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P Frantz

Showing results (141-150 of 247) with videos related to

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Pharmacogenetics and Genomics|October 15, 2013
TPMT genetic variants are associated with increased rejection with azathioprine use in heart transplantationJackson J Liang, Jennifer R Geske, Barry A Boilson, et al.
Journal of Cardiothoracic and Vascular Anesthesia|December 4, 2019
Outcomes After Noncardiac Surgery for Patients with Pulmonary Hypertension: A Historical Cohort StudyAtousa Deljou, Moldovan Sabov, Garvan C Kane, et al.
Chest|December 28, 2020
Impact of Right Ventricular Dysfunction on Short-term and Long-term Mortality in Sepsis: A Meta-analysis of 1,373 PatientsSaraschandra Vallabhajosyula, Aditi Shankar, Rahul Vojjini, et al.
Chest|January 23, 2018
Baseline and Serial Brain Natriuretic Peptide Level Predicts 5-Year Overall Survival in Patients With Pulmonary Arterial Hypertension: Data From the REVEAL RegistryRobert P Frantz, Harrison W Farber, David B Badesch, et al.
Chest|November 10, 2018
ResponseRobert P Frantz, Carol Zhao, Harrison W Farber, et al.
Pulmonary Circulation|February 12, 2024
Hemodynamic response to inhaled nitric oxide in patients with pulmonary hypertension and chronic kidney disease: A retrospective cohort studyKathryn T Del Valle, Michael J Krowka, Carrie A Schinstock, et al.
BMJ (Clinical Research Ed.)|April 14, 2016
Re-evaluation of the traditional diet-heart hypothesis: analysis of recovered data from Minnesota Coronary Experiment (1968-73)Christopher E Ramsden, Daisy Zamora, Sharon Majchrzak-Hong, et al.
The Lancet. Respiratory Medicine|August 23, 2021
Selonsertib in adults with pulmonary arterial hypertension (ARROW): a randomised, double-blind, placebo-controlled, phase 2 trialStephan Rosenkranz, Jeremy Feldman, Vallerie V McLaughlin, et al.
Pulmonary Circulation|July 22, 2021
Mate-pair sequencing identifies a cryptic <i>BMPR2</i> mutation in hereditary pulmonary arterial hypertensionSarah J Chalmers, Stephen J Murphy, Laura L Thompson, et al.
Circulation|November 21, 2007
Conversion to sirolimus as primary immunosuppression attenuates the progression of allograft vasculopathy after cardiac transplantationEugenia Raichlin, Jang-Ho Bae, Zain Khalpey, et al.
Pageof 25

Showing results (141-150 of 247) with videos related to

Sort By:
Pageof 25
Pharmacogenetics and Genomics|October 15, 2013
TPMT genetic variants are associated with increased rejection with azathioprine use in heart transplantationJackson J Liang, Jennifer R Geske, Barry A Boilson, et al.
Journal of Cardiothoracic and Vascular Anesthesia|December 4, 2019
Outcomes After Noncardiac Surgery for Patients with Pulmonary Hypertension: A Historical Cohort StudyAtousa Deljou, Moldovan Sabov, Garvan C Kane, et al.
Chest|December 28, 2020
Impact of Right Ventricular Dysfunction on Short-term and Long-term Mortality in Sepsis: A Meta-analysis of 1,373 PatientsSaraschandra Vallabhajosyula, Aditi Shankar, Rahul Vojjini, et al.
Chest|January 23, 2018
Baseline and Serial Brain Natriuretic Peptide Level Predicts 5-Year Overall Survival in Patients With Pulmonary Arterial Hypertension: Data From the REVEAL RegistryRobert P Frantz, Harrison W Farber, David B Badesch, et al.
Chest|November 10, 2018
ResponseRobert P Frantz, Carol Zhao, Harrison W Farber, et al.
Pulmonary Circulation|February 12, 2024
Hemodynamic response to inhaled nitric oxide in patients with pulmonary hypertension and chronic kidney disease: A retrospective cohort studyKathryn T Del Valle, Michael J Krowka, Carrie A Schinstock, et al.
BMJ (Clinical Research Ed.)|April 14, 2016
Re-evaluation of the traditional diet-heart hypothesis: analysis of recovered data from Minnesota Coronary Experiment (1968-73)Christopher E Ramsden, Daisy Zamora, Sharon Majchrzak-Hong, et al.
The Lancet. Respiratory Medicine|August 23, 2021
Selonsertib in adults with pulmonary arterial hypertension (ARROW): a randomised, double-blind, placebo-controlled, phase 2 trialStephan Rosenkranz, Jeremy Feldman, Vallerie V McLaughlin, et al.
Pulmonary Circulation|July 22, 2021
Mate-pair sequencing identifies a cryptic <i>BMPR2</i> mutation in hereditary pulmonary arterial hypertensionSarah J Chalmers, Stephen J Murphy, Laura L Thompson, et al.
Circulation|November 21, 2007
Conversion to sirolimus as primary immunosuppression attenuates the progression of allograft vasculopathy after cardiac transplantationEugenia Raichlin, Jang-Ho Bae, Zain Khalpey, et al.
Pageof 25