BACKGROUND: Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertension (IPAH). However, hemostatic abnormalities in this disease remain poorly understood. Therefore, we aimed to study markers of thrombogenesis and fibrinolysis in patients with IPAH. METHODS: We studied 27 consecutive patients (67% female) with IPAH aged 50.0 years (IQR: 41.0-65.0) and 16 controls without pulmonary hypertension. Prothrombin fragment 1+2 (F1+2) and thrombin-antithrombin (TAT) complexes were measured to assess thrombogenesis; tissue-type plasminogen activator (tPA) antigen and plasmin-anti-plasmin complex to characterize activation of fibrinolysis; plasminogen activator inhibitor 1 (PAI-1) to measure inhibition of fibrinolysis;...
Introduction Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic interstitial l...
Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic interstitial lung disease w...
Pulmonary hypertension (PH) is a rare but disabling disorder, characterised by raised pulmonary arte...
Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertension (IPAH). ...
Abstract Background The severity of pulmonary arterial hypertension (PAH) is classified based on mea...
<p>There is a complex and not fully elucidated association between pulmonary arterial hypertension (...
SummaryBackgroundThe pathogenesis of idiopathic pulmonary arterial hypertension (IPAH) is unknown, a...
Pathogenesis of idiopathic pulmonary arterial hypertension (iPAH) includes endothelial dysfunction a...
Many pathophysiologic processes of pulmonary arterial hypertension (PAH), namely, excess vasoconstri...
Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease associated with significant morbid...
RATIONALE: Autoimmunity is thought to play a role in idiopathic pulmonary arterial hypertension (IPA...
Pulmonary hypertension (PH) is an affection with an endothelial dysfunction and in situ thromboses. ...
Background: Inflammation is known to be a feature of pulmonary arterial hypertension (PAH) and incre...
Aim: The aim of the present study was to identify the possible genotypic association of 3\u2032UTR H...
<div><p>Introduction</p><p>Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic ...
Introduction Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic interstitial l...
Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic interstitial lung disease w...
Pulmonary hypertension (PH) is a rare but disabling disorder, characterised by raised pulmonary arte...
Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertension (IPAH). ...
Abstract Background The severity of pulmonary arterial hypertension (PAH) is classified based on mea...
<p>There is a complex and not fully elucidated association between pulmonary arterial hypertension (...
SummaryBackgroundThe pathogenesis of idiopathic pulmonary arterial hypertension (IPAH) is unknown, a...
Pathogenesis of idiopathic pulmonary arterial hypertension (iPAH) includes endothelial dysfunction a...
Many pathophysiologic processes of pulmonary arterial hypertension (PAH), namely, excess vasoconstri...
Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease associated with significant morbid...
RATIONALE: Autoimmunity is thought to play a role in idiopathic pulmonary arterial hypertension (IPA...
Pulmonary hypertension (PH) is an affection with an endothelial dysfunction and in situ thromboses. ...
Background: Inflammation is known to be a feature of pulmonary arterial hypertension (PAH) and incre...
Aim: The aim of the present study was to identify the possible genotypic association of 3\u2032UTR H...
<div><p>Introduction</p><p>Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic ...
Introduction Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic interstitial l...
Idiopathic Pulmonary Fibrosis (IPF) is a progressive, incurable fibrotic interstitial lung disease w...
Pulmonary hypertension (PH) is a rare but disabling disorder, characterised by raised pulmonary arte...