• A case report of delayed diagnosis of danon disease: Caused by a newly recognized mutation in the lysosome-associated membrane protein-2 gene
• A Frequent Observation of Wolff-Parkinson-White Syndrome and Fasciculoventricular Pathways in Patients With Danon Disease
• A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy
• A novel LAMP2 mutation associated with severe cardiac hypertrophy and microvascular remodeling in a female with Danon disease: a case report and literature review
• A novel ZC4H2 gene mutation, K209N, in Japanese siblings with arthrogryposis multiplex congenita and intellectual disability: characterization of the K209N mutation and clinical findings
• A systematic review of the biological, social, and environmental determinants of intellectual disability in children and adolescents
• Arrhythmias and fasciculoventricular pathways in patients with Danon disease: A single center experience
• Cardiac arrhythmias in patients with Danon disease
• Clinical features of pediatric Danon disease and the importance of early diagnosis
• Clinical Findings and Prognosis of Danon Disease. An Analysis of the Spanish Multicenter Danon Registry
• Clinical manifestations and MRI features of Danon disease: a case series
• Clinical, electrocardiographic, and electrophysiologic characteristics of patients with a fasciculoventricular pathway: the role of PRKAG2 mutation
• Danon disease as a cause of concentric left ventricular hypertrophy in patients who underwent endomyocardial biopsy
• Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children
• Danon disease caused by two novel mutations of the LAMP2 gene: implications for two ends of the clinical spectrum
• Danon disease: a case report and literature overview
• Danon disease: a rare cause of left ventricular hypertrophy with cardiac magnetic resonance follow-up
• Danon disease: focusing on heart
• Early onset of cardiomyopathy and intellectual disability in a girl with Danon disease associated with a de novo novel mutation of the LAMP2 gene
• Familial ring (20) chromosomal mosaicism
• Fasciculoventricular and atrioventricular accessory pathways in patients with Danon disease and preexcitation: A multicenter experience
• Glycogen storage disease: danon syndrome
• Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing
• Ischemic stroke due to hypoperfusion in a patient with a previously unrecognized Danon disease
• New variant of phenylketonuria with progressive neurological illness unresponsive to phenylalanine restriction
• Phenotypic spectrum and genetics of SCN2A-related disorders, treatment options, and outcomes in epilepsy and beyond
• Progression of Danon disease with medical imaging: two case reports
• Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation)
• Review: Danon disease: Review of natural history and recent advances
• STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy
• Sudden death associated with danon disease in women
• Synaptic remodelling and elimination as integral processes of synaptogenesis
• Treatment of depression in an adolescent with cardiomyopathy and arrhythmia
• Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?
• Wolff Parkinson white pattern in Danon disease: When preexcitation is not what it seems
• Wolff-Parkinson-White syndrome and concentric left ventricular hypertrophy in a teenager: Danon disease
• Wolff-Parkinson-White's syndrome and Danon's disease