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Margaret L Salisbury

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Clinics in Chest Medicine|May 24, 2021
Management of Idiopathic Pulmonary FibrosisMargaret L Salisbury, Marlies S Wijsenbeek
Chest|February 20, 2021
Identification and Remediation of Environmental Exposures in Patients With Interstitial Lung Disease: Evidence Review and Practical ConsiderationsCarla R Copeland, Bridget F Collins, Margaret L Salisbury
Current Opinion in Pulmonary Medicine|June 27, 2017
Microbiome in interstitial lung disease: from pathogenesis to treatment targetMargaret L Salisbury, MeiLan K Han, Robert P Dickson, et al.
American Journal of Respiratory and Critical Care Medicine|February 25, 2026
Identification of a conserved sequence of disease progression in Idiopathic Pulmonary FibrosisXiang Huang, Pingsheng Wu, Adam R Guttentag, et al.
American Journal of Respiratory and Critical Care Medicine|August 13, 2024
Progressive Early Interstitial Lung Abnormalities in Persons at Risk for Familial Pulmonary Fibrosis: A Prospective Cohort StudyMargaret L Salisbury, Cheryl Markin, Tisra Fadely, et al.
Respiratory Medicine|September 1, 2016
Predictors of idiopathic pulmonary fibrosis in absence of radiologic honeycombing: A cross sectional analysis in ILD patients undergoing lung tissue samplingMargaret L Salisbury, Meng Xia, Susan Murray, et al.
BMJ Open Respiratory Research|May 16, 2024
Scoping review of exposure questionnaires and surveys in interstitial lung diseaseHayley Barnes, Seham Elmrayed, Christopher Michael Barber, et al.
Annals of the American Thoracic Society|June 24, 2020
Antifibrotic Drug Use in Patients with Idiopathic Pulmonary Fibrosis. Data from the IPF-PRO RegistryMargaret L Salisbury, Craig S Conoscenti, Daniel A Culver, et al.
Chest|October 2, 2015
Idiopathic Pulmonary Fibrosis: Gender-Age-Physiology Index Stage for Predicting Future Lung Function DeclineMargaret L Salisbury, Meng Xia, Yueren Zhou, et al.
Lung|September 6, 2024
Utility of the 52-Gene Risk Score to Identify Patients with Idiopathic Pulmonary Fibrosis at Greater Risk of Mortality in the Era of Antifibrotic TherapyJulia F Söllner, Stefan Bentink, Christian Hesslinger, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Clinics in Chest Medicine|May 24, 2021
Management of Idiopathic Pulmonary FibrosisMargaret L Salisbury, Marlies S Wijsenbeek
Chest|February 20, 2021
Identification and Remediation of Environmental Exposures in Patients With Interstitial Lung Disease: Evidence Review and Practical ConsiderationsCarla R Copeland, Bridget F Collins, Margaret L Salisbury
Current Opinion in Pulmonary Medicine|June 27, 2017
Microbiome in interstitial lung disease: from pathogenesis to treatment targetMargaret L Salisbury, MeiLan K Han, Robert P Dickson, et al.
American Journal of Respiratory and Critical Care Medicine|February 25, 2026
Identification of a conserved sequence of disease progression in Idiopathic Pulmonary FibrosisXiang Huang, Pingsheng Wu, Adam R Guttentag, et al.
American Journal of Respiratory and Critical Care Medicine|August 13, 2024
Progressive Early Interstitial Lung Abnormalities in Persons at Risk for Familial Pulmonary Fibrosis: A Prospective Cohort StudyMargaret L Salisbury, Cheryl Markin, Tisra Fadely, et al.
Respiratory Medicine|September 1, 2016
Predictors of idiopathic pulmonary fibrosis in absence of radiologic honeycombing: A cross sectional analysis in ILD patients undergoing lung tissue samplingMargaret L Salisbury, Meng Xia, Susan Murray, et al.
BMJ Open Respiratory Research|May 16, 2024
Scoping review of exposure questionnaires and surveys in interstitial lung diseaseHayley Barnes, Seham Elmrayed, Christopher Michael Barber, et al.
Annals of the American Thoracic Society|June 24, 2020
Antifibrotic Drug Use in Patients with Idiopathic Pulmonary Fibrosis. Data from the IPF-PRO RegistryMargaret L Salisbury, Craig S Conoscenti, Daniel A Culver, et al.
Chest|October 2, 2015
Idiopathic Pulmonary Fibrosis: Gender-Age-Physiology Index Stage for Predicting Future Lung Function DeclineMargaret L Salisbury, Meng Xia, Yueren Zhou, et al.
Lung|September 6, 2024
Utility of the 52-Gene Risk Score to Identify Patients with Idiopathic Pulmonary Fibrosis at Greater Risk of Mortality in the Era of Antifibrotic TherapyJulia F Söllner, Stefan Bentink, Christian Hesslinger, et al.
Pageof 3