Carlo Napolitano
Carlo Napolitano
University of Pavia and Molecular Cardiology ICS Maugeri, Pavia, Italy
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Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias
PJ Schwartz, SG Priori, C Spazzolini, AJ Moss, GM Vincent, C Napolitano, ...
Circulation 103 (1), 89-95, 2001
Risk stratification in the long-QT syndrome
SG Priori, PJ Schwartz, C Napolitano, R Bloise, E Ronchetti, M Grillo, ...
New England Journal of Medicine 348 (19), 1866-1874, 2003
CaV1. 2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
I Splawski, KW Timothy, LM Sharpe, N Decher, P Kumar, R Bloise, ...
Cell 119 (1), 19-31, 2004
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
SG Priori, C Napolitano, N Tiso, M Memmi, G Vignati, R Bloise, ...
Circulation 103 (2), 196-200, 2001
Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
SG Priori, C Napolitano, M Memmi, B Colombi, F Drago, M Gasparini, ...
Circulation 106 (1), 69-74, 2002
Natural history of Brugada syndrome: insights for risk stratification and management
SG Priori, C Napolitano, M Gasparini, C Pappone, P Della Bella, ...
Circulation 105 (11), 1342-1347, 2002
Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome
AJ Moss, W Zareba, WJ Hall, PJ Schwartz, RS Crampton, J Benhorin, ...
Circulation 101 (6), 616-623, 2000
Low penetrance in the long-QT syndrome: clinical impact
SG Priori, C Napolitano, PJ Schwartz
Circulation 99 (4), 529-533, 1999
Long QT Syndrome Patients With Mutations of the SCN5A and HERG Genes Have Differential Responses to Na+ Channel Blockade and to Increases in Heart …
PJ Schwartz, SG Priori, EH Locati, C Napolitano, F Cantù, JA Towbin, ...
Circulation 92 (12), 3381-3386, 1995
Influence of the genotype on the clinical course of the long-QT syndrome
W Zareba, AJ Moss, PJ Schwartz, GM Vincent, JL Robinson, SG Priori, ...
New England Journal of Medicine 339 (14), 960-965, 1998
FKBP12. 6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death
XHT Wehrens, SE Lehnart, F Huang, JA Vest, SR Reiken, PJ Mohler, ...
Cell 113 (7), 829-840, 2003
A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 Gene
SG Priori, SV Pandit, I Rivolta, O Berenfeld, E Ronchetti, A Dhamoon, ...
Circulation research 96 (7), 800-807, 2005
Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome
PJ Schwartz, SG Priori, M Cerrone, C Spazzolini, A Odero, C Napolitano, ...
Circulation 109 (15), 1826-1833, 2004
Association of long QT syndrome loci and cardiac events among patients treated with β-blockers
SG Priori, C Napolitano, PJ Schwartz, M Grillo, R Bloise, E Ronchetti, ...
Jama 292 (11), 1341-1344, 2004
Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry
SG Priori, M Gasparini, C Napolitano, P Della Bella, AG Ottonelli, ...
Journal of the American College of Cardiology 59 (1), 37-45, 2012
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: a prospective evaluation of 52 families
SG Priori, C Napolitano, M Gasparini, C Pappone, P Della Bella, ...
Circulation 102 (20), 2509-2515, 2000
Age-and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry
EH Locati, W Zareba, AJ Moss, PJ Schwartz, GM Vincent, MH Lehmann, ...
Circulation 97 (22), 2237-2244, 1998
Spectrum of ST-T–wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes
L Zhang, KW Timothy, GM Vincent, MH Lehmann, J Fox, LC Giuli, J Shen, ...
Circulation 102 (23), 2849-2855, 2000
Dispersion of the QT interval. A marker of therapeutic efficacy in the idiopathic long QT syndrome.
SG Priori, C Napolitano, L Diehl, PJ Schwartz
Circulation 89 (4), 1681-1689, 1994
Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice
C Napolitano, SG Priori, PJ Schwartz, R Bloise, E Ronchetti, J Nastoli, ...
Jama 294 (23), 2975-2980, 2005
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