Abnormal myelination in peroxisomal isolated dihydroxyacetone-phosphate acyltransferase deficiency
- 30 April 1997
- journal article
- research article
- Published by Elsevier in Pediatric Neurology
- Vol. 16 (3) , 232-236
- https://doi.org/10.1016/s0887-8994(97)00014-3
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delayJournal of Inherited Metabolic Disease, 1994
- Inborn errors and demyelination: MRI and the diagnosis of white matter diseaseJournal of Inherited Metabolic Disease, 1993
- Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorderJournal of Inherited Metabolic Disease, 1992
- The MR spectrum of peroxisomal disordersNeuroradiology, 1991
- Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primatesBrain & Development, 1989