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Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
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Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 54-Year-Old Woman with Progressive Headache and Neurologic Decline
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Clinicopath Conf, Infantile Krabbe Disease
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Glycogen-Storage Disease Type II
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Neurological Presentation of Fabry's Disease in a 52 Year Old Man
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Inborn Errors of Urea Synthesis
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Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
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Adult Phosphorylase b Kinase Deficiency
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
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Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
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Glycine Encephalopathy
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