Disease: Myopathy- X-linked- with excessive autophagy
- A Comprehensive Review of Autophagy and Its Various Roles in Infectious, Non-Infectious, and Lifestyle Diseases: Current Knowledge and Prospects for Disease Prevention, Novel Drug Design, and Therapy
- A new congenital form of X-linked autophagic vacuolar myopathy
- A novel form of autophagic vacuolar myopathy with late-onset and multiorgan involvement
- A novel vacuolar myopathy with dilated cardiomyopathy
- Altered <em>in vitro</em> muscle differentiation in X-linked myopathy with excessive autophagy
- Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy
- Autophagic vacuolar myopathy
- Autophagic vacuolar myopathy in twin girls
- Autophagic vacuolar pathology in desminopathies
- Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathies
- Cardiac autophagic vacuolation in severe X-linked myopathy with excessive autophagy
- Case of X-linked myopathy with excessive autophagy
- Congenital autophagic vacuolar myopathy is allelic to X-linked myopathy with excessive autophagy
- Congenital autophagic vacuolar myopathy is allelic to X-linked myopathy with excessive autophagy
- Diagnosing X-Linked Myopathy With Excessive Autophagy After 30 years: Genetic, Ultrasonographic, and Electrodiagnostic Findings
- Electrophysiological findings in X-linked myopathy with excessive autophagy
- Electrophysiology extends the phenotypic spectrum of X-linked myopathy with excessive autophagy
- Elevated urinary beta2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy
- Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy
- Eludication of pathomechanism of and development of therapy for autophagic vacuolar myopathies
- Fine-mapping the gene for X-linked myopathy with excessive autophagy
- Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesis
- Identification of a Novel Intronic Mutation in VMA21 Associated with a Classical Form of X-Linked Myopathy with Autophagy
- Infantile autophagic vacuolar myopathy is distinct from Danon disease
- LAMP-2 positive vacuolar myopathy with dilated cardiomyopathy
- Late adult-onset of X-linked myopathy with excessive autophagy
- Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28
- Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq
- Lysosomal myopathies: an excessive build-up in autophagosomes is too much to handle
- Muscle magnetic resonance imaging abnormalities in X-linked myopathy with excessive autophagy
- Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy
- Neuromuscular transmission defects in myopathies: Rare but worth searching for
- No cardiomyopathy in X-linked myopathy with excessive autophagy
- Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagy
- Novel Intronic Mutation in <em>VMA21</em> Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report
- Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case Report
- Phenotype variability and natural history of X-linked myopathy with excessive autophagy
- Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant
- Teaching neuroimages: hydroxychloroquine-induced vacuolar myopathy
- The spectrum of neurodevelopmental, neuromuscular and neurodegenerative disorders due to defective autophagy
- Treatment-responsive glycogen storage myopathy in a patient with POEMS syndrome: A new monoclonal gammopathy-associated myopathy
- VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification
- VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy
- VMA21 deficiency: a case of myocyte indigestion
- X-linked myopathy with excessive autophagy
- X-linked Myopathy with Excessive Autophagy - A Rare Cause of Vacuolar Myopathy in Children
- X-linked myopathy with excessive autophagy due to a mutation in VMA21 gene: the first case in China
- X-Linked Myopathy with Excessive Autophagy; A Case Report
- X-linked myopathy with excessive autophagy: a clinicopathological study of five new families
- X-linked myopathy with excessive autophagy: a failure of self-eating
- X-linked myopathy with excessive autophagy: a new hereditary muscle disease
- X-linked myopathy with excessive autophagy: First report of an Israeli family presenting with late onset lower limb girdle weakness
- X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene
- X-linked vacuolar myopathies: two separate loci and refined genetic mapping