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5 in total

1. Glutaric aciduria: inherited deficiency of glutaryl-CoA dehydrogenase activity.

Authors: S I Goodman; J G Kohlhoff
Journal: Biochem Med Date: 1975-06

2. Hypothesis: a role for quinolinic acid in the neuropathology of glutaric aciduria type I.

Authors: M P Heyes
Journal: Can J Neurol Sci Date: 1987-08 Impact factor: 2.104

3. Inhibition of brain glutamate decarboxylase by glutarate, glutaconate, and beta-hydroxyglutarate: explanation of the symptoms in glutaric aciduria?

Authors: O Stokke; S I Goodman; P G Moe
Journal: Clin Chim Acta Date: 1976-02-02 Impact factor: 3.786

4. Artifactual increases in the concentration of free GABA in samples of human cerebrospinal fluid are due to degradation of homocarnosine.

Authors: J Grove; P J Schechter; G Tell; L Rumbach; C Marescaux; J M Warter; J Koch-Weser
Journal: J Neurochem Date: 1982-10 Impact factor: 5.372

5. Glutaric aciduria: biochemical and morphologic considerations.

Authors: S I Goodman; M D Norenberg; R H Shikes; D J Breslich; P G Moe
Journal: J Pediatr Date: 1977-05 Impact factor: 4.406

5 in total

2 in total

Review 1. Maintenance treatment of glutaryl-CoA dehydrogenase deficiency.

Authors: C Mühlhausen; G F Hoffmann; K A Strauss; S Kölker; J G Okun; C R Greenberg; E R Naughten; K Ullrich
Journal: J Inherit Metab Dis Date: 2004 Impact factor: 4.982

2. Macrocephaly, dystonia, and bilateral temporal arachnoid cysts: glutaric aciduria type 1.

Authors: J F Martínez-Lage; C Casas; M A Fernández; A Puche; T Rodriguez Costa; M Poza
Journal: Childs Nerv Syst Date: 1994-04 Impact factor: 1.475

2 in total