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The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauroExperimental Neurology|June 1, 1984
Multiple neutral maltase activities in normal and acid maltase-deficient human muscleS Shanske, N Bresolin, S DiMauroJournal of the Neurological Sciences|August 28, 1999
Disconnection of cerebellar Purkinje cells in Kearns-Sayre syndromeK Tanji, S DiMauro, E BonillaMuscle & Nerve. Supplement|January 1, 1995
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiencyS Tsujino, S Shanske, S DiMauroMuscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauroNeurology|November 1, 1987
Muscle energy metabolism in McArdle's syndrome by in vivo phosphorus magnetic resonance spectroscopyZ Argov, W J Bank, J Maris, et al.Neurology|November 1, 1976
Adenyl cyclase abnormality in Duchenne muscular dystrophy: muscle cells in cultureS Mawatari, A Miranda, L P RowlandPageof 44