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Neurological Deterioration in Young Adults with Phenylketonuria
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Inherited Metabolic Diseases of the Nervous System, Maple Syrup Urine Disease
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Neurological Findings in Aminoacylase 1 Deficiency
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Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria
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Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease
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Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
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Diagnosis of Treatable Wilson's Disease
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Glycine Encephalopathy
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A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
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CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977
Possible Pathophysiology of Neurologic Abnormalities assoc. with Nonketotic hyperglycinemia
NEJM 294:1295, Ramson,B.R., 1976
Pediatric Neurology
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Encephalomyelopathy of Leigh
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