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Showing articles 0 to 6 of 6 Filter Applied: glycogen storage disease (Click to remove) McArdle's Disease:Biochemical and Molecular Genetic Studies Ann Neurol 24:774-781, Servidei,S.,et al, 1988 Phosphorylase Deficiency In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986 Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia Neurol 66:1585-1587, Fernandez,C.,et al, 2006 Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992 Adult Phosphorylase b Kinase Deficiency Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990 McArdle's Disease in the 1980s NEJM 312:370-371, Layzer,R.B., 1985 Showing articles 0 to 6 of 6