McArdle Disease and Exercise Physiology
Author:
Publisher
MDPI AG
Subject
General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology
Link
http://www.mdpi.com/2079-7737/3/1/157/pdf
Reference56 articles.
1. Myopathy due to a defect in muscle glycogen breakdown;McArdle;Clin. Sci.,1951
2. High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11;Lebo;Science,1984
3. Intron/exon structure of the human gene for the muscle isozyme of glycogen phosphorylase
4. Human Gene Mutation Database?A biomedical information and research resource
5. Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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1. Metabolic aspects of glycogenolysis with special attention to McArdle disease;Molecular Genetics and Metabolism;2024-08
2. Muscle glycogen unavailability and fat oxidation rate during exercise: Insights from McArdle disease;The Journal of Physiology;2022-11-29
3. Sea Bass Essence from Lates calcarifer Improves Exercise Performance and Anti-Fatigue in Mice;Metabolites;2022-06-08
4. Rhabdomyolysis Episode in an Individual with McArdle’s Disease after Low Aerobic Exercise;Saudi Journal of Kidney Diseases and Transplantation;2022-02
5. Effects of Perch Essence Supplementation on Improving Exercise Performance and Anti-Fatigue in Mice;International Journal of Environmental Research and Public Health;2022-01-20
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