McArdle disease is due to an inborn defect in the muscle isoform of glycogen phosphorylase (or 'myophosphorylase'), the enzyme that catalyses the first step of glycogenolysis. This condition is still not fully understood and, while advances in research would help patients immeasurably, these would also enhance our understanding of exercise metabolism. It has been ten years since the first published report demonstrating the benefits of regular aerobic exercise for these patients. However, misconceptions remain and the value of exercise prescription for McArdle patients is still underlooked. Here we review the role of exercise in McArdle disease with the aim to better inform healthcare professionals and thus better serve the interests of pati...
A 9-year-old boy with McArdle disease, who demonstrated remarkable recovery of objectively measured ...
Kaur, P; Longhurst, G Waikato Institute of Technology Background: This is a case study of a 61 year ...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...
McArdle disease is a rare metabolic myopathy caused by a complete absence of the enzyme muscle glyco...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
McArdle disease (glycogen storage disease Type V; MD) is a metabolic myopathy caused by a deficiency...
McArdle disease is a metabolic myopathy mainly characterised by symptom onset during physical activi...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
McArdle disease (also known as glycogen storage disease type V) is a pure myopathy caused by an inhe...
McArdle disease (glycogen storage disease type V) is caused by inherited deficiency of a key enzyme ...
Patients with McArdle's disease commonly adopt a sedentary lifestyle. This sedentary behaviour, howe...
We report the exercise capacity of an 8-year-old boy with clinical, histological, biochemical, and g...
McArdle disease (glycogen storage disease type V, OMIM database number 232600) may provide the ultim...
McArdle disease (glycogen storage disease type V) is an inborn error of energy metabolism in the mus...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
A 9-year-old boy with McArdle disease, who demonstrated remarkable recovery of objectively measured ...
Kaur, P; Longhurst, G Waikato Institute of Technology Background: This is a case study of a 61 year ...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...
McArdle disease is a rare metabolic myopathy caused by a complete absence of the enzyme muscle glyco...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
McArdle disease (glycogen storage disease Type V; MD) is a metabolic myopathy caused by a deficiency...
McArdle disease is a metabolic myopathy mainly characterised by symptom onset during physical activi...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
McArdle disease (also known as glycogen storage disease type V) is a pure myopathy caused by an inhe...
McArdle disease (glycogen storage disease type V) is caused by inherited deficiency of a key enzyme ...
Patients with McArdle's disease commonly adopt a sedentary lifestyle. This sedentary behaviour, howe...
We report the exercise capacity of an 8-year-old boy with clinical, histological, biochemical, and g...
McArdle disease (glycogen storage disease type V, OMIM database number 232600) may provide the ultim...
McArdle disease (glycogen storage disease type V) is an inborn error of energy metabolism in the mus...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
A 9-year-old boy with McArdle disease, who demonstrated remarkable recovery of objectively measured ...
Kaur, P; Longhurst, G Waikato Institute of Technology Background: This is a case study of a 61 year ...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...