Glycogen Storage Disease Type 5 Latest Advances
Find the Latest Research About Glycogen Storage Disease Type 5
Last Updated: 09/26/2026
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Found 288 publications
A Diagnostic Conundrum: Atypical McArdle Disease Mimic With Heterozygous PYGM Mutation and Cytochrome C Oxidase (COX)-Negative Fibers.
Journal: Cureus
Published: May 27, 2026
The Impact of Muscle Fatigue on McArdle Disease: A Case Report.
Journal: Cureus
Published: February 09, 2026
An exercise intervention in children and young adults with McArdle disease: feasibility, acceptability, and clinical outcomes.
Journal: Orphanet journal of rare diseases
Published: September 18, 2025
Coexistence of McArdle disease and hypokalemic periodic paralysis: A case report.
Journal: Medicina clinica
Published: August 21, 2025
When Fatigue Hides A Metabolic Myopathy: A Case Report of Mcardle Disease with Molecular Diagnosis.
Journal: European journal of case reports in internal medicine
Published: August 17, 2025
Lactate-induced mitochondrial magnesium uptake and its metabolic implications in the McArdle disease model.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: August 14, 2025
Muscle Biopsy as a Decisive Tool in a Pediatric Case with Overlapping Genetic Findings for McArdle Disease and Dystrophinopathy.
Journal: Klinische Padiatrie
Published: August 11, 2025
Acute kidney injury after swimming: a pediatric case of McArdle disease.
Journal: Pediatric nephrology (Berlin, Germany)
Published: February 27, 2025
Glycogen storage disease type V: delayed diagnosis of a cause of exercise intolerance in a patient with hereditary haemorrhagic telangiectasia.
Journal: BMJ case reports
Published: February 20, 2025
A disease that is difficult to predict: regional distribution and phenotypic, histopathological and genetic findings in McArdle disease.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: December 28, 2024
Last Updated: 09/26/2026