Lista de obras - Silvia Castelletti - Dominio Público Uruguay

A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: Validation of the 2013 diagnostic criteria

artículo científico publicado en 2014

A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome

artículo científico publicado en 2018

Ablation Compared to Drug Therapy for Recurrent Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy; Results from a Multicenter Study

article

Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk

scientific article published on 20 March 2020

Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy ⬇️

artículo científico publicado en 2015

Advanced Arrhythmogenic Cardiomyopathy in Former Marathon Runner

artículo científico publicado en 2018

An instantaneous ECV with no blood sampling: using native blood T1 for hematocrit is as good as standard ECV.

artículo científico publicado en 2015

Arrhythmogenic right ventricular cardiomyopathy in Boxer dogs: the diagnosis as a link to the human disease.

artículo científico publicado en 2017

Automatic Measurement of the Myocardial Interstitium: Synthetic Extracellular Volume Quantification Without Hematocrit Sampling

artículo científico

CMR detects abnormal septal convexity into the left ventricle in preclinical hypertrophic cardiomyopathy

Cardiac Fabry Disease With Late Gadolinium Enhancement Is a Chronic Inflammatory Cardiomyopathy

artículo científico publicado en 2016

Clinical recommendations of cardiac magnetic resonance, Part I: ischemic and valvular heart disease: a position paper of the working group 'Applicazioni della Risonanza Magnetica' of the Italian Society of Cardiology

artículo científico publicado en 2017

Clinical recommendations of cardiac magnetic resonance, Part II: inflammatory and congenital heart disease, cardiomyopathies and cardiac tumors: a position paper of the working group 'Applicazioni della Risonanza Magnetica' of the Italian Society of

artículo científico publicado en 2017

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

artículo científico publicado en 2017

Diagnosis and management of hypertrophic cardiomyopathy

artículo científico publicado en 2015

Diagnostic Clues for the Diagnosis of Nonsarcomeric Hypertrophic Cardiomyopathy (Phenocopies): Amyloidosis, Fabry Disease, and Mitochondrial Disease

artículo científico publicado en 2018

Diffuse myocardial fibrosis - a therapeutic target? Proof of regression at 1-year following aortic valve replacement: the RELIEF-AS study.

artículo científico publicado en 2016

Electrocardiographic differentiation of idiopathic right ventricular outflow tract ectopy from early arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2017

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

artículo científico publicado en 2020

Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathy.

artículo científico publicado en 2015

EuroPrevent 2018, cardiovascular prevention at its highest levels

artículo científico publicado en 2018

Evolution in Managing Long QT Syndrome: From Registries to Centers of Excellence

artículo científico publicado en 2017

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

artículo científico publicado en 2020

From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2

scientific article published on 01 June 2019

From the last EuroPrevent towards the first ESC Preventive Cardiology Congress

artículo científico publicado en 2019

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1.

artículo científico publicado en 2018

Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics

scientific article published on 27 January 2019

Insight into hypertrophied hearts: a cardiovascular magnetic resonance study of papillary muscle mass and T1 mapping

artículo científico

Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

artículo científico

Left Ventricular Hypertrophy Revisited: Cell and Matrix Expansion Have Disease-Specific Relationships.

artículo científico publicado en 2017

Management of nonischemic-dilated cardiomyopathies in clinical practice: a position paper of the working group on myocardial and pericardial diseases of Italian Society of Cardiology

artículo científico publicado en 2020

Mexiletine Shortens the QT Interval in Patients With Potassium Channel-Mediated Type 2 Long QT Syndrome

scientific article published on 01 May 2019

Myocardial Edema, Myocyte Injury, and Disease Severity in Fabry Disease

artículo científico publicado en 2020

Myocardial T1 mapping

artículo científico publicado en 2015

Native T1 mapping in ATTR cardiac amyloidosis - comparison with AL cardiac amyloidosis - a 200 patient study.

artículo científico publicado en 2014

Native T1 mapping in transthyretin amyloidosis

artículo científico

Occult Transthyretin Cardiac Amyloid in Severe Calcific Aortic Stenosis: Prevalence and Prognosis in Patients Undergoing Surgical Aortic Valve Replacement

artículo científico

Partial Pericardial Agenesis Mimicking Arrhythmogenic Right Ventricular Cardiomyopathy

artículo científico publicado en 2019

Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy

artículo científico publicado en 2019

Recommendations for participation in leisure-time physical activity and competitive sports of patients with arrhythmias and potentially arrhythmogenic conditions. Part 2: ventricular arrhythmias, channelopathies, and implantable defibrillators

artículo científico publicado en 2020

Reference values of cardiac volumes, dimensions, and new functional parameters by MR: A multicenter, multivendor study

artículo científico publicado en 2016

Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentation

scientific article published on 01 May 2019

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

artículo científico publicado en 2020

Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

artículo científico publicado en 2012

T1 mapping in severe aortic stenosis: insights into LV remodeling.

artículo científico publicado en 2015

The Young Community of the European Association of Preventive Cardiology: The future in motion.

artículo científico publicado en 2018

The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

artículo científico publicado en 2017

The ventricular ectopic QRS interval (VEQSI): Diagnosis of arrhythmogenic right ventricular cardiomyopathy in patients with incomplete disease expression.

artículo científico publicado en 2016

To be, or not to be engaged in sport activities, that is the amletic question for patients with coronary artery disease

scientific article published on 04 October 2019

Lista de obras de Silvia Castelletti

A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: Validation of the 2013 diagnostic criteria

A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome

Ablation Compared to Drug Therapy for Recurrent Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy; Results from a Multicenter Study

Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk

Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy ⬇️

Advanced Arrhythmogenic Cardiomyopathy in Former Marathon Runner

An instantaneous ECV with no blood sampling: using native blood T1 for hematocrit is as good as standard ECV.

Arrhythmogenic right ventricular cardiomyopathy in Boxer dogs: the diagnosis as a link to the human disease.

Automatic Measurement of the Myocardial Interstitium: Synthetic Extracellular Volume Quantification Without Hematocrit Sampling

CMR detects abnormal septal convexity into the left ventricle in preclinical hypertrophic cardiomyopathy

Cardiac Fabry Disease With Late Gadolinium Enhancement Is a Chronic Inflammatory Cardiomyopathy

Clinical recommendations of cardiac magnetic resonance, Part I: ischemic and valvular heart disease: a position paper of the working group 'Applicazioni della Risonanza Magnetica' of the Italian Society of Cardiology

Clinical recommendations of cardiac magnetic resonance, Part II: inflammatory and congenital heart disease, cardiomyopathies and cardiac tumors: a position paper of the working group 'Applicazioni della Risonanza Magnetica' of the Italian Society of

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

Diagnosis and management of hypertrophic cardiomyopathy

Diagnostic Clues for the Diagnosis of Nonsarcomeric Hypertrophic Cardiomyopathy (Phenocopies): Amyloidosis, Fabry Disease, and Mitochondrial Disease

Diffuse myocardial fibrosis - a therapeutic target? Proof of regression at 1-year following aortic valve replacement: the RELIEF-AS study.

Electrocardiographic differentiation of idiopathic right ventricular outflow tract ectopy from early arrhythmogenic right ventricular cardiomyopathy.

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathy.

EuroPrevent 2018, cardiovascular prevention at its highest levels

Evolution in Managing Long QT Syndrome: From Registries to Centers of Excellence

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2

From the last EuroPrevent towards the first ESC Preventive Cardiology Congress

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1.

Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics

Insight into hypertrophied hearts: a cardiovascular magnetic resonance study of papillary muscle mass and T1 mapping

Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

Left Ventricular Hypertrophy Revisited: Cell and Matrix Expansion Have Disease-Specific Relationships.

Management of nonischemic-dilated cardiomyopathies in clinical practice: a position paper of the working group on myocardial and pericardial diseases of Italian Society of Cardiology

Mexiletine Shortens the QT Interval in Patients With Potassium Channel-Mediated Type 2 Long QT Syndrome

Myocardial Edema, Myocyte Injury, and Disease Severity in Fabry Disease

Myocardial T1 mapping

Native T1 mapping in ATTR cardiac amyloidosis - comparison with AL cardiac amyloidosis - a 200 patient study.

Native T1 mapping in transthyretin amyloidosis

Occult Transthyretin Cardiac Amyloid in Severe Calcific Aortic Stenosis: Prevalence and Prognosis in Patients Undergoing Surgical Aortic Valve Replacement

Partial Pericardial Agenesis Mimicking Arrhythmogenic Right Ventricular Cardiomyopathy

Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy

Recommendations for participation in leisure-time physical activity and competitive sports of patients with arrhythmias and potentially arrhythmogenic conditions. Part 2: ventricular arrhythmias, channelopathies, and implantable defibrillators

Reference values of cardiac volumes, dimensions, and new functional parameters by MR: A multicenter, multivendor study

Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentation

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.

T1 mapping in severe aortic stenosis: insights into LV remodeling.

The Young Community of the European Association of Preventive Cardiology: The future in motion.

The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

The ventricular ectopic QRS interval (VEQSI): Diagnosis of arrhythmogenic right ventricular cardiomyopathy in patients with incomplete disease expression.

To be, or not to be engaged in sport activities, that is the amletic question for patients with coronary artery disease