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Showing articles 0 to 8 of 8 Filter Applied: enzyme,defect (Click to remove) Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 NEJM 370:911-920, Zhou, Q.,et al, 2014 Glycogen-Storage Disease Type II eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006 Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998 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 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Neurologic Crises in Hereditary Tyrosinemia NEJM 322:432-437, Mitchell,G.,et al, 1990 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families Hum Genet 70:347-354, Giugliani,R.,et al, 1985 Showing articles 0 to 8 of 8