Determination of Brain Death
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Clinicopathologic Conference,Aceruloplasminemia, Hereditary
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Toxidrome Recognition in Chemical - Weapons Attacks
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Diagnosis of Reversible Causes of Coma
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Management of Cerebellar Infarction With Mass Effect
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Neurosurgical Management of Cerebellar Haematoma and Infarct
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
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Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
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Ethanol and the Nervous System
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Cranial Nerve Deficit:A Clue to the Diagnosis of Ethylene Glycol Poisoning
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Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
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