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Sweet success--a treatment for McArdle's disease.
Acid maltase deficiency and related myopathies.
Calf muscle mitochondrial and glycogenolytic ATP synthesis in patients with claudication due to peripheral vascular disease analysed using 31P magnetic resonance spectroscopy.
A 49-year-old woman with progressive shortness of breath.
Pompe disease: a review of the current diagnosis and treatment recommendations in the era of enzyme replacement therapy.
Electrodiagnostic evaluation of myopathies.
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.
Glycogen Storage Disease
Glycogen Storage Disease Type III
Glycogen Storage Disease Type V
Glycogen Storage Disease Type II
The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States.