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Pharmacotherapy in pulmonary arterial hypertension: a systematic review and meta-analysis

Respiratory research, 2010-01, Vol.11 (1), p.12-12, Article 12

2010

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Chronic Lung Allograft Dysfunction: Review of CT and Pathologic Findings

Radiology. Cardiothoracic imaging, 2021-02, Vol.3 (1), p.e200314-e200314

2021

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Riociguat: A Novel Therapeutic Option for Pulmonary Arterial Hypertension and Chronic Thromboembolic Pulmonary Hypertension

Canadian journal of cardiology, 2014-10, Vol.30 (10), p.1233-1240

2014

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Lessons from lung transplantation: Cause for redefining the pathophysiology of pulmonary hypertension in gaucher disease

Respiratory medicine case reports, 2019-01, Vol.28, p.100893, Article 100893

2019

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Clinical and hemodynamic factors in predicting response to fluid challenge during right heart catheterization

Pulmonary circulation, 2019-01, Vol.9 (1), p.1-7

2019

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Validity of algorithm for estimating left sided filling pressures on echocardiography in a population referred for pulmonary arterial hypertension

Pulmonary circulation, 2018-01, Vol.8 (1), p.1-7

2018

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Impact of targeted pulmonary arterial hypertension therapy in patients with combined post- and precapillary pulmonary hypertension

The American heart journal, 2021-05, Vol.235, p.74-81

2021

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Impact of saline loading at cardiac catheterization on the classification and management of patients evaluated for pulmonary hypertension

International journal of cardiology, 2020-05, Vol.306, p.181-186

2020

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Does community size or commute time affect severity of illness at diagnosis or quality of care in a centralized care model of pulmonary hypertension?

International journal of cardiology, 2021-06, Vol.332, p.175-181

2021

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A Clinical Classification Scheme for Tracheobronchomegaly (Mounier-Kuhn Syndrome)

Lung, 2015-10, Vol.193 (5), p.815-822

2015

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Comparison of thermodilution and indirect Fick cardiac outputs in pulmonary hypertension

International journal of cardiology, 2018-05, Vol.258, p.228-231

2018

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Assessing response to therapy in idiopathic pulmonary arterial hypertension: a consensus survey of Canadian pulmonary hypertension physicians

Canadian respiratory journal, 2011, Vol.18 (4), p.230-234

2011

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Association Between the Pulmonary Artery Pulsatility Index and Prognosis in Pulmonary Arterial Hypertension: A Multicentre Study

CJC open (Online), 2023-07, Vol.5 (7), p.545-553

2023

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IMPROVEMENT IN RIGHT ATRIAL FUNCTION IS ASSOCIATED WITH IMPROVED FUNCTIONAL CAPACITY IN PULMONARY ARTERIAL HYPERTENSION

Journal of the American College of Cardiology, 2013-03, Vol.61 (10), p.E1246-E1246

2013

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RIGHT ATRIAL EMPTYING FRACTIONS ARE ASSOCIATED WITH SURVIVAL IN PULMONARY ARTERIAL HYPERTENSION

Journal of the American College of Cardiology, 2013-03, Vol.61 (10), p.E896-E896

2013

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Prognostic utility of right atrial emptying fractions in pulmonary arterial hypertension

Pulmonary circulation, 2015-09, Vol.5 (3), p.473-480

2015

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A Limited Number of Caenorhabditis elegans Genes Are Readily Mutable to Dominant, Temperature-Sensitive Maternal-Effect Embryonic Lethality

Genetics (Austin), 1997-12, Vol.147 (4), p.1665-1674

1997

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Prognostic factors for survival in scleroderma associated pulmonary arterial hypertension

Journal of rheumatology, 2008-08, Vol.35 (8), p.1584

2008

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Improved survival of biolistically transfected mouse islet allografts expressing CTLA4-Ig or soluble Fas ligand

Transplantation, 1998-07, Vol.66 (2), p.194

1998

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Lessons from lung transplantation: Cause for redefining the pathophysiology of pulmonary hypertension in gaucher disease

Respiratory medicine case reports, 2019, Vol.28, p.100893-100893

2019

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IMPROVED SURVIVAL OF BIOLISTICALLY TRANSFECTED MOUSE ISLET ALLOGRAFTS EXPRESSING CTLA4-Ig OR SOLUBLE FAS LIGAND1

Transplantation, 1998-07, Vol.66 (2), p.194-199

1998

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Mortality trends in pulmonary arterial hypertension in Canada: a temporal analysis of survival per ESC/ERS guideline era

The European respiratory journal, 2022-06, Vol.59 (6), p.2101552

2022

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Factors that prognosticate mortality in idiopathic pulmonary arterial hypertension: A systematic review of the literature

Respiratory medicine, 2010-11, Vol.104 (11), p.1588-1607

2010

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Novel Electrodes for Underwater ECG Monitoring

IEEE transactions on biomedical engineering, 2014-06, Vol.61 (6), p.1863-1876

2014

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Pharmacotherapy in pulmonary arterial hypertension: a systematic review and meta-analysis

Chronic Lung Allograft Dysfunction: Review of CT and Pathologic Findings

Riociguat: A Novel Therapeutic Option for Pulmonary Arterial Hypertension and Chronic Thromboembolic Pulmonary Hypertension

Lessons from lung transplantation: Cause for redefining the pathophysiology of pulmonary hypertension in gaucher disease

Clinical and hemodynamic factors in predicting response to fluid challenge during right heart catheterization

Validity of algorithm for estimating left sided filling pressures on echocardiography in a population referred for pulmonary arterial hypertension

Impact of targeted pulmonary arterial hypertension therapy in patients with combined post- and precapillary pulmonary hypertension

Impact of saline loading at cardiac catheterization on the classification and management of patients evaluated for pulmonary hypertension

Does community size or commute time affect severity of illness at diagnosis or quality of care in a centralized care model of pulmonary hypertension?

A Clinical Classification Scheme for Tracheobronchomegaly (Mounier-Kuhn Syndrome)

Comparison of thermodilution and indirect Fick cardiac outputs in pulmonary hypertension

Assessing response to therapy in idiopathic pulmonary arterial hypertension: a consensus survey of Canadian pulmonary hypertension physicians

Association Between the Pulmonary Artery Pulsatility Index and Prognosis in Pulmonary Arterial Hypertension: A Multicentre Study

IMPROVEMENT IN RIGHT ATRIAL FUNCTION IS ASSOCIATED WITH IMPROVED FUNCTIONAL CAPACITY IN PULMONARY ARTERIAL HYPERTENSION

RIGHT ATRIAL EMPTYING FRACTIONS ARE ASSOCIATED WITH SURVIVAL IN PULMONARY ARTERIAL HYPERTENSION

Prognostic utility of right atrial emptying fractions in pulmonary arterial hypertension

A Limited Number of Caenorhabditis elegans Genes Are Readily Mutable to Dominant, Temperature-Sensitive Maternal-Effect Embryonic Lethality

Prognostic factors for survival in scleroderma associated pulmonary arterial hypertension

Improved survival of biolistically transfected mouse islet allografts expressing CTLA4-Ig or soluble Fas ligand

Lessons from lung transplantation: Cause for redefining the pathophysiology of pulmonary hypertension in gaucher disease

IMPROVED SURVIVAL OF BIOLISTICALLY TRANSFECTED MOUSE ISLET ALLOGRAFTS EXPRESSING CTLA4-Ig OR SOLUBLE FAS LIGAND1

Mortality trends in pulmonary arterial hypertension in Canada: a temporal analysis of survival per ESC/ERS guideline era

Factors that prognosticate mortality in idiopathic pulmonary arterial hypertension: A systematic review of the literature

Novel Electrodes for Underwater ECG Monitoring

Triaging Access to Critical Care Resources in Patients With Chronic Respiratory Diseases in the Event of a Major COVID-19 Surge: Key Highlights From the Canadian Thoracic Society (CTS) Position Statement

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