Peroxisomal Disorders

J Gordon Millichap

doi:10.15844/pedneurbriefs-2-11-5

Peroxisomal Disorders

Pediatric Neurology Briefs

Volume 2 (1988): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1988

Abstract

The biochemical and clinical diagnostic characteristics of peroxisomal disorders are reviewed by authors from the Department of Pediatrics, Medical University of South Carolina, Charleston, SC.

References

Singh I Johnson GH Brown FR 3rd Peroxisomal disorders. Biochemical and clinical diagnostic considerations Am J Dis Child 1988 Dec 142 12 1297 301 10.1001/archpedi.1988.02150120051039 3057865
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Moser HW The peroxisome: nervous system role of a previously underrated organelle. The 1987 Robert Wartenberg lecture Neurology 1988 Oct 38 10 1617 27 10.1212/WNL.38.10.1617 2458548
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Britton TC Gibberd FB A family with heredopathia atactica polyneuritiformis (Refsum’s disease) J R Soc Med 1988 Oct 81 10 602 3 2460625
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-2-11-5 | Journal eISSN: 2166-6482

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Language: English

Page range: 84 - 85

Published on: Nov 1, 1988

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Clinical Diagnostic Characteristics,

Neonatal Adrenoleukodystrophy,

Peroxisomal Enzymatic Defects

© 1988 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 2 (1988): Issue 11