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A 54-Year-Old Woman with Progressive Headache and Neurologic Decline
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
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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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Coma in a Young Anorexic Woman
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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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Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
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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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Detection of Urea Cycle Enzymopathies in Childhood
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Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
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Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
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Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
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Glycine Encephalopathy
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