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Showing articles 0 to 7 of 7 Filter Applied: enzyme,defect (Click to remove) 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 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings Neurol 39:741-742, Friedman,J.H.,et al, 1989 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis Ann Neurol 18:614-617, Wolf,B.,et al, 1985 Subacute Necrotizing Encephalopathy in Late Adolescence Arch Neurol 18:478, Hardman,J.M.,et al, 1968 Showing articles 0 to 7 of 7