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American Journal of Respiratory Cell and Molecular Biology
|
October 21, 2022
Hungry for Chloride: Reprogramming Endothelial Cell Metabolism in Pulmonary Arterial Hypertension
Simon Bousseau, Tim Lahm
Autophagy
|
May 26, 2012
LC3 as a potential therapeutic target in hypoxia-induced pulmonary hypertension
Tim Lahm, Irina Petrache
Medicine
|
August 11, 2018
A case report of hepatopulmonary syndrome in hereditary hemorrhagic telangiectasia (HHT): Not all right-to-left shunting in HHT is due to pulmonary arteriovenous malformations
Sheila Krishnan, Tim Lahm
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
June 6, 2007
Point:Counterpoint "Release of an endothelium-derived vasoconstrictor and RhoA/Rho kinase-mediated calcium sensitization of smooth muscle cell contraction are/are not the main effectors for full and sustained hypoxic pulmonary vasoconstriction"
Tim Lahm, Daniel R Meldrum
American Journal of Respiratory and Critical Care Medicine
|
September 29, 2018
The Y Chromosome Takes the Field to Modify BMPR2 Expression
Andrea L Frump, Tim Lahm
Annals of the American Thoracic Society
|
June 2, 2021
Riding the Ferrous Wheel of Iron Supplementation in Pulmonary Arterial Hypertension
Jonathan M Krasinkiewicz, Tim Lahm
Clinics in Chest Medicine
|
November 26, 2013
World Health Organization group 5 pulmonary hypertension
Tim Lahm, Murali M Chakinala
American Journal of Respiratory and Critical Care Medicine
|
June 15, 2022
Misbehaving Guests in the Right Ventricle: Macrophage-NLRP3 Activation in Pulmonary Hypertension
Rafael Sobrano Fais, Tim Lahm
The European Respiratory Journal
|
March 22, 2020
Tips for success in pulmonary hypertension treatment: progress in isolating endothelial cells from pulmonary artery catheters
Andrea L Frump, Tim Lahm
The European Respiratory Journal
|
August 5, 2017
Inhibiting oestrogen signalling in pulmonary arterial hypertension: sex, drugs and research
Tim Lahm, Steven M Kawut
Page
of 15
Search research articles
Search
Showing results (11-20 of 149) with videos related to
Sort By:
Page
of 15
American Journal of Respiratory Cell and Molecular Biology
|
October 21, 2022
Hungry for Chloride: Reprogramming Endothelial Cell Metabolism in Pulmonary Arterial Hypertension
Simon Bousseau, Tim Lahm
Autophagy
|
May 26, 2012
LC3 as a potential therapeutic target in hypoxia-induced pulmonary hypertension
Tim Lahm, Irina Petrache
Medicine
|
August 11, 2018
A case report of hepatopulmonary syndrome in hereditary hemorrhagic telangiectasia (HHT): Not all right-to-left shunting in HHT is due to pulmonary arteriovenous malformations
Sheila Krishnan, Tim Lahm
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
June 6, 2007
Point:Counterpoint "Release of an endothelium-derived vasoconstrictor and RhoA/Rho kinase-mediated calcium sensitization of smooth muscle cell contraction are/are not the main effectors for full and sustained hypoxic pulmonary vasoconstriction"
Tim Lahm, Daniel R Meldrum
American Journal of Respiratory and Critical Care Medicine
|
September 29, 2018
The Y Chromosome Takes the Field to Modify BMPR2 Expression
Andrea L Frump, Tim Lahm
Annals of the American Thoracic Society
|
June 2, 2021
Riding the Ferrous Wheel of Iron Supplementation in Pulmonary Arterial Hypertension
Jonathan M Krasinkiewicz, Tim Lahm
Clinics in Chest Medicine
|
November 26, 2013
World Health Organization group 5 pulmonary hypertension
Tim Lahm, Murali M Chakinala
American Journal of Respiratory and Critical Care Medicine
|
June 15, 2022
Misbehaving Guests in the Right Ventricle: Macrophage-NLRP3 Activation in Pulmonary Hypertension
Rafael Sobrano Fais, Tim Lahm
The European Respiratory Journal
|
March 22, 2020
Tips for success in pulmonary hypertension treatment: progress in isolating endothelial cells from pulmonary artery catheters
Andrea L Frump, Tim Lahm
The European Respiratory Journal
|
August 5, 2017
Inhibiting oestrogen signalling in pulmonary arterial hypertension: sex, drugs and research
Tim Lahm, Steven M Kawut
Page
of 15