• A first in literature: anesthesia management in kidney transplant surgery of a patient with McArdle disease
• A multi-parametric protocol to study exercise intolerance in McArdle's disease
• A novel compound heterozygous mutation in PYGM gene associated with McArdle's disease
• A pilot study of muscle plasma protein changes after exercise
• Absence of p.R50X <em>Pygm</em> read-through in McArdle disease cellular models
• Absence of p.R50X Pygm read-through in McArdle disease cellular models
• Acetylcholinesterase deficiency contributes to neuromuscular junction dysfunction in type 1 diabetic neuropathy
• Acute compartment syndrome: clinical course and laboratory findings in pregnant patients with McArdle's disease
• Acute pain control challenges with buprenorphine/naloxone therapy in a patient with compartment syndrome secondary to McArdle's disease: a case report and review
• An elderly diabetic patient with McArdle disease and recurrent rhabdomyolysis: a potential association with late hypoinsulinemia?
• Anesthesia in a Patient with McArdle Disease
• Atraumatic Acute Paraspinal Compartment Syndrome in a Patient With McArdle's Disease
• Can hyperuricemia predict glycogen storage disease (McArdle's disease) in rheumatology practice? (Myogenic hyperuricemia)
• Cardiac comorbidities in McArdle disease: case report and systematic review
• Clinical and laboratory features of patients with myophosphorylase deficiency (McArdle disease)
• Clinical and molecular characterization of McArdle's disease in Brazilian patients
• Clinical Presentation and Management of Severe Acute Renal Failure in McArdle Disease
• Creatine for treating muscle disorders
• Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
• Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)
• Detecting impaired muscle relaxation in myopathies with the use of motor cortical stimulation
• Development of Continuum of Care for McArdle disease: A practical tool for clinicians and patients
• Emotionally-intense situations can result in rhabdomyolysis in McArdle disease
• Exercise efficiency impairment in metabolic myopathies
• Exercise induced muscle weakness in a young adult: McArdle's disease unusual presentation
• Exercise testing-based algorithms to diagnose McArdle disease and MAD defects
• Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiency
• From exercise intolerance to functional improvement: the second wind phenomenon in the identification of McArdle disease
• Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry
• Heart rate and perceived muscle pain responses to a functional walking test in McArdle disease
• High prevalence of paraspinal muscle involvement in adults with McArdle disease
• Home-based aerobic exercise training improves skeletal muscle oxidative metabolism in patients with metabolic myopathies
• Identification of a novel PYGM mutation in a McArdle disease patient misdiagnosed as hypokalemic periodic paralysis
• Identification of patients with Pompé disease using routine pathology results: PATHFINDER (creatine kinase) study
• Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis
• Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency
• Investigating sodium valproate as a treatment for McArdle disease in sheep
• Knock-in mice for the R50X mutation in the PYGM gene present with McArdle disease
• Label-free identification of myopathological features with coherent anti-Stokes Raman scattering
• Long-term administration of the mitochondria-targeted antioxidant mitoquinone mesylate fails to attenuate age-related oxidative damage or rescue the loss of muscle mass and function associated with aging of skeletal muscle
• Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse model
• Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins
• Mastication and Oral Motor Function in McArdle Disease: Patient Reported Complaints
• McArdle Disease and Exercise Physiology
• McArdle Disease Misdiagnosed as Meningitis
• McArdle disease or glycogen storage disease type v: Should it affect anaesthetic management?
• McArdle Disease Presenting With Muscle Pain in a Teenage Girl: The Role of Whole-Exome Sequencing in Neurogenetic Disorders
• McArdle disease presenting with rhabdomyolisis and acute kidney injury
• McArdle Disease Rhabdomyolysis Precipitated by Acetazolamide for Idiopathic Intracranial Hypertension
• McArdle disease: 2 case reports
• McArdle disease: a case report and review
• McArdle disease: a unique study model in sports medicine
• McArdle Disease: New Insights into Its Underlying Molecular Mechanisms
• McArdle syndrome with recurrent rhabdomyolysis in a middle aged man
• MCARDLE'S DISEASE AND PHYSICAL ACTIVITY - A MIXED BLESSING
• McArdle's disease in four pediatric patients. Diagnostic algorithm for exercise intolerance
• McArdle's disease revealed by acute low back pain
• McArdle's disease: a clinical review and case report
• Metabolic aspects of glycogenolysis with special attention to McArdle disease
• Metabolic Myopathies in the Era of Next-Generation Sequencing
• Metabolic profiles of exercise in patients with McArdle disease or mitochondrial myopathy
• Monocarboxylate transporters and mitochondrial creatine kinase protein content in McArdle disease
• Muscle fiber type proportion and size is not altered in mcardle disease
• Muscle MRI in McArdle Disease: A European Multicenter Observational Study
• Myalgia during warming-up in a 12-year-old boy
• Neuropathic and Myopathic Pain
• New insights in the field of muscle glycogenoses
• Novel Asp511Thr mutation in McArdle disease with acute kidney injury caused by rhabdomyolysis
• Novel variant in the PYGM gene causing late-onset limb-girdle myopathy, ptosis, and camptocormia
• Oxidative stress and Nrf2 signaling in McArdle disease
• Phenotype and genotype of 197 British patients with McArdle disease: An observational single-centre study
• Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease
• Physical training for McArdle disease
• Recurrent atraumatic compartment syndrome as a manifestation of genetic neuromuscular disease
• Recurrent Compartment Syndrome Leading to the Diagnosis of McArdle Disease: Case Report
• Repeatedly in Rhabdomyolysis
• Resistance Exercise Training in McArdle Disease: Myth or Reality?
• Rhabdomyolysis Episode in an Individual with McArdle's Disease after Low Aerobic Exercise
• Rhabdomyolysis in McArdle disease caused by scuba diving
• Rhabdomyolysis of rare etiology
• Rhabdomyolysis With Acute Renal Failure Requiring Dialysis in McArdle Disease: A Role for the Antidepressant Venlafaxine?
• Severe axial myopathy in McArdle disease
• Single-centre experience on genotypic and phenotypic features of southern Brazilian patients with McArdle disease
• Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III
• Spectrum of metabolic myopathies
• Spontaneous Compartment Syndrome in a Patient with McArdle Disease: A Case Report and Review of the Literature
• Statins in hereditary myopathies: to give or not to give
• The "second wind" in McArdle's disease patients during a second bout of constant work rate submaximal exercise
• The effect of muscle glycogen phosphorylase (Pygm) knockdown on zebrafish morphology
• The investigation and management of metabolic myopathies
• The phenotypic and genotypic features of a Scottish cohort with McArdle disease
• The ratio of maximal handgrip force and maximal cycloergometry power as a diagnostic tool to screen for metabolic myopathies
• Therapeutic advances in the management of Pompe disease and other metabolic myopathies
• Total thyroidectomys in patient with McArdle's syndrome: Anesthetic management
• Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life
• Translational Medicine: Exercise Physiology Applied to Metabolic Myopathies
• Treatment of a high cardiovascular risk patient with McArdle's disease with PCSK9 inhibitors
• Unforeseen cardiac involvement in McArdle's disease
• Wave of renal impairment
• Whole-body muscle MRI in McArdle disease