McArdle disease is a rare metabolic myopathy caused by a complete absence of the enzyme muscle glycogen phosphorylase. Affected people experience symptoms of fatigue and cramping within minutes of exercise and are at risk for acute muscle injury (rhabdomyolysis) and acute renal failure. If the first few minutes of exercise are paced, a 'second wind' will occur enabling exercise to continue. This is due to mobilisation and utilisation of alternative fuel substrates. Aerobic training appears to improve work capacity by increasing cardiovascular fitness. To assess the effects of aerobic training in people with McArdle disease. We searched the Cochrane Neuromuscular Disease Group Specialized Register (11 January 2011), CENTRAL (2010, Issue 4), ...
We report the exercise capacity of an 8-year-old boy with clinical, histological, biochemical, and g...
Owing to the risk of severe rhabdomyolysis, clinicians advise McArdle disease patients to refrain fr...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
BACKGROUND: McArdle disease is a rare metabolic myopathy caused by a complete absence of the enzyme ...
McArdle disease is a metabolic myopathy mainly characterised by symptom onset during physical activi...
McArdle disease is due to an inborn defect in the muscle isoform of glycogen phosphorylase (or 'myop...
Patients with McArdle's disease commonly adopt a sedentary lifestyle. This sedentary behaviour, howe...
This study reports acute exercise responses in a large (N = 46) series of patients with McArdle dise...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
Kaur, P; Longhurst, G Waikato Institute of Technology Background: This is a case study of a 61 year ...
McArdle disease (also known as glycogen storage disease type V) is a pure myopathy caused by an inhe...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
McArdle disease (glycogen storage disease type V) is an inborn error of energy metabolism in the mus...
McArdle disease (glycogen storage disease Type V; MD) is a metabolic myopathy caused by a deficiency...
We report the exercise capacity of an 8-year-old boy with clinical, histological, biochemical, and g...
Owing to the risk of severe rhabdomyolysis, clinicians advise McArdle disease patients to refrain fr...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...
BACKGROUND: McArdle disease is a rare metabolic myopathy caused by a complete absence of the enzyme ...
McArdle disease is a metabolic myopathy mainly characterised by symptom onset during physical activi...
McArdle disease is due to an inborn defect in the muscle isoform of glycogen phosphorylase (or 'myop...
Patients with McArdle's disease commonly adopt a sedentary lifestyle. This sedentary behaviour, howe...
This study reports acute exercise responses in a large (N = 46) series of patients with McArdle dise...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
Kaur, P; Longhurst, G Waikato Institute of Technology Background: This is a case study of a 61 year ...
McArdle disease (also known as glycogen storage disease type V) is a pure myopathy caused by an inhe...
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to de...
McArdle disease is arguably the paradigm of exercise intolerance in humans. This disorder is caused ...
McArdle disease (glycogen storage disease type V) is an inborn error of energy metabolism in the mus...
McArdle disease (glycogen storage disease Type V; MD) is a metabolic myopathy caused by a deficiency...
We report the exercise capacity of an 8-year-old boy with clinical, histological, biochemical, and g...
Owing to the risk of severe rhabdomyolysis, clinicians advise McArdle disease patients to refrain fr...
McArdle's disease is a hereditary, metabolic myopathy characterized by weakness and muscle cramps af...