L-2-hydroxyglutaric acidemia: A novel inherited neurometabolic disease-Reference-Cited by-同舟云学术

L-2-hydroxyglutaric acidemia: A novel inherited neurometabolic disease

Published:1992-07 Issue:1 Volume:32 Page:66-71
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Barth Peter G.,Hoffmann Georg F.,Jaeken Jaak,Lehnert Willy,Hanefeld Folker,Van Gennip Albert H.,Duran Marinus,Valk Jaap,Schutgens Ruud B. H.,Trefz Friedrich K.,Reimann Gabriele,Hartung Hans-Peter

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference11 articles.

1. L-2-Hydroxyglutaric aciduria: an inborn error of metabolism?

2. 34 LEUKODYSTROPHY ASSOCIATED WITH HYPERLYSINORHACHIA AND 2-HYDROXYGLUTARIC ACIDURIA

3. et al. L-2-Hydroxyglutarazidurie: Eine neue Enzephalopathie mit leukodystrophen Veränderungen. In: eds. Aktuelle Neuropädiatrie 1989. New York: Springer, 1990: 139-142

4. Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometry

5. Quantitative analysis for organic acids in biological samples: batch isolation followed by gas chromatographic-mass spectrometric analysis.

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