Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Angela Pisani"'
Autor:
Hein Heidbuchel, Tony Reybrouck, Carina Blomström-Lundqvist, Michael Glikson, Per Ivar Hoff, William J. McKenna, Dorian Dugmore, Domenico Corrado, François Carré, Nicole M. Panhuyzen-Goedkoop, Antonio Spataro, Asle Hirth, Dieter Horstkotte, Andreas Hoffmann, Erik Hoffmann, Silvia G. Priori, Angela Pisani, Luc Vanhees, Pietro Delise, Deodato Assanelli, Antonio Pelliccia, Frank van-Buuren, Aris Anastassakis, Klaus Peter Mellwig, Jan Oudhof, Eloisa Arbustini, Jan Erik Nordrehaug, Erik Ekker Solberg, Gaetano Thiene, Mats Börjesson, Ellen Hoffmann, H H Björnstad, Robert Fagard, Maria Penco, Asterios Deligiannis, Uwe Dorwarth, Alessandro Biffi, Jeff Senden
A consensus document from the Study Group of Sports Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c837d18a21682eef4ef5bb7ea25a10d7
http://doc.rero.ch/record/302448/files/ehi325.pdf
http://doc.rero.ch/record/302448/files/ehi325.pdf
Autor:
Mario Mosconi, Luca Lanzarini, Isabella Torrente, Nicola Marziliano, Lorenzo Magrassi, M. Cristina Zoia, Andrea Pilotto, Maria Francesca Bedeschi, Daniela Larizza, Giulia Meloni, Elena Antoniazzi, Savina Mannarino, Silvia Ansaldi, Emanuele Porcu, A. Brega, Luigi Tavazzi, Maurizia Grasso, Clara Malattia, Eliana Disabella, Francesca Mari, Eloisa Arbustini, Angela Pisani
Publikováno v:
Università degli Studi di Siena-IRIS
Marfan Syndrome (MFS) is an autosomal dominant disorder of the connective tissue due to mutations of Fibrillin-1 gene (FBN1) in more than 90% of cases and Transforming Growth Factor-Beta-Receptor2 gene (TGFB2R) in a minority of cases. Genotyping is r
Publikováno v:
Italian heart journal. Supplement : official journal of the Italian Federation of Cardiology. 5(2)
The nuclear lamina is a proteinaceous layer apposed to the inner nuclear membrane. It is composed of a family of polypeptides, the lamins, highly conserved in evolution. In mammals, 3 lamins, A, B and C have been described with molecular weights rang
Publikováno v:
Italian heart journal. Supplement : official journal of the Italian Federation of Cardiology. 3(4)
The definition of familial dilated cardiomyopathy (DCM) is clinically based on the presence, in the same family, of at least two members proven as affected. The prevalence of familial forms is about 25-30%. The approach to define the prevalence of fa
Autor:
Matilde Todaro, John Ross, Stephen Trocha, Giacomo Frati, Angela Pisani, David J. Lefer, Matteo Antonio Russo, Yusu Gu, Roberta Roncarati, Claudio Napoli, Steven P. Jones, Carlo M. Croce, Giorgio Stassi, Gianluigi Condorelli, Alessandra Drusco
Up-regulation of proapoptotic genes has been reported in heart failure and myocardial infarction. To determine whether caspase genes can affect cardiac function, a transgenic mouse was generated. Cardiac tissue-specific overexpression of the proapopt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2bcedf25feacdc3b226aea1cb7aec95
https://europepmc.org/articles/PMC55563/
https://europepmc.org/articles/PMC55563/
Autor:
Iolanda Enea, Angela Pisani, Massimo Volpe, C Tritto, Maria A.E. Rao, Alessandro F. Mele, Mario Condorelli
Publikováno v:
Journal of cardiac failure. 1(5)
One of the main goals of modern management and care of heart failure is to prevent the disease to progress toward congestion and death. The achievement of such an objective may, in fact, guarantee a sufficient quality of life and reduce the exposure