L-2-Hydroxyglutarazidurie: Eine neue Enzephalopathie mit leukodystrophen Veränderungen
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-93411-7_22.pdf
Reference4 articles.
1. Duran M, Kamerling JP, Bakker HD, van Gennip AH, Wadman SK (1980) L-2-Hydroxyglutaric aciduria: An inborn error of metabolism. J Inher Metab Dis 3: 109–112
2. Jaeken J, Willekens H, Corbeel L (1988) Leukodystrophy associated with hyperlysinorhachia and 2-hydroxyglutaric aciduria. Ped Res 24: 266
3. Hoffmann G, Aramaki S, Blum-Hoffmann E, Nyhan WL, Sweetman L (1989) Quantitative analysis for organic acids in biological samples: Batch isolation followed by gas chromatographic-mass spectrometric analysis. Clin Chem 35: 587–595
4. Shuman RM, Leech RW, Scott CR (1978) The neuropathology of the nonketotic and ketotic hyperglycinemias: Three cases. Neurology 28: 139–146
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. l-2-Hydroxyglutaric acidaemia: Clinical and biochemical findings in 12 patients and preliminary report onl-2-hydroxyacid dehydrogenase;Journal of Inherited Metabolic Disease;1993
2. Physiology and pathophysiology of organic acids in cerebrospinal fluid;Journal of Inherited Metabolic Disease;1993
3. L-2-hydroxyglutaric acidemia: A novel inherited neurometabolic disease;Annals of Neurology;1992-07
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