All Stories

  1. ESCRT-III Component CHMP4C Attenuates Cardiac Hypertrophy by Targeting the Endo-Lysosomal Degradation of EGFR
  2. Gene-Echocardiography: Refining Genotype-Phenotype Correlations in Hypertrophic Cardiomyopathy
  3. Echocardiographic characteristics of PRKAG2 syndrome: a research using three-dimensional speckle tracking echocardiography compared with sarcomeric hypertrophic cardiomyopathy
  4. Identification of CHMP4C as a new risk gene for inherited dilated cardiomyopathy
  5. Right Ventricular Systolic Function and Cardiac Resynchronization Therapy
  6. Role of three-dimensional transesophageal echocardiography in transcatheter aortic valve implantation of bicuspid aortic valve stenosis: A controlled study and comparison with tricuspid aortic valve stenosis
  7. Whole exome sequencing revealed a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: patients showed biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, decreased exercise tolerance
  8. Whole-Exome Sequencing Identified a Novel Desmoglein-2 Gene Mutation Associated with Familial Arrhythmogenic Right Ventricular Cardiomyopathy
  9. Effect of Cardiac Resynchronization Therapy on Myocardial Fibrosis and Relevant Cytokines in a Canine Model With Experimental Heart Failure
  10. right ventricular systolic dysfunction in patients with obstructive sleep apnea
  11. “Pacing Bigeminal”