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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
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
Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
- A. Roguin, C. Bomma, +9 authors H. Calkins
- Journal of the American College of Cardiology
- 19 May 2004
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
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.
- S. Lalani, P. Liu, +48 authors Y. Yang
- Biology, Medicine
- American journal of human genetics
- 4 February 2016
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
Placement of implantable cardioverter‐defibrillators in paediatric and congenital heart defect patients: a pipeline for model generation and simulation prediction of optimal configurations
- L. J. Rantner, F. Vadakkumpadan, P. Spevak, J. Crosson, N. Trayanova
- The Journal of physiology
- 1 September 2013
• 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
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
The relevance of prolonged QTc measurement to pediatric psychopharmacology.
- M. Labellarte, J. Crosson, M. Riddle
- Journal of the American Academy of Child and…
- 1 June 2003
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
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
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset Disease.
- A. T. Te Riele, C. James, +13 authors H. Tandri
- JACC. Clinical electrophysiology
- 1 December 2015
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
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