Zobrazeno 1 - 10
of 614
pro vyhledávání: '"N Galie'"'
Autor:
A Spadotto, G Massaro, M Amadori, L Damaschin, C Martignani, M Ziacchi, M Biffi, N Galie, G Boriani, I Diemberger
Publikováno v:
Europace. 25
Funding Acknowledgements Type of funding sources: None. Background Recent ESC Atrial Fibrillation guidelines introduced some changes in the options for rate control, such as the possibility to combine beta-blockers (BB) and non-dihydropyridine calciu
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
М. Delcroix, А. Torbicki, D. Gopalan, O. Sitbon, F. A. Klok, I. Lang, D. Jenkins, N. H. Kim, M. Humbert, X. Jais, A. V. Noordegraaf, J. Pepke-Zaba, P. Brénot, P. Dorfmuller, E. Fadel, H.-A. Ghofrani, M. M. Hoeper, P. Jansa, M. Madani, H. Matsubara, T. Ogo, A. D’Armini, N. Galie, B. Meyer, P. Corkery, G. Meszaros, E. Mayer, G. Simonneau
Publikováno v:
PULMONOLOGIYA. 32:13-52
Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare complication of acute pulmonary embolism, either symptomatic or not. The occlusion of proximal pulmonary arteries by fibrotic intravascular material, in combination with a secondary micr
Autor:
M Garofalo, A Corsini, L Potena, M Schinzari, E Nardi, F Barberini, C Gargiulo, M Malaguti, M Sabatino, F Semprini, N Galie, S Nanni
Publikováno v:
European Heart Journal. 43
Background Despite controversial evidence, intra-aortic balloon pump (IABP) is still the most used temporary mechanical support in cardiogenic shock (CS), as a bridge to recovery or to more advanced mechanical support and/or heart transplantation [1]
Autor:
F Dardi, A Ballerini, D Guarino, F Donato, R Bertozzi, G Martini, I Magnani, A Manes, M Palazzini, N Galie'
Publikováno v:
European Heart Journal. 43
Background One of the most challenging differential diagnoses in pulmonary hypertension clinical practice, is the discrimination between idiopathic pulmonary arterial hypertension (IPAH) and pulmonary hypertension due to heart failure with preserved
Autor:
A Impellizzeri, S Amicone, M Armillotta, A Sansonetti, A Stefanizzi, F Angeli, M Fabrizio, F Bodega, L Canton, F P Tattilo, L Bergamaschi, A Foa', G Iannopollo, N Galie', C Pizzi
Publikováno v:
European Heart Journal. 43
Background Killip classification is a simple clinical tool for risk stratification in patients with acute myocardial infarction (AMI). However, predictors of high Killip class at admission and its prognostic role in myocardial infarction with non-obs
Autor:
V Parisi, M Graziosi, R Ditaranto, C Chiti, A G Caponetti, M Minnucci, R Baldassarre, F Di Nicola, C Catalano, G Saturi, A Berardini, F Pasquale, O Leone, N Galie', E Biagini
Publikováno v:
European Heart Journal. 43
Background Despite major advances, the recognition of arrhythmogenic left ventricular cardiomyopathy (ALVC) remains challenging, since this clinical entity is often concealed in different clinical settings both in terms of clinical onset and imaging
Autor:
M Armillotta, L Bergamaschi, S Amicone, A Sansonetti, A Stefanizzi, A Impellizzeri, F P Tattilo, F Angeli, M Fabrizio, P Paolisso, A Rinaldi, A Foa', G Casella, N Galie', C Pizzi
Publikováno v:
European Heart Journal. 43
Background Myocardial infarction with non-obstructive coronary arteries (MINOCA) represents a significant proportion of acute myocardial infarction (AMI) population. MINOCA is a working diagnosis and an accurate investigation of the underlying causes
Autor:
F Angeli, P Paolisso, I Magnani, M Fabrizio, A Rinaldi, M Armillotta, A Stefanizzi, S Amicone, F P Tattilo, N Suma, F Bodega, L Canton, N Galie, A Foa, C Pizzi
Publikováno v:
European Heart Journal. 43
Background Cardiac masses (CM) are an extremely heterogeneous clinical entity, including benign and malignant neoformations. 2D Echocardiography is nowadays the first-line approach to define nature and management of CM. Purpose The purpose of our stu
Autor:
F Di Nicola, R Ditaranto, F Barlocco, R Lillo, F Re, G Marchi, R Baldassarre, V Parisi, V Ferrara, C Chiti, J R Gimeno Blanes, F Graziani, N Galie', I Olivotto, E Biagini
Publikováno v:
European Heart Journal. 43
Background Anderson-Fabry disease (AFD) is an X-linked lysosomal storage disorder that have gained attention due to the availability of therapeutic options. Disease specific therapy (DST), either by enzyme replacement therapy or oral pharmacological