Spremljaj
Andrea Mazzanti
Andrea Mazzanti
Cardiologist, Fondazione S. Maugeri
Preverjeni e-poštni naslov na icsmaugeri.it
Naslov
Navedeno
Navedeno
Leto
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with …
Authors/Task Force Members, SG Priori, C Blomström-Lundqvist, ...
Ep Europace 17 (11), 1601-1687, 2015
57332015
Dilated cardiomyopathy
HP Schultheiss, DL Fairweather, ALP Caforio, F Escher, RE Hershberger, ...
Nature reviews Disease primers 5 (1), 32, 2019
6882019
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
4892020
Desmoplakin cardiomyopathy, a fibrotic and inflammatory form of cardiomyopathy distinct from typical dilated or arrhythmogenic right ventricular cardiomyopathy
ED Smith, NK Lakdawala, N Papoutsidakis, G Aubert, A Mazzanti, ...
Circulation 141 (23), 1872-1884, 2020
3612020
Long-term follow-up of patients with short QT syndrome
C Giustetto, R Schimpf, A Mazzanti, C Scrocco, P Maury, O Anttonen, ...
Journal of the American College of Cardiology 58 (6), 587-595, 2011
3602011
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
3432020
Programmed ventricular stimulation for risk stratification in the Brugada syndrome: a pooled analysis
J Sroubek, V Probst, A Mazzanti, P Delise, JC Hevia, K Ohkubo, A Zorzi, ...
Circulation 133 (7), 622-630, 2016
2792016
Novel insight into the natural history of short QT syndrome
A Mazzanti, A Kanthan, N Monteforte, M Memmi, R Bloise, V Novelli, ...
Journal of the American College of Cardiology 63 (13), 1300-1308, 2014
2622014
Gene-specific therapy with mexiletine reduces arrhythmic events in patients with long QT syndrome type 3
A Mazzanti, R Maragna, A Faragli, N Monteforte, R Bloise, M Memmi, ...
Journal of the American College of Cardiology 67 (9), 1053-1058, 2016
2502016
Arrhythmogenic right ventricular cardiomyopathy: clinical course and predictors of arrhythmic risk
A Mazzanti, K Ng, A Faragli, R Maragna, E Chiodaroli, N Orphanou, ...
Journal of the American College of Cardiology 68 (23), 2540-2550, 2016
2082016
Interplay between genetic substrate, QTc duration, and arrhythmia risk in patients with long QT syndrome
A Mazzanti, R Maragna, G Vacanti, N Monteforte, R Bloise, M Marino, ...
Journal of the American College of Cardiology 71 (15), 1663-1671, 2018
1962018
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome
N Lahrouchi, R Tadros, L Crotti, Y Mizusawa, PG Postema, L Beekman, ...
Circulation 142 (4), 324-338, 2020
1292020
ESC Scientific Document Group. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for …
SG Priori, C Blomström-Lundqvist, A Mazzanti, N Blom, M Borggrefe, ...
Eur Heart J 36 (41), 2793-2867, 2015
1092015
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ...
Nature genetics 54 (3), 232-239, 2022
1032022
Guía ESC 2015 sobre el tratamiento de pacientes con arritmiasventriculares y prevención de la muerte súbita cardiaca
SG Priori, C Blomström-Lundqvist, A Mazzanti, N Blom, M Borggrefe, ...
Revista Española de Cardiología 69 (2), 2016
91*2016
Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain
D García-Giustiniani, M Arad, M Ortíz-Genga, R Barriales-Villa, ...
Heart 101 (13), 1047-1053, 2015
882015
Allele-specific silencing of mutant mRNA rescues ultrastructural and arrhythmic phenotype in mice carriers of the R4496C mutation in the ryanodine receptor gene (RYR2)
R Bongianino, M Denegri, A Mazzanti, F Lodola, A Vollero, ...
Circulation research 121 (5), 525-536, 2017
852017
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ...
Genetics in medicine 23 (1), 47-58, 2021
822021
The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases
A Mazzanti, S O’Rourke, K Ng, C Miceli, G Borio, A Curcio, F Esposito, ...
Expert review of cardiovascular therapy 12 (4), 499-519, 2014
802014
Hydroquinidine prevents life-threatening arrhythmic events in patients with short QT syndrome
A Mazzanti, R Maragna, G Vacanti, A Kostopoulou, M Marino, ...
Journal of the American College of Cardiology 70 (24), 3010-3015, 2017
792017
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