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Wim Wuyts

Showing results (91-100 of 135) with videos related to

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Cancer Research|October 20, 2021
Patterns of Carbon-Bound Exogenous Compounds in Patients with Lung Cancer and Association with Disease PathophysiologyThomas Kunzke, Verena M Prade, Achim Buck, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 19, 2025
Epigenetic age acceleration in idiopathic pulmonary fibrosis revealed by DNA methylation clocksDaniel B Kurbanov, Farida Ahangari, Taylor Adams, et al.
Respiratory Research|February 28, 2025
Person-centred health outcomes in the routine care for people with progressive pulmonary fibrosis: the COCOS-IPF project's European survey on healthcare professionals' views and practicesVivien Somogyi, Anouk Delameillieure, Silja Schenk, et al.
ERJ Open Research|March 18, 2026
The COCOS-IPF core outcome set for idiopathic pulmonary fibrosis/progressive pulmonary fibrosis care: a mixed-method multi-perspective approachSofie Breuls, Vivien Somogyi, Silja Schenk, et al.
RMD Open|February 26, 2025
Lung ultrasound outperforms symptom-based screening to detect interstitial lung disease associated with rheumatoid arthritisMarie Vermant, Alexandros Kalkanis, Joseph Jacob, et al.
ERJ Open Research|March 26, 2024
ERS International Congress 2023: highlights from the Interstitial Lung Diseases AssemblyLaura Fabbri, Julien Guiot, Marie Vermant, et al.
Haematologica|July 14, 2018
The <i>SLC40A1</i> R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanismChandran Ka, Julie Guellec, Xavier Pepermans, et al.
Molecular Genetics & Genomic Medicine|January 12, 2019
RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromasGavin R Oliver, Patrick R Blackburn, Marissa S Ellingson, et al.
Human Mutation|April 25, 2015
Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm GenesDorien Proost, Geert Vandeweyer, Josephina A N Meester, et al.
BMJ Open Respiratory Research|April 9, 2019
First patient-centred set of outcomes for pulmonary sarcoidosis: a multicentre initiativeNynke A Kampstra, Jan C Grutters, Frouke T van Beek, et al.
Pageof 14

Showing results (91-100 of 135) with videos related to

Sort By:
Pageof 14
Cancer Research|October 20, 2021
Patterns of Carbon-Bound Exogenous Compounds in Patients with Lung Cancer and Association with Disease PathophysiologyThomas Kunzke, Verena M Prade, Achim Buck, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 19, 2025
Epigenetic age acceleration in idiopathic pulmonary fibrosis revealed by DNA methylation clocksDaniel B Kurbanov, Farida Ahangari, Taylor Adams, et al.
Respiratory Research|February 28, 2025
Person-centred health outcomes in the routine care for people with progressive pulmonary fibrosis: the COCOS-IPF project's European survey on healthcare professionals' views and practicesVivien Somogyi, Anouk Delameillieure, Silja Schenk, et al.
ERJ Open Research|March 18, 2026
The COCOS-IPF core outcome set for idiopathic pulmonary fibrosis/progressive pulmonary fibrosis care: a mixed-method multi-perspective approachSofie Breuls, Vivien Somogyi, Silja Schenk, et al.
RMD Open|February 26, 2025
Lung ultrasound outperforms symptom-based screening to detect interstitial lung disease associated with rheumatoid arthritisMarie Vermant, Alexandros Kalkanis, Joseph Jacob, et al.
ERJ Open Research|March 26, 2024
ERS International Congress 2023: highlights from the Interstitial Lung Diseases AssemblyLaura Fabbri, Julien Guiot, Marie Vermant, et al.
Haematologica|July 14, 2018
The <i>SLC40A1</i> R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanismChandran Ka, Julie Guellec, Xavier Pepermans, et al.
Molecular Genetics & Genomic Medicine|January 12, 2019
RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromasGavin R Oliver, Patrick R Blackburn, Marissa S Ellingson, et al.
Human Mutation|April 25, 2015
Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm GenesDorien Proost, Geert Vandeweyer, Josephina A N Meester, et al.
BMJ Open Respiratory Research|April 9, 2019
First patient-centred set of outcomes for pulmonary sarcoidosis: a multicentre initiativeNynke A Kampstra, Jan C Grutters, Frouke T van Beek, et al.
Pageof 14