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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia
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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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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
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Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
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Conditions That Mimic Stroke in the Emergency Department
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Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
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Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
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The Reversible Dementias:Do They Reverse?
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Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
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A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
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Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
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Bone-Marrow Transplantation for Neurovisceral Storage Disorders
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Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
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Angiokeratoma Corporis Diffusum
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