Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Stefano, Bardari"'
Autor:
Martina, Nesti, Raimondo, Calvanese, Carlo, Pignalberi, Giosuè, Mascioli, Paolo, China, Giuseppe, Sgarito, Stefano, Bardari, Massimo, Zecchin
Publikováno v:
Giornale italiano di cardiologia (2006). 23(5)
Implantation of pacemakers and cardiac defibrillators is a life-saving treatment but can put our patients at risk of infections, increasing morbidity and mortality and prolonging hospitalization with a significant financial healthcare burden. A preve
Autor:
Massimo, Zecchin, Raimondo, Calvanese, Carlo, Pignalberi, Giosuè, Mascioli, Stefano, Bardari, Paolo, China, Giuseppe, Sgarito, Martina, Nesti
Publikováno v:
Giornale italiano di cardiologia (2006). 22(6)
Neuromuscular diseases (NMD) are a broadly defined group of disorders that all involve injury or dysfunction of peripheral nerves, neuromuscular junction or muscle, often with dominant or recessive pattern of inheritance. Cardiac involvement is uncom
Autor:
Davide Stolfo, Denise Zaffalon, Marco Merlo, Giulia Barbati, Gianfranco Sinagra, Massimo Zecchin, Stefano Bardari, Alessandro Altinier
Publikováno v:
Journal of Cardiovascular Medicine. 20:450-458
Objective The objective was to provide an exhaustive characterization of ECG features in a large cohort of dilated cardiomyopathies (DCMs) and then investigate their possible prognostic role in the long term. Background ECG is an accessible, reproduc
Publikováno v:
The Arrhythmic Patient in the Emergency Department ISBN: 9783319243269
Acute metabolic disorders are relatively common amongst medical and surgical patients, especially in the critically ill. Whilst increasing the complexity of management plans, these circumstances also increase the risk of cardiac complications, such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37c960f2961fb8b4aae8edc13fc6fd87
https://doi.org/10.1007/978-3-319-24328-3_9
https://doi.org/10.1007/978-3-319-24328-3_9
Publikováno v:
Genetic Cardiomyopathies ISBN: 9788847027565
Arrhythmias and/or conduction defects can complicate some types of cardiomyopathy (CMP) and might represent a useful clue to a specific gene defect (Table 3.1). The presence of these arrhythmias can be important from a diagnostic point of view becaus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ccf2fccf5f5f3dfa66ab95ac38181bd
http://hdl.handle.net/11368/2905252
http://hdl.handle.net/11368/2905252