistent Air LeakKatharina Schütz, Christoph M Happel, Oliver Keil, et al.
BMC Pediatrics|August 19, 2011
Long-term follow-up and treatment of congenital alveolar proteinosisMatthias Griese, Jan Ripper, Anke Sibbersen, et al.
American Journal of Respiratory and Critical Care Medicine|May 27, 2006
Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiencyFrank Brasch, Sven Schimanski, Christian Mühlfeld, et al.
The European Respiratory Journal|August 30, 2022
Nintedanib in children and adolescents with fibrosing interstitial lung diseasesRobin Deterding, Lisa R Young, Emily M DeBoer, et al.
Pageof 28