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• W1987876987 abstract "Journal of Inherited Metabolic DiseaseVolume 14, Issue 3 p. 325-328 Short Communication Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Different clinical expression in three unrelated patients R. J. A. Wanders, R. J. A. Wanders Department of Paediatrics, University Hospital, Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorL. Ijlst, L. Ijlst Department of Paediatrics, University Hospital, Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorM. Duran, M. Duran Department of Paediatrics, Free University Amsterdam, de Boelelaan 1117, Amsterdam, 1081 HV The NetherlandsSearch for more papers by this authorC. Jakobs, C. Jakobs Sophia Kinderziekenhuis, Gordelweg 160, Rotterdam, 3038 GE The NetherlandsSearch for more papers by this authorJ. B. C. de Klerk, J. B. C. de Klerk Sophia Kinderziekenhuis, Gordelweg 160, Rotterdam, 3038 GE The NetherlandsSearch for more papers by this authorH. Przyrembel, H. Przyrembel Sophia Kinderziekenhuis, Gordelweg 160, Rotterdam, 3038 GE The NetherlandsSearch for more papers by this authorF. Rocchiccioli, F. Rocchiccioli Saint Vincent de Paul Hospital, 82 Avenue Denfert Rochereau, Paris, FranceSearch for more papers by this authorP. Aubourg, P. Aubourg Saint Vincent de Paul Hospital, 82 Avenue Denfert Rochereau, Paris, FranceSearch for more papers by this author R. J. A. Wanders, R. J. A. Wanders Department of Paediatrics, University Hospital, Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorL. Ijlst, L. Ijlst Department of Paediatrics, University Hospital, Amsterdam, Meibergdreef 9, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorM. Duran, M. Duran Department of Paediatrics, Free University Amsterdam, de Boelelaan 1117, Amsterdam, 1081 HV The NetherlandsSearch for more papers by this authorC. Jakobs, C. Jakobs Sophia Kinderziekenhuis, Gordelweg 160, Rotterdam, 3038 GE The NetherlandsSearch for more papers by this authorJ. B. C. de Klerk, J. B. C. de Klerk Sophia Kinderziekenhuis, Gordelweg 160, Rotterdam, 3038 GE The NetherlandsSearch for more papers by this authorH. Przyrembel, H. Przyrembel Sophia Kinderziekenhuis, Gordelweg 160, Rotterdam, 3038 GE The NetherlandsSearch for more papers by this authorF. Rocchiccioli, F. Rocchiccioli Saint Vincent de Paul Hospital, 82 Avenue Denfert Rochereau, Paris, FranceSearch for more papers by this authorP. Aubourg, P. Aubourg Saint Vincent de Paul Hospital, 82 Avenue Denfert Rochereau, Paris, FranceSearch for more papers by this author First published: 01 May 1991 https://doi.org/10.1007/BF01811694Citations: 19AboutPDF 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 References 1Duran M., Wanders R. J. A., deJager J. P., Dorland L., Bruinvis L., Ketting D., Ijlst L., vanSprang F. J. (1991) 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacylcoenzyme A deficiency associated with sudden neonatal death. Protective effect of medium-chain triglyceride treatment. Eur. J. Pediatr., 150: 190– 195. 2Hale D. E., Thorpe C., Braat K., Wright J. H., Roe C. R., Coates P. M., Hashimoto T., Glasgow A. M., Tanaka K., Coates P. M. (1990) Thel-3-hydroxyacyl-CoA dehydrogenase deficiency. In: Fatty Acid Oxidation, New York: Alan R. Liss, 503– 510. 3Kelley R. I., Morton D. H. (1988) 3-Hydroxyoctanoic aciduria: identification of a new organic acid in the urine of a patient with non-ketotic hypoglycaemia. Clin. Chim. Acta, 175: 19– 26. 4Pollitt R. J., Tanaka K., Coates P. M. (1990) Clinical and biochemical presentation in 20 cases of hydroxydicarboxylic aciduria. In: Fatty Acid Oxidation, New York: Alan R. Liss, 495– 502. 5Pollitt R. J., Losty H., Westwood A. (1987) 3-Hydroxydicarboxylic aciduria: a distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance. J. Inher. Metab. Dis., 10 (Suppl. 2): 266– 269. 6Poll-The B. T., Bonnefont J. P., Ogier H., Charpentier C., Pelet A., LeFur J. M., Jakobs C., Kok R. M., Duran M., Divry P., Scotto J., Saudubray J. M. (1988) Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. J. Inher. Metab. Dis., 11 (Suppl. 2): 183– 185. 7Riudor E., Ribes A., Borowat M., Sabado C., Dominquez C., Ballabriga A. (1986) A new case of familiar C6–C14 dicarboxylic aciduria with favourable evolution. J. Inher. Metab. Dis., 9 (Suppl. 2): 297– 299. 8Wanders R. J. A., IJlst L., vanGennip A. H., Jakobs C., deJager J. P., Dorland L., vanSprang F. J., Duran M. (1990) Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acidβ-oxidation. J. Inher. Metab. Dis., 13: 311– 314. 9Wanders R. J. A., vanRoermund C. W. T., Schelen A., Schutgens R. B. H., Tager J. M., Stephenson J. B. P., Clayton P. T. (1990) A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomalβ-oxidation enzyme activities. J. Inher. Metab. Dis., 13: 375– 379. Citing Literature Volume14, Issue3May 1991Pages 325-328 ReferencesRelatedInformation" @default.
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