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Sitaxentan-induced hepatic failure in two patients with pulmonary arterial hypertension

The European respiratory journal, 2009-09, Vol.34 (3), p.770-771

2009

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Primary pulmonary hypertension

The Lancet (British edition), 1998-08, Vol.352 (9129), p.719-725

1998

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Dysfunctional voltage-gated K+ channels in pulmonary artery smooth muscle cells of patients with primary pulmonary hypertension

Circulation (New York, N.Y.), 1998-10, Vol.98 (14), p.1400-1406

1998

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Continuous intravenous epoprostenol for pulmonary hypertension due to the scleroderma spectrum of disease. A randomized, controlled trial

Annals of internal medicine, 2000-03, Vol.132 (6), p.425

2000

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Heme Oxygenase 2: Endothelial and Neuronal Localization and Role in Endothelium-Dependent Relaxation

Proceedings of the National Academy of Sciences - PNAS, 1996-01, Vol.93 (2), p.795-798

1996

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Sitaxsentan: an endothelin-A receptor antagonist for the treatment of pulmonary arterial hypertension

International journal of clinical practice (Esher), 2006-04, Vol.60 (4), p.475-481

2006

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Epoprostenol for Treatment of Pulmonary Hypertension in Patients With Systemic Lupus Erythematosus

Chest, 2000-01, Vol.117 (1), p.14-18

2000

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The influence of continuous intravenous prostacyclin therapy for primary pulmonary hypertension on the timing and outcome of transplantation

The Journal of heart and lung transplantation, 1998-07, Vol.17 (7), p.679

1998

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Pulmonary arterial hypertension and the state of limbo

European respiratory review, 2010-12, Vol.19 (118), p.264-265

2010

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Action of fenfluramine on voltage- gated K+ channels in human pulmonary-artery smooth-muscle cells

The Lancet (British edition), 1998-07, Vol.352 (9124), p.290-290

1998

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Case 2: Silicosis

Irish medical journal, 2013-06, Vol.106 (6), p.181-182

2013

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Continuous Intravenous Epoprostenol Therapy for Pulmonary Hypertension in Gaucher's Disease

Chest, 1999-10, Vol.116 (4), p.1127-1129

1999

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Case 1: chronic thromboembolic pulmonary hypertension (CTEPH)

Irish medical journal, 2013-05, Vol.106 (5), p.146-147

2013

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Confidence from experience: dual endothelin receptor antagonism in PAH

European respiratory review, 2007-08, Vol.16 (102), p.1-2

2007

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Anastomotic pulmonary hypertension after lung transplantation for primary pulmonary hypertension : Report of surgical correction

Chest, 1999-08, Vol.116 (2), p.564-566

1999

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Lung Transplantation for Pulmonary Hypertension

Seminars in respiratory and critical care medicine, 2001-10, Vol.22 (5), p.533-540

2001

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Pulmonary Alveolar Proteinosis: Lung Transplant or Bone Marrow Transplant?

Chest, 1998-02, Vol.113 (2), p.563-564

1998

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Attenuated K + channel gene transcription in primary pulmonary hypertension

The Lancet (British edition), 1998-03, Vol.351 (9104), p.726-727

1998

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Liver transplantation in patients with severe portopulmonary hypertension treated with preoperative chronic intravenous epoprostenol

Liver transplantation, 2001-08, Vol.7 (8), p.745-749

2001

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α1L-Adrenoceptors in Canine Pulmonary Artery

Journal of cardiovascular pharmacology, 1998-08, Vol.32 (2), p.308-316

1998

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Recreational Use of Aminorex and Pulmonary Hypertension

Chest, 2000-11, Vol.118 (5), p.1496-1497

2000

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Lung transplantation and systemic sclerosis

Annals of transplantation, 2000, Vol.5 (3), p.38-43

2000

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Primary Pulmonary Hypertension Is Not Associated With Scleroderma-Like Changes in Nailfold Capillaries

Chest, 2001-09, Vol.120 (3), p.796-800

2001

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Hypoxic pulmonary endothelial cells release a diffusible contractile factor distinct from endothelin

American journal of physiology. Lung cellular and molecular physiology, 1998-04, Vol.274 (4), p.657-L664

1998

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D19 CLINICAL STUDIES IN PH: Targeting The Prostacyclin Pathway In The Treatment Of Connective Tissue Disease Associated Pulmonary Arterial Hypertension (pah): Insights From The Randomized Controlled Griphon Trial With Selexipag

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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Sitaxentan-induced hepatic failure in two patients with pulmonary arterial hypertension

Primary pulmonary hypertension

Dysfunctional voltage-gated K+ channels in pulmonary artery smooth muscle cells of patients with primary pulmonary hypertension

Continuous intravenous epoprostenol for pulmonary hypertension due to the scleroderma spectrum of disease. A randomized, controlled trial

Heme Oxygenase 2: Endothelial and Neuronal Localization and Role in Endothelium-Dependent Relaxation

Sitaxsentan: an endothelin-A receptor antagonist for the treatment of pulmonary arterial hypertension

Epoprostenol for Treatment of Pulmonary Hypertension in Patients With Systemic Lupus Erythematosus

The influence of continuous intravenous prostacyclin therapy for primary pulmonary hypertension on the timing and outcome of transplantation

Pulmonary arterial hypertension and the state of limbo

Action of fenfluramine on voltage- gated K+ channels in human pulmonary-artery smooth-muscle cells

Case 2: Silicosis

Continuous Intravenous Epoprostenol Therapy for Pulmonary Hypertension in Gaucher's Disease

Case 1: chronic thromboembolic pulmonary hypertension (CTEPH)

Confidence from experience: dual endothelin receptor antagonism in PAH

Anastomotic pulmonary hypertension after lung transplantation for primary pulmonary hypertension : Report of surgical correction

Lung Transplantation for Pulmonary Hypertension

Pulmonary Alveolar Proteinosis: Lung Transplant or Bone Marrow Transplant?

Attenuated K + channel gene transcription in primary pulmonary hypertension

Liver transplantation in patients with severe portopulmonary hypertension treated with preoperative chronic intravenous epoprostenol

α1L-Adrenoceptors in Canine Pulmonary Artery

Recreational Use of Aminorex and Pulmonary Hypertension

Lung transplantation and systemic sclerosis

Primary Pulmonary Hypertension Is Not Associated With Scleroderma-Like Changes in Nailfold Capillaries

Hypoxic pulmonary endothelial cells release a diffusible contractile factor distinct from endothelin

D19 CLINICAL STUDIES IN PH: Targeting The Prostacyclin Pathway In The Treatment Of Connective Tissue Disease Associated Pulmonary Arterial Hypertension (pah): Insights From The Randomized Controlled Griphon Trial With Selexipag

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