Articles with public access mandates - Carlo NapolitanoLearn more
Not available anywhere: 4
Inherited calcium channelopathies in the pathophysiology of arrhythmias
L Venetucci, M Denegri, C Napolitano, SG Priori
Nature Reviews Cardiology 9 (10), 561-575, 2012
Mandates: Fondazione Telethon, Italy, British Heart Foundation, Fondazione Cariplo
Calmodulin kinase II inhibition prevents arrhythmias in RyR2R4496C+/− mice with catecholaminergic polymorphic ventricular tachycardia
N Liu, Y Ruan, M Denegri, T Bachetti, Y Li, B Colombi, C Napolitano, ...
Journal of molecular and cellular cardiology 50 (1), 214-222, 2011
Mandates: Fondazione Telethon, Italy
Flecainide and antiarrhythmic effects in a mouse model of catecholaminergic polymorphic ventricular tachycardia
N Liu, C Napolitano, LA Venetucci, SG Priori
Trends in cardiovascular medicine 22 (2), 35-39, 2012
Mandates: Fondazione Telethon, Italy, British Heart Foundation
Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy
A Curcio, A Malovini, A Mazzanti, M Memmi, P Gambelli, F La Rosa, ...
Heart Rhythm 18 (10), 1698-1706, 2021
Mandates: Government of Italy
Available somewhere: 60
Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome
I Goldenberg, AJ Moss, DR Peterson, S McNitt, W Zareba, ML Andrews, ...
Circulation 117 (17), 2184-2191, 2008
Mandates: US National Institutes of Health
Missense Mutations in Plakophilin-2 Can Cause Brugada Syndrome Phenotype By Decreasing Sodium Current and Na< sub> v</sub> 1.5 Membrane Localization
M Cerrone, X Lin, M Zhang, E Agullo-Pascual, A Pfenniger, ...
Heart Rhythm 10 (11), 1743, 2013
Mandates: US National Institutes of Health, Fondazione Telethon, Italy, Government of …
Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals
I Goldenberg, S Horr, AJ Moss, CM Lopes, A Barsheshet, S McNitt, ...
Journal of the American College of Cardiology 57 (1), 51-59, 2011
Mandates: US National Institutes of Health
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, CIRCULATIONAHA. 115.017885, 2016
Mandates: US National Institutes of Health, Fondazione Cariplo, Doris Duke Charitable …
SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes
CI Wu, PG Postema, E Arbelo, ER Behr, CR Bezzina, C Napolitano, ...
Heart rhythm 17 (9), 1456-1462, 2020
Mandates: Netherlands Organisation for Health Research and Development, Royal …
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
Mandates: Fondazione Telethon, Italy, Fondazione Cariplo, Government of Italy
European heart rhythm association (EHRA)/heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus …
AAM Wilde, C Semsarian, MF Márquez, AS Shamloo, MJ Ackerman, ...
Europace 24 (8), 1307-1367, 2022
Mandates: US National Institutes of Health, Research Foundation (Flanders), UK Medical …
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
Mandates: Government of Italy
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
Mandates: Government of Italy
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
Mandates: Government of Italy
Increased Ca2+ sensitivity of the ryanodine receptor mutant RyR2R4496C underlies catecholaminergic polymorphic ventricular tachycardia
M Fernández-Velasco, A Rueda, N Rizzi, JP Benitah, B Colombi, ...
Circulation research 104 (2), 201-209, 2009
Mandates: National Institute of Health and Medical Research, France
Long-QT syndrome after age 40
I Goldenberg, AJ Moss, J Bradley, S Polonsky, DR Peterson, S McNitt, ...
Circulation 117 (17), 2192-2201, 2008
Mandates: US National Institutes of Health
Catecholaminergic polymorphic ventricular tachycardia
C Napolitano, A Mazzanti, R Bloise, SG Priori
Mandates: European Commission
CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia
E Di Pasquale, F Lodola, M Miragoli, M Denegri, JE Avelino-Cruz, ...
Cell death & disease 4 (10), e843-e843, 2013
Mandates: Fondazione Telethon, Italy, Government of Italy
Risk factors for recurrent syncope and subsequent fatal or near-fatal events in children and adolescents with long QT syndrome
JF Liu, C Jons, AJ Moss, S McNitt, DR Peterson, M Qi, W Zareba, ...
Journal of the American College of Cardiology 57 (8), 941-950, 2011
Mandates: US National Institutes of Health
In the RyR2R4496C Mouse Model of CPVT, β-Adrenergic Stimulation Induces Ca Waves by Increasing SR Ca Content and Not by Decreasing the Threshold for Ca …
T Kashimura, SJ Briston, AW Trafford, C Napolitano, SG Priori, DA Eisner, ...
Circulation research 107 (12), 1483-1489, 2010
Mandates: Fondazione Telethon, Italy, British Heart Foundation
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