1. Myopathy due to a defect in muscle glycogen breakdown;McARDLE, B.;Clinical Science,1951
2. McArdle's syndrome: Phosphorylase deficient myopathy;MELLICK, R.S.; MAHLER, R.F.; HUGHES, B.P.;Lancet,1962
3. Defect in muscle phosphorylase: a newly defined human disease;PEARSON, C.M.; RIMMER, D.G.; MOMMAERTS, W.F.N.M.;Clinical Research,1959
4. Hereditary absence of muscle phosphorylase (McArdle's syndrome);SCHMID, R.; HAMMAKER, L.;New England Journal of Medicine,1961
5. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle;SCHMID, R.; MAHLER, R.;Journal of Clinical Investigation,1959