Phenylketonuria
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Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
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Inherited Metabolic Diseases of the Nervous System, Galactosemia
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Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
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Cognitive Delay in a 7-year-old Girl
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Overview of Phenylketonuria
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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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Aromatic L-Amino Acid Decarboxylase Deficiency
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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Neurological Presentation of Fabry's Disease in a 52 Year Old Man
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Coma in a Young Anorexic Woman
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Diffusion-Weighted Imaging of White Matter Abnormalities in Patients with Phenylketonuria
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Dipsticks and Convulsions
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Inborn Errors of Urea Synthesis
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Clinicopath Conf
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
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Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
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Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
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Bone-Marrow Transplantation for Neurovisceral Storage Disorders
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