Clinicopathologic Conference,Aceruloplasminemia, Hereditary
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
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Autosomal Dominant Acute Necrotizing Encephalopathy
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Coma in a Young Anorexic Woman
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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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Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
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