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Alessandra Rampazzo
Alessandra Rampazzo
Professore di Biologia applicata, Dipartimento di Biologia, Università degli Studi di Padova
Email verificata su unipd.it
Titolo
Citata da
Citata da
Anno
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
10462001
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
8122002
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
7042006
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
6132000
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
5162005
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
3712005
Diagnosis of arrhythmogenic cardiomyopathy: the Padua criteria
D Corrado, MP Marra, A Zorzi, G Beffagna, A Cipriani, M De Lazzari, ...
International journal of cardiology 319, 106-114, 2020
3592020
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
3482010
A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42–q43
A Rampazzo, A Nava, P Erne, M Eberhard, E Vian, P Slomp, N Tiso, ...
Human molecular genetics 4 (11), 2151-2154, 1995
2951995
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers
B Bauce, A Rampazzo, C Basso, A Bagattin, L Daliento, N Tiso, P Turrini, ...
Journal of the American College of Cardiology 40 (2), 341-349, 2002
2942002
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
2932006
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis
D Corrado, PJ Van Tintelen, WJ McKenna, RNW Hauer, A Anastastakis, ...
European heart journal 41 (14), 1414-1429, 2020
2852020
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene–related arrhythmogenic right ventricular cardiomyopathy
I Rigato, B Bauce, A Rampazzo, A Zorzi, K Pilichou, E Mazzotti, F Migliore, ...
Circulation: Cardiovascular Genetics 6 (6), 533-542, 2013
2672013
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm
A Rampazzo, A Nava, M Miorin, P Fonderico, B Pope, N Tiso, B Livolsi, ...
Genomics 45 (2), 259-263, 1997
2281997
Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy
J van Hengel, M Calore, B Bauce, E Dazzo, E Mazzotti, M De Bortoli, ...
European heart journal 34 (3), 201-210, 2013
2242013
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
B Bauce, A Nava, G Beffagna, C Basso, A Lorenzon, G Smaniotto, ...
Heart rhythm 7 (1), 22-29, 2010
2182010
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women
B Bauce, G Frigo, FI Marcus, C Basso, A Rampazzo, F Maddalena, ...
The American journal of cardiology 102 (9), 1252-1257, 2008
1292008
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43
B Bauce, A Nava, A Rampazzo, L Daliento, M Muriago, C Basso, ...
The American journal of cardiology 85 (5), 573-579, 2000
1182000
Arrhythmogenic right ventricular cardiomyopathy a still underrecognized clinic entity
G Thiene, C Basso, GA Danieli, A Rampazzo, D Corrado, A Nava
Trends in cardiovascular medicine 7 (3), 84-90, 1997
1181997
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
Articoli 1–20