Statement on imaging and pulmonary hypertension from the Pulmonary Vascular Research Institute (PVRI)
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019841990
A multidisciplinary pulmonary embolism response team (PERT)—experience from a national multicenter consortium
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018824563
Treatment with low-dose tacrolimus inhibits bleeding complications in a patient with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018805406
Epidemiology and initial management of pulmonary arterial hypertension: real-world data from the Hellenic pulmOnary hyPertension rEgistry (HOPE)
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019877157
Dynamic right ventricular–pulmonary arterial uncoupling during maximum incremental exercise in exercise pulmonary hypertension and pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019862435
Hypoxia-induced pulmonary hypertension and chronic lung disease: caveolin-1 dysfunction an important underlying feature
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019837876
The efficacy and safety of pulmonary vasodilators in patients with Fontan circulation: a meta-analysis of randomized controlled trials
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018790450
Transition from parental prostacyclin to selexipag: a case series of five pulmonary arterial hypertension patients
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019862167
Adverse physiologic effects of Western diet on right ventricular structure and function: role of lipid accumulation and metabolic therapy
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018817741
SphK1/S1P mediates TGF-β1-induced proliferation of pulmonary artery smooth muscle cells and its potential mechanisms
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018816977
Clinical and hemodynamic factors in predicting response to fluid challenge during right heart catheterization
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018819803
Cardiac arrest and pulmonary hypertension in scurvy: a case report
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018812052
The use of a durable right ventricular assist device for isolated right ventricular failure due to combined pre- and postcapillary pulmonary hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019831222
Retinal vascular changes and right ventricular structure and function: the MESA-Right Ventricle and MESA-Eye studies
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018819781
Case series of seven women with uterine fibroids associated with venous thromboembolism and chronic thromboembolic disease
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018803873
Oral treprostinil in transition or as add-on therapy in pediatric pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019856471
Mortality in US veterans with pulmonary hypertension: a retrospective analysis of survival by subtype and baseline factors
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019825763
Clinical and hemodynamic benefit of macitentan and riociguat upfront combination in patients with pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019826944
Drug repositioning in pulmonary arterial hypertension: challenges and opportunities
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019832226
Elevated serum circ_0068481 levels as a potential diagnostic and prognostic indicator in idiopathic pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019888416
Enhanced circulating levels of CD3 cells-derived extracellular vesicles in different forms of pulmonary hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019864357
Severe pulmonary hypertension and reduced right ventricle systolic function associated with maternal mortality in pregnant uncorrected congenital heart diseases
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019884516
Matrix metalloproteinase 7 in diagnosis and differentiation of pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019895414
United States Pulmonary Hypertension Scientific Registry (USPHSR): rationale, design, and clinical implications
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019851696
A checkpoint on innate myeloid cells in pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018823528
Features of radiological and physiological findings in pulmonary capillary hemangiomatosis: an updated pooled analysis of confirmed diagnostic cases
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019896696
Value of lung perfusion scintigraphy in patients with idiopathic pulmonary arterial hypertension: a patchy pattern to consider
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018816968
Decreased collagen VI in the tunica media of pulmonary vessels during exposure to hypoxia: a novel step in pulmonary arterial remodeling
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019860747
Pulmonary arterial hypertension in interferonophaties: a case report and a review of the literature
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019869837
Metabolomics of exercise pulmonary hypertension are intermediate between controls and patients with pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019882623
Pulmonary endarterectomy in a 12-year-old boy with multiple comorbidities
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019886249
PPARβ/δ a potential target in pulmonary hypertension blighted by cancer risk
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018812053
Switching to riociguat: a potential treatment strategy for the management of CTEPH and PAH
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019837849
Acute vasoreactivity testing in pediatric idiopathic pulmonary arterial hypertension: an international survey on current practice
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019857533
Reduced free-living activity levels in pulmonary arterial hypertension patients
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018814182
Riociguat for the treatment of transthyretin cardiac amyloidosis: data from a named patient use program in Austria
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019849394
Imatinib for right heart failure in COPD
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018816974
Effects of oxygen therapy in a pediatric normoxemic patient with pulmonary arterial hypertension and congenital heart disease
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019845610
Rates of hospitalization associated with the use of aldosterone receptor antagonists in patients with pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019868422
Higher plasma fibroblast growth factor 23 levels are associated with a higher risk profile in pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019895446
Idiopathic hypereosinophilic syndrome with pulmonary hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018793999
Left ventricular peak early diastolic strain rate detected by two-dimensional speckle tracking echocardiography and disease severity in pre-capillary pulmonary hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019865158
“Anagrelide-induced pulmonary arterial hypertension”: a rare case of drug-induced pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019896682
Acute response to rapid iloprost inhalation using the Breelib™ nebulizer in pulmonary arterial hypertension: the Breelib™ acute study
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019875342
The prognostic value of pulmonary artery compliance in cardiogenic shock
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019877161
Myocardial bridge: an unrecognized cause of chest pain in pulmonary arterial hypertension
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019860738
Multidisciplinary pulmonary embolism care: an exciting time to join the team
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019829071
Reciprocal actions of constrictor prostanoids and superoxide in chronic hypoxia-induced pulmonary hypertension: roles of EETs
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019895947
Proximal pulmonary arterial wall disease in patients with persistent pulmonary hypertension after successful left-sided valve replacement according to the hemodynamic phenotype
来源期刊:Pulmonary CirculationDOI:10.1177/2045894018816972
Long-term study of oral treprostinil to treat pulmonary arterial hypertension: dosing, tolerability, and pharmacokinetics
来源期刊:Pulmonary CirculationDOI:10.1177/2045894019866335