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Showing articles 0 to 10 of 10 Filter Applied: genetic diagnosis,prenatal (Click to remove) The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Huntingtons Disease BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease Neurol 44:288-290, Meiner,V.,et al, 1994 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 The Cerebrohepatorenal (Zellweger) Syndrome NEJM 310:1141-1146, Moser,A.E.,et al, 1984 CT Scans in Menkes Disease Neurol 29:304-312, Seay,A.R.,et al, 1979 Showing articles 0 to 10 of 10