A 27-Year Old Man with Rapidly Progressive Coma
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Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I 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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Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
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Inherited Metabolic Diseases of the Nervous System, Maple Syrup Urine Disease
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Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008
Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007
Phenylketonuria
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Aromatic L-Amino Acid Decarboxylase Deficiency
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Coma in a Young Anorexic Woman
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Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
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Reye's Syndrome 30 Years On, Possible Marker of Inherited Metabolic Disorders
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Neurologic Crises in Hereditary Tyrosinemia
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GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
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