Lista de obras -

A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation.

artículo científico publicado en 2016

A Prospective Study of Sudden Cardiac Death among Children and Young Adults

artículo científico publicado en 2016

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2016

ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy.

artículo científico publicado en 2016

Age makes a difference: Symptoms in pediatric supraventricular tachycardia

artículo científico publicado en 2018

An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia

scientific article published on 07 November 2018

Brugada syndrome caused by a large deletion in SCN5A only detected by multiplex ligation-dependent probe amplification

scientific article published on 02 February 2011

Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study

scientific article published on 10 September 2020

Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation.

artículo científico publicado en 2015

Clinical and genetic features of Australian families with long QT syndrome: A registry-based study.

artículo científico publicado en 2016

Clinical features and outcomes of childhood dilated cardiomyopathy: results from a national population-based study

artículo científico publicado en 2006

Clinical features and outcomes of childhood hypertrophic cardiomyopathy: results from a national population-based study

scientific article published on 22 August 2005

Clinical, electrocardiographic, and histologic correlations in children with dilated cardiomyopathy

artículo científico publicado en 2001

Delay to diagnosis amongst patients with catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2014

Establishment of an Australian National Genetic Heart Disease Registry.

artículo científico publicado en 2008

Excellent long-term functional outcome after an operation for anomalous left coronary artery from the pulmonary artery

artículo científico publicado en 1999

Factors influencing uptake of familial long QT syndrome genetic testing

artículo científico publicado en 2015

Long term somatic growth after repair of tetralogy of Fallot: evidence for restoration of genetic growth potential.

artículo científico publicado en 2003

Long-Term Outcomes of Childhood Left Ventricular Non-Compaction Cardiomyopathy: Results from a National Population-Based Study

artículo científico publicado en 2018

Long-Term Outcomes of Hypertrophic Cardiomyopathy Diagnosed During Childhood: Results From a National Population-Based Study

scientific article published on 28 February 2018

Long-term outcomes of dilated cardiomyopathy diagnosed during childhood: results from a national population-based study of childhood cardiomyopathy.

artículo científico publicado en 2013

Long-term results of anatomic correction for congenitally corrected transposition of the great arteries: A 19-year experience.

artículo científico publicado en 2017

Malignant pectus excavatum.

artículo científico publicado en 2006

Pediatric & Congenital Electrophysiology Society: building an international paediatric electrophysiology organisation.

artículo científico publicado en 2016

Pediatric & Congenital Electrophysiology Society: building an international paediatric electrophysiology organisation.

artículo científico publicado en 2016

Personalized arrhythmia prevention: do the I's have it?

artículo científico publicado en 2014

Perspectives in interventional electrophysiology in children and those with congenital heart disease: electrophysiology in children.

artículo científico

Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood

artículo científico publicado en 2017

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

artículo científico publicado en 2018

Successful ablation of refractory neonatal atrial flutter

artículo científico publicado en 2015

Successful implantation of a dual-chamber pacemaker in an ELBW infant for long QT syndrome

artículo científico publicado en 2014

Sudden Infant Death: QT or Not QT? That Is No Longer the Question

artículo científico publicado en 2016

Sudden death in childhood cardiomyopathy: results from a long-term national population-based study.

artículo científico publicado en 2015

Ten-year experience in atenolol use and exercise evaluation in children with genetically proven long QT syndrome

artículo científico publicado en 2017

The Epidemiology of Childhood Cardiomyopathy in Australia ⬇️

artículo científico publicado el 24 de abril de 2003

The QT and corrected QT interval in recovery after exercise in children

artículo científico publicado en 2011

The long QT syndrome and seizures in childhood.

artículo científico publicado en 1998

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy

scientific article published on 01 August 1999

The “surreptitious staphylococcus”staphylococcus lugdunensis endocarditis in a child

artículo científico publicado en 2002

Torsades de Pointes: 50 Years Later, Can We See It Coming?

artículo científico publicado en 2016

Transcatheter closure of perimembranous ventricular septal defect.

artículo científico publicado en 2007

Lista de obras de

A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation.

A Prospective Study of Sudden Cardiac Death among Children and Young Adults

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy.

Age makes a difference: Symptoms in pediatric supraventricular tachycardia

An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia

Brugada syndrome caused by a large deletion in SCN5A only detected by multiplex ligation-dependent probe amplification

Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study

Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation.

Clinical and genetic features of Australian families with long QT syndrome: A registry-based study.

Clinical features and outcomes of childhood dilated cardiomyopathy: results from a national population-based study

Clinical features and outcomes of childhood hypertrophic cardiomyopathy: results from a national population-based study

Clinical, electrocardiographic, and histologic correlations in children with dilated cardiomyopathy

Delay to diagnosis amongst patients with catecholaminergic polymorphic ventricular tachycardia

Establishment of an Australian National Genetic Heart Disease Registry.

Excellent long-term functional outcome after an operation for anomalous left coronary artery from the pulmonary artery

Factors influencing uptake of familial long QT syndrome genetic testing

Long term somatic growth after repair of tetralogy of Fallot: evidence for restoration of genetic growth potential.

Long-Term Outcomes of Childhood Left Ventricular Non-Compaction Cardiomyopathy: Results from a National Population-Based Study

Long-Term Outcomes of Hypertrophic Cardiomyopathy Diagnosed During Childhood: Results From a National Population-Based Study

Long-term outcomes of dilated cardiomyopathy diagnosed during childhood: results from a national population-based study of childhood cardiomyopathy.

Long-term results of anatomic correction for congenitally corrected transposition of the great arteries: A 19-year experience.

Malignant pectus excavatum.

Pediatric & Congenital Electrophysiology Society: building an international paediatric electrophysiology organisation.

Pediatric & Congenital Electrophysiology Society: building an international paediatric electrophysiology organisation.

Personalized arrhythmia prevention: do the I's have it?

Perspectives in interventional electrophysiology in children and those with congenital heart disease: electrophysiology in children.

Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

Successful ablation of refractory neonatal atrial flutter

Successful implantation of a dual-chamber pacemaker in an ELBW infant for long QT syndrome

Sudden Infant Death: QT or Not QT? That Is No Longer the Question

Sudden death in childhood cardiomyopathy: results from a long-term national population-based study.

Ten-year experience in atenolol use and exercise evaluation in children with genetically proven long QT syndrome

The Epidemiology of Childhood Cardiomyopathy in Australia ⬇️

The QT and corrected QT interval in recovery after exercise in children

The long QT syndrome and seizures in childhood.

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy

The “surreptitious staphylococcus”staphylococcus lugdunensis endocarditis in a child

Torsades de Pointes: 50 Years Later, Can We See It Coming?

Transcatheter closure of perimembranous ventricular septal defect.