Mitochondrial Enzymes in Reye’s Syndrome

J Gordon Millichap

doi:10.15844/pedneurbriefs-5-12-9

Mitochondrial Enzymes in Reye’s Syndrome

Pediatric Neurology Briefs

Volume 5 (1991): Issue 12

By: J Gordon Millichap

Open Access

|Dec 1991

Abstract

A nonuniform decrease in several mitochondrial residual enzyme activities in the liver and brain of a 42 year old woman who died with Reye’s syndrome is reported from the Departments of Neurology and Pediatrics, Columbia Presbyterian Medical Center, New York, NY.

References

Van Coster RN De Vivo DC Blake D Lombes A Barrett R DiMauro S Adult Reye’s syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processing Neurology 1991 Nov 41 11 1815 1821 10.1212/WNL.41.11.1815 1944914
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Casteels-Van Daele M Management of childhood fever Lancet 1991 Nov 30 338 8779 1408 10.1016/0140-6736(91)92296-E 1682777
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-5-12-9 | Journal eISSN: 2166-6482

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Language: English

Page range: 95 - 96

Published on: Dec 1, 1991

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Mitochondrial Residual Enzyme,

Reye’s Syndrome,

Varicella

© 1991 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 5 (1991): Issue 12