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The European cardiac resynchronization therapy survey

European heart journal, 2009-10, Vol.30 (20), p.2450-2460

2009

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Low penetrance in the long-QT Syndrome : Clinical impact

Circulation (New York, N.Y.), 1999-02, Vol.99 (4), p.529-533

1999

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CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia

Cell death & disease, 2013-10, Vol.4 (10), p.e843-e843

2013

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Genetics of sudden death: focus on inherited channelopathies

European heart journal, 2011-09, Vol.32 (17), p.2109-2118

2011

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Improving Wine Quality through Harvest Zoning and Combined Use of Remote and Soil Proximal Sensing

Soil Science Society of America journal, 2013-07, Vol.77 (4), p.1338-1348

2013

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Entomopathogenic nematodes as potential biological control agents of Popillia japonica (Coleoptera, Scarabaeidae) in Piedmont Region (Italy)

Journal of applied entomology (1986), 2018-04, Vol.142 (3), p.311-318

2018

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Outcome parameters for trials in atrial fibrillation: recommendations from a consensus conference organized by the German Atrial Fibrillation Competence NETwork and the European Heart Rhythm Association

Europace (London, England), 2007-11, Vol.9 (11), p.1006-1023

2007

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Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome

Circulation (New York, N.Y.), 2000-02, Vol.101 (6), p.616-623

2000

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Brugada syndrome and sudden cardiac death in children

The Lancet (British edition), 2000-03, Vol.355 (9206), p.808-809

2000

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A Molecular Link between the Sudden Infant Death Syndrome and the Long-QT Syndrome

The New England journal of medicine, 2000-07, Vol.343 (4), p.262-267

2000

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Using present and past climosequences to estimate soil organic carbon and related physical quality indicators under future climatic conditions

Agriculture, ecosystems & environment, 2018-11, Vol.266, p.17-30

2018

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Inherited Arrhythmogenic Diseases: The Complexity Beyond Monogenic Disorders

Circulation research, 2004-02, Vol.94 (2), p.140-145

Priori, Silvia G

2004

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Influence of the Genotype on the Clinical Course of the Long-QT Syndrome

The New England journal of medicine, 1998-10, Vol.339 (14), p.960-965

1998

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The elusive link between LQT3 and Brugada syndrome : The role of flecainide challenge

Circulation (New York, N.Y.), 2000-08, Vol.102 (9), p.945-947

2000

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome : ECG findings identify genotypes

Circulation (New York, N.Y.), 2000-12, Vol.102 (23), p.2849-2855

2000

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Short-term recovery of soil physical, chemical, micro- and mesobiological functions in a new vineyard under organic farming

Soil, 2015-01, Vol.1 (1), p.443-457

2015

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Proposed Diagnostic Criteria for the Brugada Syndrome

European heart journal, 2002-11, Vol.23 (21), p.1648-1654

2002

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Early Repolarization is Associated with Short QT Syndrome in Italian Cohort

Annals of global health, 2017-04, Vol.83 (1), p.183-183

2017

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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2001-01, Vol.103 (2), p.196-200

2001

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Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome

European heart journal, 2002-06, Vol.23 (12), p.975-983

2002

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Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome : Findings from the international LQTS registry

Circulation (New York, N.Y.), 1998-06, Vol.97 (22), p.2237-2244

1998

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FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Cell, 2003-06, Vol.113 (7), p.829-840

2003

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Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management parts I and II

Circulation (New York, N.Y.), 1999-02, Vol.99 (4), p.518-528

1999

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A Cardiac Arrhythmia Syndrome Caused by Loss of Ankyrin-B Function

Proceedings of the National Academy of Sciences - PNAS, 2004-06, Vol.101 (24), p.9137-9142

2004

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The European cardiac resynchronization therapy survey

Low penetrance in the long-QT Syndrome : Clinical impact

CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia

Genetics of sudden death: focus on inherited channelopathies

Outcome parameters for trials in atrial fibrillation: executive summary : Recommendations from a consensus conference organized by the German Atrial Fibrillation Competence NETwork (AFNET) and the European Heart Rhythm Association (EHRA)

Improving Wine Quality through Harvest Zoning and Combined Use of Remote and Soil Proximal Sensing

Entomopathogenic nematodes as potential biological control agents of Popillia japonica (Coleoptera, Scarabaeidae) in Piedmont Region (Italy)

Outcome parameters for trials in atrial fibrillation: recommendations from a consensus conference organized by the German Atrial Fibrillation Competence NETwork and the European Heart Rhythm Association

Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome

Brugada syndrome and sudden cardiac death in children

A Molecular Link between the Sudden Infant Death Syndrome and the Long-QT Syndrome

Using present and past climosequences to estimate soil organic carbon and related physical quality indicators under future climatic conditions

Inherited Arrhythmogenic Diseases: The Complexity Beyond Monogenic Disorders

Influence of the Genotype on the Clinical Course of the Long-QT Syndrome

The elusive link between LQT3 and Brugada syndrome : The role of flecainide challenge

Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome : ECG findings identify genotypes

Short-term recovery of soil physical, chemical, micro- and mesobiological functions in a new vineyard under organic farming

Proposed Diagnostic Criteria for the Brugada Syndrome

Early Repolarization is Associated with Short QT Syndrome in Italian Cohort

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome

Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome : Findings from the international LQTS registry

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management parts I and II

A Cardiac Arrhythmia Syndrome Caused by Loss of Ankyrin-B Function

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