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Matthias Griese

Showing results (261-270 of 280) with videos related to

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Blood|February 14, 2013
The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2Birthe Jessen, Sebastian F N Bode, Sandra Ammann, et al.
Thorax|October 24, 2017
International management platform for children's interstitial lung disease (chILD-EU)Matthias Griese, Elias Seidl, Meike Hengst, et al.
Science Immunology|June 19, 2021
Heterozygous <i>OAS1</i> gain-of-function variants cause an autoinflammatory immunodeficiencyThomas Magg, Tsubasa Okano, Lars M Koenig, et al.
American Journal of Human Genetics|July 7, 2018
Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational FunctionZhiwen Xu, Wing-Sze Lo, David B Beck, et al.
ERJ Open Research|April 27, 2023
Diffuse alveolar haemorrhage in children: an international multicentre studyAstrid Madsen Ring, Nicolaus Schwerk, Nural Kiper, et al.
The Lancet. Respiratory Medicine|June 24, 2026
Prevalence and disease trajectories of pulmonary fibrosis of childhood interstitial lung disease: a register-based, multicentre observational studyMatthias Griese, Simone Reu-Hofer, Julia Ley-Zaporozhan, et al.
American Journal of Human Genetics|June 8, 2026
Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorderSock Hoai Chan, Audra N Iness, Jill A Rosenfeld, et al.
Thorax|February 22, 2023
ABCA3-related interstitial lung disease beyond infancyYang Li, Elias Seidl, Katrin Knoflach, et al.
American Journal of Human Genetics|April 2, 2019
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial DysmorphismIllja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.
ERJ Open Research|January 5, 2023
COVID-19 in patients with pulmonary alveolar proteinosis: a European multicentre studySpyros A Papiris, Ilaria Campo, Francesca Mariani, et al.
Pageof 28

Showing results (261-270 of 280) with videos related to

Sort By:
Pageof 28
Blood|February 14, 2013
The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2Birthe Jessen, Sebastian F N Bode, Sandra Ammann, et al.
Thorax|October 24, 2017
International management platform for children's interstitial lung disease (chILD-EU)Matthias Griese, Elias Seidl, Meike Hengst, et al.
Science Immunology|June 19, 2021
Heterozygous <i>OAS1</i> gain-of-function variants cause an autoinflammatory immunodeficiencyThomas Magg, Tsubasa Okano, Lars M Koenig, et al.
American Journal of Human Genetics|July 7, 2018
Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational FunctionZhiwen Xu, Wing-Sze Lo, David B Beck, et al.
ERJ Open Research|April 27, 2023
Diffuse alveolar haemorrhage in children: an international multicentre studyAstrid Madsen Ring, Nicolaus Schwerk, Nural Kiper, et al.
The Lancet. Respiratory Medicine|June 24, 2026
Prevalence and disease trajectories of pulmonary fibrosis of childhood interstitial lung disease: a register-based, multicentre observational studyMatthias Griese, Simone Reu-Hofer, Julia Ley-Zaporozhan, et al.
American Journal of Human Genetics|June 8, 2026
Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorderSock Hoai Chan, Audra N Iness, Jill A Rosenfeld, et al.
Thorax|February 22, 2023
ABCA3-related interstitial lung disease beyond infancyYang Li, Elias Seidl, Katrin Knoflach, et al.
American Journal of Human Genetics|April 2, 2019
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial DysmorphismIllja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.
ERJ Open Research|January 5, 2023
COVID-19 in patients with pulmonary alveolar proteinosis: a European multicentre studySpyros A Papiris, Ilaria Campo, Francesca Mariani, et al.
Pageof 28