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