Works matching IS 20458932 AND DT 2019 AND VI 9 AND IP 4
Results: 30
Features of radiological and physiological findings in pulmonary capillary hemangiomatosis: an updated pooled analysis of confirmed diagnostic cases.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019896696
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‘‘Anagrelide-induced pulmonary arterial hypertension’’: a rare case of drug-induced pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019896682
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Liver transplantation in a patient with hereditary haemorrhagic telangiectasia and pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019896677
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Reciprocal actions of constrictor prostanoids and superoxide in chronic hypoxia-induced pulmonary hypertension: roles of EETs.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019895947
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Natriuretic peptide receptor C contributes to disproportionate right ventricular hypertrophy in a rodent model of obesity-induced heart failure with preserved ejection fraction with pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019895452
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Anticoagulation in pulmonary arterial hypertension: a decision analysis.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019895451
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Higher plasma fibroblast growth factor 23 levels are associated with a higher risk profile in pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019895446
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Echocardiographic estimation of right ventricular wall tension: haemodynamic comparison and long-term follow-up.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019895420
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Matrix metalloproteinase 7 in diagnosis and differentiation of pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019895414
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The prognostic value of DLCO and pulmonary blood flow in patients with pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019894531
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Comparison of the capability of risk stratification evaluation between two- and three-dimensional speckle-tracking strain in pre-capillary pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019894525
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Utilising artificial intelligence to determine patients at risk of a rare disease: idiopathic pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019890549
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Hot topics in the mechanisms of pulmonary arterial hypertension disease: cancer-like pathobiology, the role of the adventitia, systemic involvement, and right ventricular failure.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019889775
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Prediction value of pulmonary hypertension in newly identified left ventricular dysfunction among adult patients after patent ductus arteriosus closure.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019888428
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Elevated serum circ_0068481 levels as a potential diagnostic and prognostic indicator in idiopathic pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019888416
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Pulmonary endarterectomy in a 12-year-old boy with multiple comorbidities.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019886249
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Exploring a physiotherapy well-being review to deliver community-based rehabilitation in patients with pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019885356
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Severe pulmonary hypertension and reduced right ventricle systolic function associated with maternal mortality in pregnant uncorrected congenital heart diseases.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019884516
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Optimizing imaging of the rat pulmonary microvasculature by micro-computed tomography.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019883613
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Impact of right ventricular dyssynchrony on prognosis of patients with idiopathic pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019883609
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Cytokines trigger disruption of endothelium barrier function and p38 MAP kinase activation in BMPR2-silenced human lung microvascular endothelial cells.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019883607
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Clinical outcomes of inferior vena cava filter in complicated pulmonary embolism.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019882636
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Congenital heart disease, pulmonary arterial hypertension and the UK’s Drivers and Vehicle Licensing Agency: controversial new guidance.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019882627
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Metabolomics of exercise pulmonary hypertension are intermediate between controls and patients with pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019882623
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Orotracheal treprostinil administration attenuates bleomycin-induced lung injury, vascular remodeling, and fibrosis in mice.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019881954
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Long non-coding RNA expression profiling in the lungs of pulmonary arterial hypertension rats with acute inflammation.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019879393
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Long-term results of the DelIVery for Pulmonary Arterial Hypertension trial.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019878615
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Acute vasoreactivity testing in pediatric idiopathic pulmonary arterial hypertension: an international survey on current practice.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019857533
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Baicalin prevents pulmonary arterial remodeling in vivo via the AKT/ERK/NF-κB signaling pathways.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019878599
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Riociguat for the treatment of transthyretin cardiac amyloidosis: data from a named patient use program in Austria.
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- Pulmonary Circulation, 2019, v. 9, n. 4, p. 1, doi. 10.1177/2045894019849394
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