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Showing articles 0 to 7 of 7 Filter Applied: enzyme,defect (Click to remove) Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 NEJM 370:911-920, Zhou, Q.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014 Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature Medicine 74:131-135, Felice,K.J.,et al, 1995 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 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency Ann Neurol 1:276, Karpati,G.,et al, 1977 Showing articles 0 to 7 of 7