1. Myoglobin and muscular dystrophy;Rowland, L.P.; Dunne, P.B.; Penn, A.S.; Maher, E.;Arch Neurol,1968
2. Clinical syndromes associated with ragged red fibers;Rowland, L.P.; Blake, D.M.; Hirano, M.;Rev Neurol,1991
3. Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis;Larsson, L.-E.; Linderholm, H.; Muller, R.; Ringqvist, T.; Sornas, R.;Jf Neurol Neurosurg Psychiatry,1964
4. McArdle's disease presenting as convulsions and rhabdomyolysis;Salmon, S.E.; Turner, C.E.;Am Jf Med,1965
5. Familial recurrent rhabdomyolysis due to carnitine palmityltransferase deficiency;Patten, B.M.; Wood, J.M.; Harati, Y.; Hefferan, P.; Howell, R.R.;Am Jf Med,1979