Disease: Myopathy- McArdle type
- A case of McArdle disease: efficacy of vitamin B6 on fatigability and impaired glycogenolysis
- 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)
- 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
- Identification of retinoic acid in a high content screen for agents that overcome the anti-myogenic effect of TGF-beta-1
- 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 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
- Overexpression of HSP10 in skeletal muscle of transgenic mice prevents the age-related fall in maximum tetanic force generation and muscle Cross-Sectional Area
- 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
- 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