subject area of
- A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle disease Academic Article
- Clinical Use of Creatine in Neuromuscular and Neurometabolic Disorders Academic Article
- Creatine treatment in muscle disorders: a meta-analysis of randomised controlled trials Academic Article
- Genetic risk factors associated with lipid-lowering drug-induced myopathies Academic Article
- Increased PFK activity and GLUT4 protein content in McArdle's disease Conference Paper
- Metabolic Myopathies Academic Article
- Monocarboxylate transporters and mitochondrial creatine kinase protein content in McArdle disease Academic Article
- Oxidative stress and Nrf2 signaling in McArdle disease Academic Article
- Peripheral nerve and vasculature involvement in myophosphorylase deficiency (mcardle’s disease) Academic Article
- Six novel mutations in the myophosphorylase gene in patients with McArdle disease and a family with pseudo-dominant inheritance pattern Academic Article