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High-sensitivity C-reactive protein in heart failure with preserved ejection fraction

PloS one, 2018-08, Vol.13 (8), p.e0201836-e0201836

2018

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Pulmonary vascular disease in pulmonary hypertension due to left heart disease: pathophysiologic implications

European heart journal, 2022-09, Vol.43 (36), p.3417-3431

2022

Volltextzugriff (PDF)

Intravenous Bevacizumab for Refractory Hereditary Hemorrhagic Telangiectasia–Related Epistaxis and Gastrointestinal Bleeding

Mayo Clinic proceedings, 2018-02, Vol.93 (2), p.155-166

2018

Volltextzugriff (PDF)

Pulmonary hypertension patient perspectives toward pulmonary rehabilitation

Pulmonary circulation, 2024-01, Vol.14 (1), p.e12338-n/a

2024

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Portopulmonary Hypertension: Management and Liver Transplantation Evaluation

Chest, 2023-07, Vol.164 (1), p.206-214

DuBrock, Hilary M

2023

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Cardiac index and hepatopulmonary syndrome in liver transplantation candidates: The pulmonary vascular complications of liver disease study

Liver transplantation, 2023-05, Vol.29 (5), p.467-475

2023

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Topic-Based, Recent Literature Review on Pulmonary Hypertension

Mayo Clinic proceedings, 2021-12, Vol.96 (12), p.3109-3121

2021

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Predictors of Waitlist Mortality in Portopulmonary Hypertension

Transplantation, 2017-07, Vol.101 (7), p.1609

2017

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Development of the Pulmonary Hypertension Functional Classification Self-Report: a patient version adapted from the World Health Organization Functional Classification measure

Health and quality of life outcomes, 2021-08, Vol.19 (1), p.1-202, Article 202

2021

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CAQ Corner: Cardiovascular and pulmonary evaluation of liver transplantation candidates: What you need to know for the board exam

Liver transplantation, 2022-09, Vol.28 (9), p.1529-1538

2022

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Pulmonary hypertension due to interstitial lung disease or chronic obstructive pulmonary disease: a patient experience study of symptoms and their impact on quality of life

Pulmonary circulation, 2021-04, Vol.11 (2), p.1-9

2021

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Global Pulmonary Vascular Remodeling in Pulmonary Hypertension Associated With Heart Failure and Preserved or Reduced Ejection Fraction

Circulation (New York, N.Y.), 2018-04, Vol.137 (17), p.1796-1810

2018

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Inhaled treprostinil in patients with pulmonary hypertension associated with interstitial lung disease with less severe haemodynamics: a post hoc analysis of the INCREASE study

BMJ open respiratory research, 2024-03, Vol.11 (1), p.e002116

2024

Volltextzugriff (PDF)

Temporal Trends in Portopulmonary Hypertension Model for End-stage Liver Disease Exceptions and Outcomes

Transplantation direct, 2022-12, Vol.8 (12), p.e1410-e1410

2022

Volltextzugriff (PDF)

The Myths and Realities of Portopulmonary Hypertension

Hepatology (Baltimore, Md.), 2020-10, Vol.72 (4), p.1455-1460

2020

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Bezold–Jarisch reflex mediated syncope in pulmonary arterial hypertension: An illustrative case series

Pulmonary circulation, 2022-10, Vol.12 (4), p.e12147-e12147

2022

Volltextzugriff (PDF)

Using PAH‐SYMPACT to assess quality of life in patients with pulmonary hypertension associated with chronic lung disease

Pulmonary circulation, 2024-01, Vol.14 (1), p.e12343-n/a

2024

Volltextzugriff (PDF)

Outcomes of Liver Transplantation in Treated Portopulmonary Hypertension Patients With a Mean Pulmonary Arterial Pressure ≥35 mm Hg

Transplantation direct, 2020-12, Vol.6 (12), p.e630-e630

2020

Volltextzugriff (PDF)

Do Late Bubbles Correspond to Early Hepatopulmonary Syndrome?

Annals of hepatology, 2017-07, Vol.16 (4), p.476-477

2017

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The feasibility and value of assessing patient‐reported outcomes in pulmonary arterial hypertension

Pulmonary circulation, 2022-10, Vol.12 (4), p.e12143-n/a

2022

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Bubble Trouble in COVID-19

American journal of respiratory and critical care medicine, 2020-10, Vol.202 (7), p.926-928

2020

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Portopulmonary Hypertension: A Survey of Practice Patterns and Provider Attitudes

Transplantation direct, 2019-06, Vol.5 (6), p.e456-e456

2019

Volltextzugriff (PDF)

Mending the Model for End‐Stage Liver Disease: An in‐depth review of the past, present, and future portopulmonary hypertension Model for End‐Stage Liver Disease exception

Liver transplantation, 2022-07, Vol.28 (7), p.1224-1230

2022

Volltextzugriff (PDF)

Sex Differences in Portopulmonary Hypertension

Chest, 2021-01, Vol.159 (1), p.328-336

2021

Volltextzugriff (PDF)

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High-sensitivity C-reactive protein in heart failure with preserved ejection fraction

Pulmonary vascular disease in pulmonary hypertension due to left heart disease: pathophysiologic implications

Intravenous Bevacizumab for Refractory Hereditary Hemorrhagic Telangiectasia–Related Epistaxis and Gastrointestinal Bleeding

Pulmonary hypertension patient perspectives toward pulmonary rehabilitation

Portopulmonary Hypertension: Management and Liver Transplantation Evaluation

Cardiac index and hepatopulmonary syndrome in liver transplantation candidates: The pulmonary vascular complications of liver disease study

Topic-Based, Recent Literature Review on Pulmonary Hypertension

Predictors of Waitlist Mortality in Portopulmonary Hypertension

Development of the Pulmonary Hypertension Functional Classification Self-Report: a patient version adapted from the World Health Organization Functional Classification measure

CAQ Corner: Cardiovascular and pulmonary evaluation of liver transplantation candidates: What you need to know for the board exam

Pulmonary hypertension due to interstitial lung disease or chronic obstructive pulmonary disease: a patient experience study of symptoms and their impact on quality of life

Health disparities and treatment approaches in portopulmonary hypertension and idiopathic pulmonary arterial hypertension: an analysis of the Pulmonary Hypertension Association Registry

Global Pulmonary Vascular Remodeling in Pulmonary Hypertension Associated With Heart Failure and Preserved or Reduced Ejection Fraction

Inhaled treprostinil in patients with pulmonary hypertension associated with interstitial lung disease with less severe haemodynamics: a post hoc analysis of the INCREASE study

Temporal Trends in Portopulmonary Hypertension Model for End-stage Liver Disease Exceptions and Outcomes

The Myths and Realities of Portopulmonary Hypertension

Bezold–Jarisch reflex mediated syncope in pulmonary arterial hypertension: An illustrative case series

Using PAH‐SYMPACT to assess quality of life in patients with pulmonary hypertension associated with chronic lung disease

Outcomes of Liver Transplantation in Treated Portopulmonary Hypertension Patients With a Mean Pulmonary Arterial Pressure ≥35 mm Hg

Do Late Bubbles Correspond to Early Hepatopulmonary Syndrome?

The feasibility and value of assessing patient‐reported outcomes in pulmonary arterial hypertension

Bubble Trouble in COVID-19

Portopulmonary Hypertension: A Survey of Practice Patterns and Provider Attitudes

Mending the Model for End‐Stage Liver Disease: An in‐depth review of the past, present, and future portopulmonary hypertension Model for End‐Stage Liver Disease exception

Sex Differences in Portopulmonary Hypertension

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