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Matthias Griese

Showing results (171-180 of 280) with videos related to

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ERJ Open Research|July 31, 2019
Bi-allelic missense <i>ABCA3</i> mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Orphanet Journal of Rare Diseases|March 28, 2018
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhoodMeike Hengst, Lutz Naehrlich, Poornima Mahavadi, et al.
Trials|September 15, 2022
Identifying obstacles hindering the conduct of academic-sponsored trials for drug repurposing on rare-diseases: an analysis of six use casesMarta Del Álamo, Christoph Bührer, Dirk Fisher, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 20, 2008
Infiltrated neutrophils acquire novel chemokine receptor expression and chemokine responsiveness in chronic inflammatory lung diseasesDominik Hartl, Susanne Krauss-Etschmann, Barbara Koller, et al.
Canadian Respiratory Journal|February 21, 2020
Postinfectious Bronchiolitis Obliterans in Children: Diagnostic Workup and Therapeutic Options: A Workshop ReportSilvija-Pera Jerkic, Folke Brinkmann, Alistair Calder, et al.
Breathe (Sheffield, England)|May 14, 2025
An update on diagnosis and treatments of childhood interstitial lung diseasesHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 15, 2011
Ultrastructural characterization of cystic fibrosis sputum using atomic force and scanning electron microscopyReinhard Manzenreiter, Ferry Kienberger, Veronica Marcos, et al.
Pediatric Pulmonology|December 16, 2011
Feasibility and variability of measuring the Lung Clearance Index in a multi-center settingSusanne I Fuchs, Helmut Ellemunter, Johannes Eder, et al.
Plos One|June 24, 2016
Serum Levels of Surfactant Proteins in Patients with Combined Pulmonary Fibrosis and Emphysema (CPFE)Andriana I Papaioannou, Konstantinos Kostikas, Effrosyni D Manali, et al.
The Lancet. Respiratory Medicine|October 15, 2014
Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST)Edward F McKone, Drucy Borowitz, Pavel Drevinek, et al.
Pageof 28

Showing results (171-180 of 280) with videos related to

Sort By:
Pageof 28
ERJ Open Research|July 31, 2019
Bi-allelic missense <i>ABCA3</i> mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Orphanet Journal of Rare Diseases|March 28, 2018
Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhoodMeike Hengst, Lutz Naehrlich, Poornima Mahavadi, et al.
Trials|September 15, 2022
Identifying obstacles hindering the conduct of academic-sponsored trials for drug repurposing on rare-diseases: an analysis of six use casesMarta Del Álamo, Christoph Bührer, Dirk Fisher, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 20, 2008
Infiltrated neutrophils acquire novel chemokine receptor expression and chemokine responsiveness in chronic inflammatory lung diseasesDominik Hartl, Susanne Krauss-Etschmann, Barbara Koller, et al.
Canadian Respiratory Journal|February 21, 2020
Postinfectious Bronchiolitis Obliterans in Children: Diagnostic Workup and Therapeutic Options: A Workshop ReportSilvija-Pera Jerkic, Folke Brinkmann, Alistair Calder, et al.
Breathe (Sheffield, England)|May 14, 2025
An update on diagnosis and treatments of childhood interstitial lung diseasesHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 15, 2011
Ultrastructural characterization of cystic fibrosis sputum using atomic force and scanning electron microscopyReinhard Manzenreiter, Ferry Kienberger, Veronica Marcos, et al.
Pediatric Pulmonology|December 16, 2011
Feasibility and variability of measuring the Lung Clearance Index in a multi-center settingSusanne I Fuchs, Helmut Ellemunter, Johannes Eder, et al.
Plos One|June 24, 2016
Serum Levels of Surfactant Proteins in Patients with Combined Pulmonary Fibrosis and Emphysema (CPFE)Andriana I Papaioannou, Konstantinos Kostikas, Effrosyni D Manali, et al.
The Lancet. Respiratory Medicine|October 15, 2014
Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST)Edward F McKone, Drucy Borowitz, Pavel Drevinek, et al.
Pageof 28