<scp>l</scp>‐2‐Hydroxyglutaric aciduria: Two further cases

L‐2‐Hydroxyglutaric aciduria: an inborn error of metabolism?

M. Durán, J.P. Kamerling, H. D. Bakker et al. · Journal of Inherited Metabolic Disease · 1980 · 221 citations

Life Sciences, Biochemistry, Cellular Metabolism +7

<scp>L</scp>‐2‐hydroxyglutaric acidemia: A novel inherited neurometabolic disease

P. G. Barth, Georg F. Hoffmann, J. Jaeken et al. · Annals of Neurology · 1992 · 151 citations

Life Sciences, Biochemistry, Neurology +15

D‐2‐hydroxyglutaric aciduria: Case report and biochemical studies

R. A. Chalmers, A. M. Lawson, R. W. E. Watts et al. · Journal of Inherited Metabolic Disease · 1980 · 132 citations

Medicine, Biochemistry, Pathology +10

<scp>d</scp>‐2‐Hydroxyglutaric aciduria in a newborn with neurological abnormalities: A new neurometabolic disorder?

K. Michael Gibson, William Craigen, Gail E. Herman et al. · Journal of Inherited Metabolic Disease · 1993 · 45 citations

Medicine, Neurology, Pediatrics +13

Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period

P. Divry, C. Vianey‐Liaud, J Cotte · Journal of Mass Spectrometry · 1987 · 28 citations

Life Sciences, Biochemistry, Chromatographic Analysis +14