• A first in literature: anesthesia management in kidney transplant surgery of a patient with McArdle disease
• Acute ketone supplementation in the absence of muscle glycogen utilization: Insights from McArdle disease
• An autosomal recessive variant in PYGM causes myophosphorylase deficiency in Red Angus composite cattle
• An experiment of nature links muscle glycogen unavailability with very high fat oxidation rates despite low aerobic fitness
• Atraumatic Acute Paraspinal Compartment Syndrome in a Patient With McArdle's Disease
• Can a modified ketogenic diet be a nutritional strategy for patients with McArdle disease? Results from a randomized, single-blind, placebo-controlled, cross-over study
• Carbohydrate Ingestion before Exercise for Individuals with McArdle Disease: Survey Evidence of Implementation and Perception in Real-World Settings
• Cardiac comorbidities in McArdle disease: case report and systematic review
• Clinical and Laboratory Findings on Glycogen Storage Disease Type V: Results from a Retrospective Observational Study in a Tertiary Hospital
• Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation
• Development of Continuum of Care for McArdle disease: A practical tool for clinicians and patients
• Diagnosis and genetic analysis of a case with glycogen storage disease type V caused by compound heterozygous mutations in the PYGM gene
• Diagnostic accuracy and the first genotype-phenotype correlation in glycogen storage disease type V
• Dose-response effect of pre-exercise carbohydrates under muscle glycogen unavailability: Insights from McArdle disease
• Exercise induced muscle weakness in a young adult: McArdle's disease unusual presentation
• Fatigue and associated factors in 172 patients with McArdle disease: An international web-based survey
• Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology
• Glycogen storage disease type V: a still under-recognized condition lacking definitive genotype-phenotype correlates
• Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?
• McArdle disease in a patient with anorexia nervosa: a case report
• McArdle's disease in four pediatric patients. Diagnostic algorithm for exercise intolerance
• McArdle's disease revealed by acute low back pain
• Metabolic adaptations in McArdle's disease and its mechanisms
• Metabolic aspects of glycogenolysis with special attention to McArdle disease
• Metabolic Myopathies in the Era of Next-Generation Sequencing
• Muscle glycogen unavailability and fat oxidation rate during exercise: Insights from McArdle disease
• New perspectives for the treatment and follow-up of glycogen storage disease type V: DL-3-hydroxybutyric acid with modified Atkins diet and quadriceps femoris shear wave elastography
• Patient-Reported Experiences with a Low-Carbohydrate Ketogenic Diet: An International Survey in Patients with McArdle Disease
• Population-based incidence rates of 15 neuromuscular disorders: a nationwide capture-recapture study in the Netherlands
• Powerless muscles in McArdle disease - what general practitioners should know
• Recurrent atraumatic compartment syndrome as a manifestation of genetic neuromuscular disease
• Repeated oral sucrose dosing after the second wind is unnecessary in patients with McArdle disease: Results from a randomized, placebo-controlled, double-blind, cross-over study
• Rhabdomyolysis in McArdle disease caused by scuba diving
• Rhabdomyolysis of rare etiology
• Syndromic PRD: case report of McArdle retinopathy and review of literature
• Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life
• Valuing Mundane Manifestations of Rare, but Underdiagnosed, Diseases in Portugal: The Example of McArdle Disease