Sudden infant death syndrome: Organic acid profiles in cerebrospinal fluid from 47 children and the occurrence ofN‐acetylaspartic acid
- 1 May 1990
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (3), 330-332
- https://doi.org/10.1007/bf01799387
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Aspartoacylase Deficiency: The Enzyme Defect in Canavan DiseaseJournal of Inherited Metabolic Disease, 1989
- Aspartoacylase Deficiency: The Enzyme Defect in Canavan DiseasePublished by Springer Science and Business Media LLC ,1989
- N‐Acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophyJournal of Inherited Metabolic Disease, 1988
- Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year periodJournal of Mass Spectrometry, 1987
- N‐acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophyJournal of Inherited Metabolic Disease, 1986
- N-Acetylaspartic aciduria in a child with a progressive cerebral atrophyClinica Chimica Acta; International Journal of Clinical Chemistry, 1986