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11 - Physician First, Scientist Second?

Published online by Cambridge University Press:  10 October 2023

Anna Huttenlocher
Affiliation:
University of Wisconsin, Madison
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Summary

Peter arrived as a new assistant professor of pediatric neurology at Yale University in 1966. This was in the midst of the Reye’s syndrome peak of the late 1960s. Reye’s syndrome is a life-threatening pediatric disease characterized by progressive brain and liver damage in children, often after a viral illness. It became a rare condition after epidemiological studies suggested a link between aspirin use in children and the onset of Reye’s syndrome after a viral illness. The reduced rates of Reye’s syndrome are largely attributable to public health messaging to limit aspirin use in children, but until that change, it often fell to pediatric neurologists to keep Reye’s syndrome patients alive.

Type
Chapter
Information
From Loss to Memory
Behind the Discovery of Synaptic Pruning
, pp. 69 - 76
Publisher: Cambridge University Press
Print publication year: 2023

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References

Huttenlocher, P. R.. Ketonemia and seizures: Metabolic and anticonvulsant effects of two ketogenic diets in childhood epilepsy. Pediatr Res 1976; 10: 536–40.CrossRefGoogle ScholarPubMed

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