Cardiology Medical News about Cardiomyopathy, Hypertrophic

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Cardiomyopathy and Kidney Disease in a Patient with Maternally Inherited Diabetes and Deafness Caused by the 3243A>G Mutation of Mitochondrial DNA
Cardiology, 10/28/09

Azevedo O et al. – The authors discuss the possible mechanisms underlying the phenotypic variability and fluctuant clinical course of mitochondrial disorders and the potential usefulness of coenzyme Q10 and L–carnitine in 3243A>G mutation patients.

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Electrocardiographic amplitudes: a new risk factor for sudden death in hypertrophic cardiomyopathy
European Heart Journal, 11/10/09 Relevance Score: 68%

Severe Left Ventricular Wall Thinning and Extensive Fibrosis Without Evolution to End Stage Disease in a Patient With Hypertrophic Cardiomyopathy
Journal of The American Society of Echocardiography, 10/12/09 Relevance Score: 67%

Cell Cycle Re-Entry and Mitochondrial Defects in Myc-Mediated Hypertrophic Cardiomyopathy and Heart Failure
PLoS ONE - Cardiovascular Disorders, 10/02/09 Relevance Score: 67%

Severe Hypertrophic Cardiomyopathy in an Infant with a Novel PRKAG2 Gene Mutation: Potential Differences Between Infantile and Adult Onset Presentation
Pediatric Cardiology, 10/02/09 Relevance Score: 67%

Cardiomyopathy and anaesthesia
Continuing Education in Anaesthesia, Critical Care & Pain, 11/18/09 Relevance Score: 66%