Works matching IS 20458932 AND DT 2019 AND VI 9 AND IP 3
Results: 29
Diminished right ventricular function at diagnosis of pulmonary hypertension is associated with mortality in bronchopulmonary dysplasia.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019878598
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- Article
Epidemiology and initial management of pulmonary arterial hypertension: real‐world data from the Hellenic pulmOnary hyPertension rEgistry (HOPE)
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019877157
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- Article
Iptakalim ameliorates hypoxia‐impaired human endothelial colony‐forming cells proliferation, migration, and angiogenesis via Akt/eNOS pathways.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019875417
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Mutually reinforcing effects of genetic variants and interferon‐β 1a therapy for pulmonary arterial hypertension development in multiple sclerosis patients.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019872192
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- Article
The prognostic value of pulmonary artery compliance in cardiogenic shock.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019877161
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- Article
Inactivation of carboxyl terminus of Hsc70-interacting protein prevents hypoxia-induced pulmonary arterial smooth muscle cells proliferation by reducing intracellular Ca<sup>2+</sup> concentration.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019875343
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- Article
Acute response to rapid iloprost inhalation using the Breelib™ nebulizer in pulmonary arterial hypertension: the Breelib™ acute study.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019875342
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Pulmonary arterial hypertension in interferonophaties: a case report and a review of the literature.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019869837
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Cardiac sympathetic dysfunction in pulmonary arterial hypertension: lesson from left-sided heart failure.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019868620
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Rates of hospitalization associated with the use of aldosterone receptor antagonists in patients with pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019868422
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- Article
Angiogenic profile identifies pulmonary hypertension in children with Down syndrome.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019866549
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Pulmonary hypertension with dasatinib and other tyrosine kinase inhibitors.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019865704
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Products of oxidative stress and transient receptor potential ankyrin A1 expression in the brainstem after lung ischemia-reperfusion injury.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019865169
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- Article
Left ventricular peak early diastolic strain rate detected by two-dimensional speckle tracking echocardiography and disease severity in pre-capillary pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019865158
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- Article
Enhanced circulating levels of CD3 cells-derived extracellular vesicles in different forms of pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019864357
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Dynamic right ventricular-pulmonary arterial uncoupling during maximum incremental exercise in exercise pulmonary hypertension and pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019862435
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Transition from parental prostacyclin to selexipag: a case series of five pulmonary arterial hypertension patients.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019862167
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Oral treprostinil use in children: a multicenter, observational experience.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019862138
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Decreased collagen VI in the tunica media of pulmonary vessels during exposure to hypoxia: a novel step in pulmonary arterial remodeling.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019860747
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The expression of survivin in irreversible pulmonary arterial hypertension rats and its value in evaluating the reversibility of pulmonary arterial hypertension secondary to congenital heart disease.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019859480
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Serum uric acid as a marker of disease risk, severity, and survival in systemic sclerosis-related pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019859477
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Oral treprostinil in transition or as add-on therapy in pediatric pulmonary arterial hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019856471
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Right heart in pulmonary hypertension: from adaptation to failure.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019845611
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Statement on imaging and pulmonary hypertension from the Pulmonary Vascular Research Institute (PVRI).
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019841990
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Parameters associated with outcome in pediatric patients with congenital heart disease and pulmonary hypertension subjected to combined vasodilator and surgical treatments.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019837885
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Sildenafil for bronchopulmonary dysplasia and pulmonary hypertension: a meta-analysis.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019837875
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Advanced interstitial lung fibrosis with emphysema and pulmonary hypertension with no evidence for interstitial lung disease on high resolution CT.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894019832214
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A multidisciplinary pulmonary embolism response team (PERT)--experience from a national multicenter consortium.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894018824563
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Assessment of quality of life in pediatric patients with pulmonary hypertension.
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- Pulmonary Circulation, 2019, v. 9, n. 3, p. 1, doi. 10.1177/2045894018822985
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- Article