Disease: Cardiomyopathy dilated with conduction defect type 2
- Arrhythmogenic autoantibodies against calcium channel lead to sudden death in idiopathic dilated cardiomyopathy
- BET bromodomain inhibition attenuates cardiac phenotype in myocyte-specific lamin A/C-deficient mice
- Beta blockers prevent correlation of plasma ACE2 activity with echocardiographic parameters in patients with idiopathic dilated cardiomyopathy
- Beta-Blocker-Related Atrioventricular Conduction Disorders-A Single Tertiary Referral Center Experience
- Clinical manifestations and MRI features of Danon disease: a case series
- Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy
- Dilated Cardiomyopathy Phenotype-Associated Left Ventricular Noncompaction and Congenital Long QT Syndrome Type-2 in Infants With KCNH2 Gene Mutation: Anesthetic Considerations
- Echocardiographic pattern of left ventricular function recovery in tachycardia-induced cardiomyopathy patients
- Histological and proteomic profile of diabetic versus non-diabetic dilated cardiomyopathy
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- LMNA -Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-derived iPSC Differentiation Support Cell type and Lineage-specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-Derived Cells with Lami
- Long-Term Outcomes Among a Nationwide Cohort of Patients Using an Implantable Cardioverter-Defibrillator: UMBRELLA Study Final Results
- Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes
- Partial and complete loss of myosin binding protein H-like cause cardiac conduction defects
- Pre-excitation cardiac problems in children: recognition and treatment
- Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry
- Second-degree AV block type Mobitz I (Wenckebach) in a 49-year-old man with dilative cardiomyopathy
- Significance of sarcomere gene mutation in patients with dilated cardiomyopathy
- Sudden Unexpected Death after a mild trauma: The complex forensic interpretation of cardiac and genetic findings
- Survival Without Cardiac Transplantation Among Children With Dilated Cardiomyopathy
- TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy
- Two-dimensional speckle tracking imaging to assess the hazards of left ventricular function and ventricular wall motion disorders in children with pre-excitation syndrome and the efficacy of radiofrequency ablation treatment
- Usefulness of Serial N-terminal Pro-B-type Natriuretic Peptide Measurements to Predict Cardiac Death in Acute and Chronic Dilated Cardiomyopathy in Children
- Ventricular Tachycardia in a Patient With Dilated Cardiomyopathy Caused by a Novel Mutation of Lamin A/C Gene: Insights From Features on Electroanatomic Mapping, Catheter Ablation and Tissue Pathology