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Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertension

Circulation (New York, N.Y.), 2010-08, Vol.122 (9), p.920-927

2010

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Dynamic changes in lung microRNA profiles during the development of pulmonary hypertension due to chronic hypoxia and monocrotaline

Arteriosclerosis, thrombosis, and vascular biology, 2010-04, Vol.30 (4), p.716-723

2010

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Long-term Use of Sildenafil in Inoperable Chronic Thromboembolic Pulmonary Hypertension

Chest, 2008-08, Vol.134 (2), p.229-236

2008

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Decreased time constant of the pulmonary circulation in chronic thromboembolic pulmonary hypertension

American journal of physiology. Heart and circulatory physiology, 2013-07, Vol.305 (2), p.H259-H264

2013

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Evidence of Dysfunction of Endothelial Progenitors in Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2009-10, Vol.180 (8), p.780-787

2009

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Impaired Natural Killer Cell Phenotype and Function in Idiopathic and Heritable Pulmonary Arterial Hypertension

Circulation (New York, N.Y.), 2012-08, Vol.126 (9), p.1099-1109

2012

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Occlusion pressure analysis role in partitioning of pulmonary vascular resistance in CTEPH

The European respiratory journal, 2012-09, Vol.40 (3), p.612-617

2012

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A New Way to See a Bronchopleural Fistula

American journal of respiratory and critical care medicine, 2016-07, Vol.194 (2), p.239-240

2016

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Risk of Potentially Life-Threatening Thyroid Dysfunction Due to Amiodarone in Idiopathic Pulmonary Arterial Hypertension Patients

Journal of the American College of Cardiology, 2011-02, Vol.57 (8), p.997-998

2011

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Pulmonary arterial size and response to sildenafil in chronic thromboembolic pulmonary hypertension

The Journal of heart and lung transplantation, 2010-06, Vol.29 (6), p.610-615

2010

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Bone morphogenetic protein receptor type II deficiency and increased inflammatory cytokine production. A gateway to pulmonary arterial hypertension

American journal of respiratory and critical care medicine, 2015-10, Vol.192 (7), p.859-872

2015

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Stomach versus lungs: the case of a giant hiatal hernia

Thorax, 2015-02, Vol.70 (2), p.200-201

2015

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Stomach versus lungs: the case of a giant hiatal hernia: Figure 1

Thorax, 2015-02, Vol.70 (2), p.200-201

2015

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Different Cytokine Patterns in BMPR2-Mutation-Positive Patients and Patients With Pulmonary Arterial Hypertension Without Mutations and Their Influence on Survival

Chest, 2022-06, Vol.161 (6), p.1651-1656

2022

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Levetiracetam-induced eosinophilic pneumonia

BMJ case reports, 2017-03, Vol.2017, p.bcr2016219121

2017

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Better off Blue: BMPR-2 Mutation, Arteriovenous Malformation, and Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2014-06, Vol.189 (11), p.1435-1436

2014

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Unexplained iron deficiency in idiopathic and heritable pulmonary arterial hypertension

Thorax, 2011-04, Vol.66 (4), p.326-332

2011

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Hepatic Shunting of Eggs and Pulmonary Vascular Remodeling in Bmpr2(+/-) Mice with Schistosomiasis

American journal of respiratory and critical care medicine, 2015-12, Vol.192 (11), p.1355-1365

2015

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Praziquantel Reverses Pulmonary Hypertension and Vascular Remodeling in Murine Schistosomiasis

American journal of respiratory and critical care medicine, 2011-08, Vol.184 (4), p.467-473

2011

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18FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study

Pulmonary circulation, 2011-10, Vol.1 (4), p.448-455

2011

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BMPR-II mutations promote pulmonary arterial hypertension via a hyperinflammatory response

Clinical medicine (London, England), 2015-06, Vol.15 (3), p.s15-s15

2015

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Reply to "Letter to the editor: 'Pulsatile pulmonary artery pressure: are fluid-filled catheters accurate in pulmonary hypertension?'"

American journal of physiology. Heart and circulatory physiology, 2013-12, Vol.305 (11), p.H1682-H1682

2013

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Hepatic Shunting of Eggs and Pulmonary Vascular Remodeling in Bmpr2^sup +/-^ Mice with Schistosomiasis

American journal of respiratory and critical care medicine, 2015-12, Vol.192 (11), p.1355

2015

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Risk of Potentially Life-Threatening Thyroid Dysfunction Due to Amiodarone in Idiopathic Pulmonary Arterial Hypertension Patients: Research Correspondence

Journal of the American College of Cardiology, 2011-02, Vol.57 (8), p.997-998

2011

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Hematopoietic stem cell transplantation alters susceptibility to pulmonary hypertension in Bmpr2-deficient mice

Pulmonary circulation, 2018-10, Vol.8 (4), p.1-9

2018

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Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertension

Dynamic changes in lung microRNA profiles during the development of pulmonary hypertension due to chronic hypoxia and monocrotaline

Long-term Use of Sildenafil in Inoperable Chronic Thromboembolic Pulmonary Hypertension

Decreased time constant of the pulmonary circulation in chronic thromboembolic pulmonary hypertension

Evidence of Dysfunction of Endothelial Progenitors in Pulmonary Arterial Hypertension

Impaired Natural Killer Cell Phenotype and Function in Idiopathic and Heritable Pulmonary Arterial Hypertension

Occlusion pressure analysis role in partitioning of pulmonary vascular resistance in CTEPH

A New Way to See a Bronchopleural Fistula

Risk of Potentially Life-Threatening Thyroid Dysfunction Due to Amiodarone in Idiopathic Pulmonary Arterial Hypertension Patients

Pulmonary arterial size and response to sildenafil in chronic thromboembolic pulmonary hypertension

Bone morphogenetic protein receptor type II deficiency and increased inflammatory cytokine production. A gateway to pulmonary arterial hypertension

Stomach versus lungs: the case of a giant hiatal hernia

Stomach versus lungs: the case of a giant hiatal hernia: Figure 1

Different Cytokine Patterns in BMPR2-Mutation-Positive Patients and Patients With Pulmonary Arterial Hypertension Without Mutations and Their Influence on Survival

Levetiracetam-induced eosinophilic pneumonia

Better off Blue: BMPR-2 Mutation, Arteriovenous Malformation, and Pulmonary Arterial Hypertension

Unexplained iron deficiency in idiopathic and heritable pulmonary arterial hypertension

Hepatic Shunting of Eggs and Pulmonary Vascular Remodeling in Bmpr2(+/-) Mice with Schistosomiasis

Praziquantel Reverses Pulmonary Hypertension and Vascular Remodeling in Murine Schistosomiasis

18FDG PET imaging can quantify increased cellular metabolism in pulmonary arterial hypertension: A proof-of-principle study

BMPR-II mutations promote pulmonary arterial hypertension via a hyperinflammatory response

Reply to "Letter to the editor: 'Pulsatile pulmonary artery pressure: are fluid-filled catheters accurate in pulmonary hypertension?'"

Hepatic Shunting of Eggs and Pulmonary Vascular Remodeling in Bmpr2^sup +/-^ Mice with Schistosomiasis

Risk of Potentially Life-Threatening Thyroid Dysfunction Due to Amiodarone in Idiopathic Pulmonary Arterial Hypertension Patients: Research Correspondence

Hematopoietic stem cell transplantation alters susceptibility to pulmonary hypertension in Bmpr2-deficient mice

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