Disease: Cardiomyopathy dilated with conduction defect type 1
- A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes
- A novel gain-of-function mutation in SCN5A responsible for multifocal ectopic Purkinje-related premature contractions
- Association between LMNA mutation and familial and idiopathic dilated cardiomyopathy patients in Xinjiang
- Beta blockers prevent correlation of plasma ACE2 activity with echocardiographic parameters in patients with idiopathic dilated cardiomyopathy
- Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death
- Characteristics of ventricular tachycardia and long-term treatment outcome in patients with dilated cardiomyopathy complicated by lamin A/C gene mutations
- 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
- De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy
- Echocardiographic pattern of left ventricular function recovery in tachycardia-induced cardiomyopathy patients
- Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis
- Gene symbol: LMNA. Disease: Cardiomyopathy, dilated, with conduction defect 1
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- Lamin A molecular compression and sliding as mechanisms behind nucleoskeleton elasticity
- Long-Term Outcomes Among a Nationwide Cohort of Patients Using an Implantable Cardioverter-Defibrillator: UMBRELLA Study Final Results
- Myotonic dystrophy type 1 and high ventricular vulnerability at the electrophysiological evaluation: ICD yes or not?
- Neonatal lupus with left bundle branch block and cardiomyopathy: a case report
- Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defect
- Recovery of complete left bundle branch block in a dilated cardiomyopathy patient after treatment with sacubitril/valsartan: A case report
- Regional mapping of myocardial hibernation phenotype in idiopathic end-stage dilated cardiomyopathy
- Survival Without Cardiac Transplantation Among Children With Dilated Cardiomyopathy
- The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy
- Usefulness of Serial N-terminal Pro-B-type Natriuretic Peptide Measurements to Predict Cardiac Death in Acute and Chronic Dilated Cardiomyopathy in Children