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Pulmonary Circulation
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December 19, 2017
The impact of ambrisentan and tadalafil upfront combination therapy on cardiac function in scleroderma associated pulmonary arterial hypertension patients: cardiac magnetic resonance feature tracking study
Takahiro Sato, Bharath Ambale-Venkatesh, Joao A C Lima, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 12, 2015
Ambrisentan and Tadalafil Up-front Combination Therapy in Scleroderma-associated Pulmonary Arterial Hypertension
Paul M Hassoun, Roham T Zamanian, Rachel Damico, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 13, 2022
Impact of Sex and Gender on Autoimmune Lung Disease: Opportunities for Future Research: NHLBI Working Group Report
Elizabeth R Volkmann, Jill Siegfried, Tim Lahm, et al.
Pulmonary Circulation
|
May 6, 2022
Delphi consensus recommendation for optimization of pulmonary hypertension therapy focusing on switching from a phosphodiesterase 5 inhibitor to riociguat
Franck F Rahaghi, Vijay P Balasubramanian, Robert C Bourge, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 16, 2018
Assessment of Right Ventricular Function in the Research Setting: Knowledge Gaps and Pathways Forward. An Official American Thoracic Society Research Statement
Tim Lahm, Ivor S Douglas, Stephen L Archer, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Resolving Diagnostic Discordance in Group 2 Pulmonary Hypertension Through Staged Physiologic Testing: Insights From PVDOMICS
Franz P Rischard, Mateo Mendoza, Michael Insel, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 10, 2014
Serum endostatin is a genetically determined predictor of survival in pulmonary arterial hypertension
Rachel Damico, Todd M Kolb, Lidenys Valera, et al.
European Heart Journal. Cardiovascular Imaging
|
June 7, 2021
Comprehensive echocardiographic evaluation of the right heart in patients with pulmonary vascular diseases: the PVDOMICS experience
Christine L Jellis, Margaret M Park, Aiden Abidov, et al.
Circulation
|
February 13, 2026
Elevated Pulmonary Artery Wedge Pressure in Group 1 Pulmonary Hypertension
Yogesh N V Reddy, Robert P Frantz, William R Miranda, et al.
Annals of the American Thoracic Society
|
July 18, 2025
Ground Glass Opacities in Pulmonary Arterial Hypertension-Results from the PVDOMICS Study
Divya Padmanabhan Menon, Robert P Frantz, Benjamin R Gochanour, et al.
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of 22
Search research articles
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Showing results (191-200 of 217) with videos related to
Sort By:
Page
of 22
Pulmonary Circulation
|
December 19, 2017
The impact of ambrisentan and tadalafil upfront combination therapy on cardiac function in scleroderma associated pulmonary arterial hypertension patients: cardiac magnetic resonance feature tracking study
Takahiro Sato, Bharath Ambale-Venkatesh, Joao A C Lima, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 12, 2015
Ambrisentan and Tadalafil Up-front Combination Therapy in Scleroderma-associated Pulmonary Arterial Hypertension
Paul M Hassoun, Roham T Zamanian, Rachel Damico, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 13, 2022
Impact of Sex and Gender on Autoimmune Lung Disease: Opportunities for Future Research: NHLBI Working Group Report
Elizabeth R Volkmann, Jill Siegfried, Tim Lahm, et al.
Pulmonary Circulation
|
May 6, 2022
Delphi consensus recommendation for optimization of pulmonary hypertension therapy focusing on switching from a phosphodiesterase 5 inhibitor to riociguat
Franck F Rahaghi, Vijay P Balasubramanian, Robert C Bourge, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 16, 2018
Assessment of Right Ventricular Function in the Research Setting: Knowledge Gaps and Pathways Forward. An Official American Thoracic Society Research Statement
Tim Lahm, Ivor S Douglas, Stephen L Archer, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Resolving Diagnostic Discordance in Group 2 Pulmonary Hypertension Through Staged Physiologic Testing: Insights From PVDOMICS
Franz P Rischard, Mateo Mendoza, Michael Insel, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 10, 2014
Serum endostatin is a genetically determined predictor of survival in pulmonary arterial hypertension
Rachel Damico, Todd M Kolb, Lidenys Valera, et al.
European Heart Journal. Cardiovascular Imaging
|
June 7, 2021
Comprehensive echocardiographic evaluation of the right heart in patients with pulmonary vascular diseases: the PVDOMICS experience
Christine L Jellis, Margaret M Park, Aiden Abidov, et al.
Circulation
|
February 13, 2026
Elevated Pulmonary Artery Wedge Pressure in Group 1 Pulmonary Hypertension
Yogesh N V Reddy, Robert P Frantz, William R Miranda, et al.
Annals of the American Thoracic Society
|
July 18, 2025
Ground Glass Opacities in Pulmonary Arterial Hypertension-Results from the PVDOMICS Study
Divya Padmanabhan Menon, Robert P Frantz, Benjamin R Gochanour, et al.
Page
of 22