J. Crosson

Publications55
h-index22
Citations1,864
Highly Influential Citations60
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Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases.
A group of relatively uncommon but important genetic cardiovascular diseases (GCVDs) are associated with increased risk for sudden cardiac death during exercise, including hypertrophic… Expand
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PACES/HRS expert consensus statement on the evaluation and management of ventricular arrhythmias in the child with a structurally normal heart.
and Management of Ventricular Arrhythmias in the Child With a Structurally Normal Heart Jane E. Crosson, MD, FACC (Chair), David J. Callans, MD, FHRS, FACC, FAHA (Chair), David J. Bradley, MD, FACC,… Expand
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Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
OBJECTIVES The aim of this study was to assess the outcome of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) patients treated with an implantable cardioverter-defibrillator (ICD).… Expand
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Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.
The underlying genetic etiology of rhabdomyolysis remains elusive in a significant fraction of individuals presenting with recurrent metabolic crises and muscle weakness. Using exome sequencing, we… Expand
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Placement of implantable cardioverter‐defibrillators in paediatric and congenital heart defect patients: a pipeline for model generation and simulation prediction of optimal configurations
•  Implantable cardioverter‐defibrillators (ICDs) with transvenous leads often cannot be implanted in a standard manner in paediatric and congenital heart defect (CHD) patients. Currently, there is… Expand
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Infantile Restrictive Cardiomyopathy Resulting From a Mutation in the Cardiac Troponin T Gene
Here we report the first infantile case of restrictive cardiomyopathy caused by a de novo mutation of the cardiac troponin T gene. The patient presented with an apparent life-threatening event. She… Expand
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The relevance of prolonged QTc measurement to pediatric psychopharmacology.
OBJECTIVE To consider the relevance of prolonged QTc (QT interval corrected for rate) to pediatric psychopharmacology. METHOD The authors reviewed publications on QTc prolongation and publications… Expand
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Endocardial and epicardial steroid lead pacing in the neonatal and paediatric age group
Aim: To compare the performance of steroid eluting epicardial and endocardial leads in infants and children requiring permanent pacing. Methods: Evaluation of pacing and sensing characteristics,… Expand
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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset Disease.
OBJECTIVES The aims of this study were to determine the clinical characteristics and outcomes of pediatric-onset arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and to compare… Expand
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Novel and Highly Lethal NKX2.5 Missense Mutation in a Family With Sudden Death and Ventricular Arrhythmia
To date, several disease-related mutations in NKX2-5, a cardiac-specific homeobox gene, have been documented in patients with a variety of congenital heart diseases (CHDs). The most commonly reported… Expand
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