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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Angiokeratoma Corporis Diffusum
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Molybdenum Cofactor Deficiency
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Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures
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Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
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Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome
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Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
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Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
Neurol 39:847-848, Kolodny,E.H., 1989
Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
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Bilateral Lucency of the Globus Pallidus Complicating Methylmalonic Acidemia
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Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
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Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
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Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
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Corneal Opacification in Infancy
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Metabolic Defects Associated with Mental Retardation
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