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Matthias Griese

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American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
Respirology (Carlton, Vic.)|June 2, 2022
Genetic testing in interstitial lung disease: An international surveyMichelle Terwiel, Raphael Borie, Bruno Crestani, et al.
ERJ Open Research|June 24, 2021
Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung diseaseRobin Deterding, Matthias Griese, Gail Deutsch, et al.
The New England Journal of Medicine|November 4, 2011
A CFTR potentiator in patients with cystic fibrosis and the G551D mutationBonnie W Ramsey, Jane Davies, N Gerard McElvaney, et al.
The European Respiratory Journal|August 15, 2024
European Respiratory Society guidelines for the diagnosis and management of pulmonary alveolar proteinosisCormac McCarthy, Francesco Bonella, Marissa O'Callaghan, et al.
ERJ Open Research|March 30, 2022
Autoimmune pulmonary alveolar proteinosis in childrenMatthias Griese, Panagiota Panagiotou, Effrosyni D Manali, et al.
Thorax|November 22, 2019
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD)Steve Cunningham, Catriona Graham, Morag MacLean, et al.
The European Respiratory Journal|February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.
Genetics in Medicine Open|January 17, 2024
Biallelic variants in the calpain regulatory subunit <i>CAPNS1</i> cause pulmonary arterial hypertensionAlex V Postma, Christina K Rapp, Katrin Knoflach, et al.
Frontiers in Immunology|October 24, 2022
Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported casesRensheng Wan, Johannes Fänder, Ia Zakaraia, et al.
Pageof 28

Showing results (231-240 of 280) with videos related to

Sort By:
Pageof 28
American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
Respirology (Carlton, Vic.)|June 2, 2022
Genetic testing in interstitial lung disease: An international surveyMichelle Terwiel, Raphael Borie, Bruno Crestani, et al.
ERJ Open Research|June 24, 2021
Study design of a randomised, placebo-controlled trial of nintedanib in children and adolescents with fibrosing interstitial lung diseaseRobin Deterding, Matthias Griese, Gail Deutsch, et al.
The New England Journal of Medicine|November 4, 2011
A CFTR potentiator in patients with cystic fibrosis and the G551D mutationBonnie W Ramsey, Jane Davies, N Gerard McElvaney, et al.
The European Respiratory Journal|August 15, 2024
European Respiratory Society guidelines for the diagnosis and management of pulmonary alveolar proteinosisCormac McCarthy, Francesco Bonella, Marissa O'Callaghan, et al.
ERJ Open Research|March 30, 2022
Autoimmune pulmonary alveolar proteinosis in childrenMatthias Griese, Panagiota Panagiotou, Effrosyni D Manali, et al.
Thorax|November 22, 2019
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD)Steve Cunningham, Catriona Graham, Morag MacLean, et al.
The European Respiratory Journal|February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.
Genetics in Medicine Open|January 17, 2024
Biallelic variants in the calpain regulatory subunit <i>CAPNS1</i> cause pulmonary arterial hypertensionAlex V Postma, Christina K Rapp, Katrin Knoflach, et al.
Frontiers in Immunology|October 24, 2022
Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported casesRensheng Wan, Johannes Fänder, Ia Zakaraia, et al.
Pageof 28