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Alessandra Rampazzo
Alessandra Rampazzo
Professore di Biologia applicata, Dipartimento di Biologia, Università degli Studi di Padova
Verifierad e-postadress på unipd.it
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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
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
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
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
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
3602020
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
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
2962002
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
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
2872020
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
2252013
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
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Artiklar 1–20