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Birth Defects Original Article Series|February 1, 1971
Glycogen storage diseases of muscle problems in biochemical geneticsL P Rowland, S Dimauro, W J BankThe New England Journal of Medicine|February 27, 1975
A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferaseW J Bank, S DiMauro, E Bonilla, et al.Archives of Neurology|March 1, 1976
Urinary excretion of carnitine in Duchenne muscular dystrophyS DiMauro, L P RowlandAnnals of Neurology|January 1, 1978
McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzymeS DiMauro, S Arnold, A Miranda, et al.Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegiaL P Rowland, M Hirano, S DiMauro, et al.Archives of Neurology|October 1, 1984
Clinical varieties of neuromuscular disease in debrancher deficiencyF Cornelio, N Bresolin, P A Singer, et al.Muscle & Nerve|May 1, 1987
High serum levels of creatine kinase: asymptomatic prelude to distal myopathyG Galassi, L P Rowland, A P Hays, et al.Annals of Neurology|March 1, 1981
Glycogen debrancher deficiency is reproduced in muscle cultureA F Miranda, S DiMauro, A Antler, et al.Annals of Neurology|October 1, 1984
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndromeS G Pavlakis, P C Phillips, S DiMauro, et al.Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.Pageof 44