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Sensitivity and specificity of free and total glutaric acid and 3-hydroxyglutaric acid measurements by stable-isotope dilution assays for the diagnosis of glutaric aciduria type I.
J Inherit Metab Dis. 1999 Dec;22(8):867-81. doi: 10.1023/a:1005683222187.
J Inherit Metab Dis. 1999.
PMID: 10604139
Clinical Trial.
Biochemistry of glutaric aciduria type I: activities of in vitro expressed wild-type and mutant cDNA encoding human glutaryl-CoA dehydrogenase.
Liesert M, Zschocke J, Hoffmann GF, Mühlhäuser N, Buckel W.
Liesert M, et al.
J Inherit Metab Dis. 1999 May;22(3):256-8. doi: 10.1023/a:1005525903207.
J Inherit Metab Dis. 1999.
PMID: 10384381
No abstract available.
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Formation of 3-hydroxyglutaric acid in glutaric aciduria type I: in vitro participation of medium chain acyl-CoA dehydrogenase.
Peters V, Morath M, Mack M, Liesert M, Buckel W, Hoffmann GF, Vockley J, Ghisla S, Zschocke J.
Peters V, et al. Among authors: liesert m.
JIMD Rep. 2019 Mar 26;47(1):30-34. doi: 10.1002/jmd2.12026. eCollection 2019 May.
JIMD Rep. 2019.
PMID: 31240164
Free PMC article.
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Mutations in the AUH gene cause 3-methylglutaconic aciduria type I.
Ly TB, Peters V, Gibson KM, Liesert M, Buckel W, Wilcken B, Carpenter K, Ensenauer R, Hoffmann GF, Mack M, Zschocke J.
Ly TB, et al. Among authors: liesert m.
Hum Mutat. 2003 Apr;21(4):401-7. doi: 10.1002/humu.10202.
Hum Mutat. 2003.
PMID: 12655555
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Biochemical characterization of human 3-methylglutaconyl-CoA hydratase and its role in leucine metabolism.
Mack M, Schniegler-Mattox U, Peters V, Hoffmann GF, Liesert M, Buckel W, Zschocke J.
Mack M, et al. Among authors: liesert m.
FEBS J. 2006 May;273(9):2012-22. doi: 10.1111/j.1742-4658.2006.05218.x.
FEBS J. 2006.
PMID: 16640564
Free article.
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3-Methylglutaconyl-CoA hydratase from Acinetobacter sp.
Mack M, Liesert M, Zschocke J, Peters V, Linder D, Buckel W.
Mack M, et al. Among authors: liesert m.
Arch Microbiol. 2006 May;185(4):297-306. doi: 10.1007/s00203-006-0095-7. Epub 2006 Feb 16.
Arch Microbiol. 2006.
PMID: 16482430
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