• A case report of Danon's disease with dilated phenotype
• A Frequent Observation of Wolff-Parkinson-White Syndrome and Fasciculoventricular Pathways in Patients With Danon Disease
• A Pathogenic LAMP2 Non-Canonical Splice Site Mutation Caused Danon Disease Requiring Heart Transplantation
• A rare and fatal cause of hypertrophic cardiomyopathy: Danon disease
• Altered Splicing of <em>LAMP2</em> in a Multigenerational Family from Latvia Affected by Danon Disease
• Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease
• Autophagy guided interventions to modify the cardiac phenotype of Danon disease
• Beyond vacuolar pathology: Multiomic profiling of Danon disease reveals dysfunctional mitochondrial homeostasis
• Clinical characteristics of Danon disease
• Clinical features of pediatric Danon disease and the importance of early diagnosis
• Clinical manifestations and MRI features of Danon disease: a case series
• Danon disease manifesting as dilated cardiomyopathy in a 37-year-old woman
• DANON DISEASE: A MODEL OF PHOTORECEPTOR DEGENERATION SECONDARY TO PRIMARY RETINAL PIGMENT EPITHELIUM DISEASE
• Danon Disease: Entire <em>LAMP2</em> Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the Literature
• Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the Literature
• Danon disease: Rare cause of cardiomyopathy
• Editorial commentary: Highlighting the ray of hope in Danon disease research after 40 years
• Effect of pharmacological heart failure drugs and gene therapy on Danon's cardiomyopathy
• Endovascular treatment in Danon disease: a case report
• Glycogen Storage Disease
• Glycogen Storage Disease
• Glycogen synthase downregulation rescues the amylopectinosis of murine RBCK1 deficiency
• High prevalence of paraspinal muscle involvement in adults with McArdle disease
• Hypertrophic Cardiomyopathy versus Storage Diseases with Myocardial Involvement
• Identification and functional analysis of a novel de novo missense mutation located in the initiation codon of LAMP2 associated with early onset female Danon disease
• Identification of a novel splicing-altering LAMP2 variant in a Chinese family with Danon disease
• International Consensus on Differential Diagnosis and Management of Patients With Danon Disease: JACC State-of-the-Art Review
• Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
• Metabolic Maturation Exaggerates Abnormal Calcium Handling in a <em>Lamp2</em> Knockout Human Pluripotent Stem Cell-Derived Cardiomyocyte Model of Danon Disease
• Metabolic Maturation Exaggerates Abnormal Calcium Handling in a Lamp2 Knockout Human Pluripotent Stem Cell-Derived Cardiomyocyte Model of Danon Disease
• Multimodal imaging in Danon disease
• Myocardial Strain and Association With Clinical Outcomes in Danon Disease: A Model for Monitoring Progression of Genetic Cardiomyopathies
• Myocardial Tissue Characterization in Danon Disease
• New deletion in <em>LAMP2</em> causing familial Danon disease. Effect of the X-chromosome inactivation
• New deletion in LAMP2 causing familial Danon disease. Effect of the X-chromosome inactivation
• Paediatric hypertrophic cardiomyopathy secondary to Danon disease
• Right Ventricle Involvement by Glycogen Storage Cardiomyopathy (PRKAG2): Standard and Advanced Echocardiography Analyses