Evaluation of genetic causes of cardiomyopathy in childhood

Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging

(2015) Animesh Tandon et al.   AMERICAN JOURNAL OF CARDIOLOGY

Propionic acidemia in a previously healthy adolescent with acute onset of dilated cardiomyopathy

(2014) Alexander Laemmle et al.   EUROPEAN JOURNAL OF PEDIATRICS

Inborn errors of metabolism identified via newborn screening: Ten-year incidence data and costs of nutritional interventions for research agenda planning

(2014) Bradford L. Therrell et al.   MOLECULAR GENETICS AND METABOLISM

Risk stratification at diagnosis for children with hypertrophic cardiomyopathy: an analysis of data from the Pediatric Cardiomyopathy Registry

(2013) Steven E Lipshultz et al.   LANCET

Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: A study from the Pediatric Cardiomyopathy Registry

(2012) James D. Wilkinson et al.   AMERICAN HEART JOURNAL

Pediatric Cardiomyopathy: Importance of Genetic and Metabolic Evaluation

(2012) Steven J. Kindel et al.   JOURNAL OF CARDIAC FAILURE

Cardiomyopathy in Friedreich Ataxia

(2012) R. Mark Payne et al.   JOURNAL OF CHILD NEUROLOGY

Uptake of Cardiac Screening and Genetic Testing Among Hypertrophic and Dilated Cardiomyopathy Families

(2012) Erin M. Miller et al.   Journal of Genetic Counseling

Noonan syndrome and clinically related disorders

(2011) Marco Tartaglia et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

(2011) Michael J. Ackerman et al.   HEART RHYTHM

Inherited Cardiomyopathies

(2011) Hugh Watkins et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genetic diagnostics and genetic counselling in Hypertrophic Cardiomyopathy (HCM)

(2011) I.M. van Langen   Netherlands Heart Journal

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

(2010) P. Charron et al.   EUROPEAN HEART JOURNAL

Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines

(2010) A. A. Romano et al.   PEDIATRICS

The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years

(2010) James D. Wilkinson et al.   Heart Failure Clinics

Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic Cardiomyopathy

(2009) Juan Pablo Kaski et al.   Circulation-Cardiovascular Genetics

Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

(2009) Ray E. Hershberger et al.   JOURNAL OF CARDIAC FAILURE

Unusual presentation of propionic acidaemia as isolated cardiomyopathy

(2009) T. M. Lee et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

(2009) J. Martijn Bos et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Cardiomyopathy in newborns and infants: a broad spectrum of aetiologies and poor prognosis

(2008) Andrea Badertscher et al.   ACTA PAEDIATRICA

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

(2008) J P Kaski et al.   HEART