Mario Mezzapesa
Overview
Explore the profile of Mario Mezzapesa including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
8
Citations
136
Followers
0
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Recent Articles
1.
Mascia L, Fanelli V, Mistretta A, Filippini M, Zanin M, Berardino M, et al.
Am J Respir Crit Care Med
. 2024 Sep;
210(9):1123-1131.
PMID: 39288368
Lung-protective strategies using low Vt and moderate positive end-expiratory pressure (PEEP) are considered best practice in critical care, but interventional trials have never been conducted in patients with acute brain...
2.
Zacchetti L, Brivio M, Mezzapesa M, Martinelli A, Punzi V, Monti M, et al.
Blood Purif
. 2024 Feb;
53(5):396-404.
PMID: 38402859
Introduction: Acute kidney injury (AKI) is frequent in critically ill COVID-19 patients and is associated with a higher mortality risk. By increasing intrathoracic pressure, positive pressure ventilation (PPV) may reduce...
3.
Badagliacca R, Reali M, Poscia R, Pezzuto B, Papa S, Mezzapesa M, et al.
Int J Cardiol
. 2017 Mar;
234:128.
PMID: 28285628
No abstract available.
4.
Badagliacca R, Reali M, Poscia R, Pezzuto B, Papa S, Mezzapesa M, et al.
JACC Cardiovasc Imaging
. 2015 May;
8(6):642-52.
PMID: 25981504
Objectives: The aim of this study was to determine the prevalence of right intraventricular dyssynchrony, its determinants and prognostic impact in idiopathic, heritable, and anorexigen-induced pulmonary arterial hypertension. Background: Right...
5.
Badagliacca R, Poscia R, Pezzuto B, Nocioni M, Mezzapesa M, Francone M, et al.
J Heart Lung Transplant
. 2014 Dec;
34(3):395-403.
PMID: 25499139
Background: Although increased pulmonary pressure is caused by changes in the pulmonary vasculature, prognosis in idiopathic pulmonary arterial hypertension (IPAH) is strongly associated with right ventricular (RV) function. The aim...
6.
Badagliacca R, Poscia R, Pezzuto B, Papa S, Gambardella C, Francone M, et al.
J Heart Lung Transplant
. 2014 Aug;
34(3):381-9.
PMID: 25087105
Background: Right ventricular (RV) dyssynchrony has been described in pulmonary arterial hypertension (PAH), but no evidence is available on its morphologic determinants and its effect on systolic function. The aim...
7.
Riccieri V, Vasile M, Iannace N, Stefanantoni K, Sciarra I, Vizza C, et al.
Rheumatology (Oxford)
. 2013 May;
52(8):1525-8.
PMID: 23671125
Objective: Pulmonary arterial hypertension (PAH) is a complication of SSc due to increased vascular resistance, and abnormal vascularity is a well-known feature of the disease as shown by nailfold videocapillaroscopy...
8.
Badagliacca R, Poscia R, Pezzuto B, Papa S, Nona A, Mancone M, et al.
Cardiology
. 2012 Mar;
121(2):76-82.
PMID: 22433455
Objectives: Pulmonary arterial dilatation is considered a consequence of chronic pulmonary hypertension (PH), but despite its relatively common detection, its prevalence and prognostic impact have not yet been systematically investigated....