Portal de Periódicos da CAPES

Sudden infant death syndrome: Organic acid profiles in cerebrospinal fluid from 47 children and the occurrence of N ‐acetylaspartic acid

1990; Springer Science+Business Media; Volume: 13; Issue: 3 Linguagem: Inglês

10.1007/bf01799387

1573-2665

P. Divry, C. Vianey‐Liaud, C. Jakobs, H TENBRINK, J Dutruge, R Gilly,

Neonatal Health and Biochemistry

Journal of Inherited Metabolic DiseaseVolume 13, Issue 3 p. 330-332 Short Communication Sudden infant death syndrome: Organic acid profiles in cerebrospinal fluid from 47 children and the occurrence ofN-acetylaspartic acid P. Divry, P. Divry Unité d'Etude des Maladies Métaboliques, Hôpital Debrousse, Lyon Cédex 05, 69322 FranceSearch for more papers by this authorC. Vianey-Liaud, C. Vianey-Liaud Unité d'Etude des Maladies Métaboliques, Hôpital Debrousse, Lyon Cédex 05, 69322 FranceSearch for more papers by this authorC. Jakobs, C. Jakobs Department of Paediatrics, Free University Hospital, Amsterdam, 1007 MB The NetherlandsSearch for more papers by this authorH. J. Ten-Brink, H. J. Ten-Brink Department of Paediatrics, Free University Hospital, Amsterdam, 1007 MB The NetherlandsSearch for more papers by this authorJ. Dutruge, J. Dutruge Service de Pédiatrie, Centre Hospitalier Lyon Sud, Pierre Benite, 69310 FranceSearch for more papers by this authorR. Gilly, R. Gilly Service de Pédiatrie, Centre Hospitalier Lyon Sud, Pierre Benite, 69310 FranceSearch for more papers by this author P. Divry, P. Divry Unité d'Etude des Maladies Métaboliques, Hôpital Debrousse, Lyon Cédex 05, 69322 FranceSearch for more papers by this authorC. Vianey-Liaud, C. Vianey-Liaud Unité d'Etude des Maladies Métaboliques, Hôpital Debrousse, Lyon Cédex 05, 69322 FranceSearch for more papers by this authorC. Jakobs, C. Jakobs Department of Paediatrics, Free University Hospital, Amsterdam, 1007 MB The NetherlandsSearch for more papers by this authorH. J. Ten-Brink, H. J. Ten-Brink Department of Paediatrics, Free University Hospital, Amsterdam, 1007 MB The NetherlandsSearch for more papers by this authorJ. Dutruge, J. Dutruge Service de Pédiatrie, Centre Hospitalier Lyon Sud, Pierre Benite, 69310 FranceSearch for more papers by this authorR. Gilly, R. Gilly Service de Pédiatrie, Centre Hospitalier Lyon Sud, Pierre Benite, 69310 FranceSearch for more papers by this author First published: 01 May 1990 https://doi.org/10.1007/BF01799387Citations: 5AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1Divry P., Vianey-Liaud C., Cotte J. (1987) Routine gas chromatography/mass spectrometric analysis of urinary organic acids. Results over a three-year period. Biomed. Environ. Mass. Spectrom., 14: 663–668. 10.1002/bms.1200141117 CASPubMedWeb of Science®Google Scholar 2Divry P., Vianey-Liaud C., Gay C., Macabeo V., Rapin F., Echenne B. (1988) N-Acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophy. J. Inher. Metab. Dis., 11: 307–308. 10.1007/BF01800378 CASPubMedWeb of Science®Google Scholar 3Hagenfeldt L., Bollgren I., Venizelos N. (1987) N-Acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophy. J. Inher. Metab. Dis., 10: 135–141. 10.1007/BF01800038 CASPubMedWeb of Science®Google Scholar 4Kvittingen E. A., Guldal G., Borsting S., Skalpe I. O., Stokke O., Jellum E. (1986) N-Acetylaspartic aciduria in a child with a progressive cerebral atrophy. Clin. Chim. Acta, 158: 217–227. 10.1016/0009-8981(86)90285-8 CASPubMedWeb of Science®Google Scholar 5Matalon R., Kaul R., Casanova J., Michals K., Johnson A., Rapin I., Gashkoff P., Deanchin G. M. (1989) Aspartoacylase deficiency: the enzyme defect in Canavan disease. J. Inher. Metab. Dis, 12 (suppl. 2): 329–331. 10.1007/BF03335413 Google Scholar Citing Literature Volume13, Issue3May 1990Pages 330-332 ReferencesRelatedInformation