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Andrea Nava
Andrea Nava
Professore Associato di Cardiologia, Università di Padova
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Anno
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria
FI Marcus, WJ McKenna, D Sherrill, C Basso, B Bauce, DA Bluemke, ...
Circulation 121 (13), 1533-1541, 2010
38042010
Arrhythmogenic right ventricular cardiomyopathy: dysplasia, dystrophy, or myocarditis?
C Basso, G Thiene, D Corrado, A Angelini, A Nava, M Valente
Circulation 94 (5), 983-991, 1996
2393*1996
Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology …
WJ McKenna, G Thiene, A Nava, F Fontaliran, C Blomstrom-Lundqvist, ...
British heart journal 71 (3), 215, 1994
21601994
Right ventricular cardiomyopathy and sudden death in young people
G Thiene, A Nava, D Corrado, L Rossi, N Pennelli
New England Journal of Medicine 318 (3), 129-133, 1988
20591988
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study
D Corrado, C Basso, G Thiene, WJ McKenna, MJ Davies, F Fontaliran, ...
Journal of the American College of Cardiology 30 (6), 1512-1520, 1997
12471997
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
N Tiso, DA Stephan, A Nava, A Bagattin, JM Devaney, F Stanchi, ...
Human molecular genetics 10 (3), 189-194, 2001
10472001
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy
A Rampazzo, A Nava, S Malacrida, G Beffagna, B Bauce, V Rossi, ...
The American Journal of human genetics 71 (5), 1200-1206, 2002
8142002
Sudden death in young competitive athletes: clinicopathologic correlations in 22 cases
D Corrado, G Thiene, A Nava, L Rossi, N Pennelli
The American journal of medicine 89 (5), 588-596, 1990
7991990
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy
K Pilichou, A Nava, C Basso, G Beffagna, B Bauce, A Lorenzon, G Frigo, ...
Circulation 113 (9), 1171-1179, 2006
7052006
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
A Nava, B Bauce, C Basso, M Muriago, A Rampazzo, C Villanova, ...
Journal of the American College of Cardiology 36 (7), 2226-2233, 2000
6142000
Familial occurrence of right ventricular dysplasia: a study involving nine families
A Nava, G Thiene, B Canciani, R Scognamiglio, L Daliento, G Buja, ...
Journal of the American College of Cardiology 12 (5), 1222-1228, 1988
5321988
Regulatory mutations in transforming growth factor-β3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1
G Beffagna, G Occhi, A Nava, L Vitiello, A Ditadi, C Basso, B Bauce, ...
Cardiovascular research 65 (2), 366-373, 2005
5192005
Comparison of QT dispersion in hypertrophic cardiomyopathy between patients with and without ventricular arrhythmias and sudden death
G Buja, M Miorelli, P Turrini, P Melacini, A Nava
The American journal of cardiology 72 (12), 973-976, 1993
5121993
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: need for an international registry
D Corrado, G Fontaine, FI Marcus, WJ McKenna, A Nava, G Thiene, ...
Circulation 101 (11), e101-e106, 2000
4982000
Ventricular fibrillation without apparent heart disease: description of six cases
B Martini, A Nava, G Thiene, GF Buja, B Canciani, R Scognamiglio, ...
American heart journal 118 (6), 1203-1209, 1989
4851989
The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23–q24
A Rampazzo, A Nava, GA Danieli, G Buja, L Daliento, G Fasoli, ...
Human molecular genetics 3 (6), 959-962, 1994
4591994
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations
B Bauce, C Basso, A Rampazzo, G Beffagna, L Daliento, G Frigo, ...
European heart journal 26 (16), 1666-1675, 2005
3722005
Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy
T Xu, Z Yang, M Vatta, A Rampazzo, G Beffagna, K Pillichou, SE Scherer, ...
Journal of the American College of Cardiology 55 (6), 587-597, 2010
3492010
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies
C Basso, E Czarnowska, MD Barbera, B Bauce, G Beffagna, ...
European heart journal 27 (15), 1847-1854, 2006
348*2006
Right bundle branch block, right precordial ST-segment elevation, and sudden death in young people
D Corrado, C Basso, G Buja, A Nava, L Rossi, G Thiene
Circulation 103 (5), 710-717, 2001
3452001
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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