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Showing articles 0 to 8 of 8 Filter Applied: genetic diagnosis,prenatal (Click to remove) 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 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy JNNP 63:4-14, vanGeel,B.M.,et al, 1997 GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients Ann Neurol 31:328-332, Yoshida,K.,et al, 1992 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Showing articles 0 to 8 of 8