Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Enrico, Gotti"'
Autor:
Giancarlo Casolo, Michele Massimo Gulizia, Daniela Aschieri, Alessandra Chinaglia, Marco Corda, Daniele Nassiacos, Salvatore Ivan Caico, Cristina Chimenti, Marzia Giaccardi, Enrico Gotti, Stefano Maffé, Roberta Magnano, Gianluca Solarino, Domenico Gabrielli, Fabrizio Oliva, Furio Colivicchi
Publikováno v:
European Heart Journal Supplements. 25:D294-D311
Extended risk stratification and optimal management of patients with a permanently increased risk of sudden cardiac death (SCD) are becoming increasingly important. There are several clinical conditions where the risk of arrhythmic death is present a
Publikováno v:
Applied Sciences, Vol 11, Iss 24, p 11779 (2021)
Metabolomic tecniques have already been used to characterize two of the most common coffee species, C. arabica and C. canephora, but no studies have focused on the characterization of green and roasted coffee varieties of a certain species. We aim to
Externí odkaz:
https://doaj.org/article/91f9bb38c7da4403bb1ec28f30c4033e
Autor:
A Albini, Enrico Gotti, F Pasca, D Guarino, Alessandra Manes, Massimiliano Palazzini, N Galie, A De Lorenzis, A Rinaldi, M Orzalkiewicz, Elisa Zuffa, Fabio Dardi, E Monti
Publikováno v:
European Heart Journal. 42
Background Pulmonary arterial hypertension (PAH) is a rare disease characterized by a complex remodeling of heart structures. Cardiac magnetic resonance (CMR) is the gold standard for a non-invasive evaluation of right ventricle (RV) volumes and mass
Autor:
Francesco, Saia, Fabio, Dardi, Nevio, Taglieri, Mariangela, Rotunno, Alessandra, Manes, Daniele, Guarino, Elisa, Zuffa, Alessandro, De Lorenzis, Ilenia, Magnani, Alberto, Ballerini, Fabio, Niro, Sofia, Martin Suarez, Davide, Pacini, Enrico, Gotti, Nazzareno, Galiè, Massimiliano, Palazzini
Publikováno v:
Giornale italiano di cardiologia (2006). 22(3 Suppl 1)
Balloon pulmonary angioplasty (BPA) represents a therapeutic option for the treatment of chronic thromboembolic pulmonary hypertension (CTEPH) in patients who are not eligible for surgical pulmonary endarterectomy (PEA) or with persistent/recurrent s
Autor:
A Rinaldi, Enrico Gotti, Nazzareno Galiè, A Albini, Alessandra Manes, Massimiliano Palazzini, Maria Letizia Bacchi Reggiani, Fabio Dardi, E Monti
Publikováno v:
European Journal of Heart Failure. 20:248-255
Aims Pulmonary hypertension (PH) is a relevant complication of left heart disease (LHD). The 2015 ESC/ERS PH guidelines report two different haemodynamic subsets of PH due to LHD (PH-LHD) based on levels of pulmonary vascular resistance (PVR) and dia
Autor:
Maria Letizia Bacchi Reggiani, Massimiliano Palazzini, Maria Barbara Leone, Nazzareno Galiè, Maurizio Zompatori, Sofia Martin Suarez, Marica Giannotta, Enrico Gotti, Mariano Cefarelli
Publikováno v:
La radiologia medica. 122:495-504
Our results confirm the diagnostic role of CTPA in evaluating patients with CTEPH and in addition open a new horizon in assessing hemodynamic changes in patients with CTEPH, only employing a CTPA, especially when RHC is contraindicated or not possibl
Autor:
A Rinaldi, Elisa Zuffa, A De Lorenzis, N Galie, Mariangela Rotunno, D Guarino, F Pasca, Fabio Dardi, I Magnani, Massimiliano Palazzini, Alessandra Manes, Enrico Gotti
Publikováno v:
European Heart Journal. 40
Background Current pulmonary hypertension (PH) guidelines stratify the risk of patients with pulmonary arterial hypertension (PAH) using a multiparametric approach. Anyway, the role of unmodifiable risk factors is not taken into account. Purpose The
Autor:
F Pasca, Mariangela Rotunno, Massimiliano Palazzini, Enrico Gotti, Elisa Zuffa, D Guarino, Andrea Rinaldi, Fabio Dardi, E Monti, Alessandro De Lorenzis, Nazzareno Galiè, I Magnani, Alessandra Manes
Publikováno v:
B55. USE YOUR ILLUSION I: CLINICAL RESEARCH IN PAH.
Current pulmonary arterial hypertension (PAH) guidelines stratify PAH patients risk with a multiparametric approach. Anyway, the role of unmodifiable risk factors is not taken into account. We evaluate the role of unmodifiable risk factors (age, gend
Autor:
Enrico Gotti, D Guarino, Mariangela Rotunno, F Pasca, Nazzareno Galiè, Alessandro De Lorenzis, I Magnani, Alessandra Manes, Massimiliano Palazzini, Elisa Zuffa, Andrea Cassani, Andrea Rinaldi, Fabio Dardi
Publikováno v:
B55. USE YOUR ILLUSION I: CLINICAL RESEARCH IN PAH.
Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) is very heterogeneous and there are few data on the effect of PAH-specific therapy except for patients with Eisenmenger's syndrome (ES) and PAH after defect correction
Autor:
Shigefumi Fukui, Satoshi Yasuda, Davide Pacini, Sofia Martin Suarez, Norifumi Nakanishi, Takeshi Ogo, Nazzareno Galiè, Alessandra Manes, Enrico Gotti, Massimiliano Palazzini
Publikováno v:
Pulmonary hypertension.
Background: It is reported that there is no benefit of pulmonary hypertensive medical therapy (PHT) in patients undergoing pulmonary endarterectomy (PEA), except improved total pulmonary resistance with epoprostenol (Kurt W et al. Circulation 2009).