Hydroxylysine

glutaryl-CoA dehydrogenase ; Homo sapiens







14 Article(s)
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1 33423247 [Expert consensus for the diagnosis and treatment of glutaricacidemia type 1]. 2021 Jan 10 1
2 31491587 Potential complementation effects of two disease-associated mutations in tetrameric glutaryl-CoA dehydrogenase is due to inter subunit stability-activity counterbalance. 2020 Jan 3
3 32306145 Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder. 2020 Jul 1
4 28411331 Glutaric Acidemia Type 1: A Case of Infantile Stroke. 2018 2
5 29292490 Two Uneventful Pregnancies in a Woman with Glutaric Aciduria Type 1. 2018 1
6 26656312 Clinical and molecular investigation in Chinese patients with glutaric aciduria type I. 2016 Jan 30 1
7 24587932 A treatable neurometabolic disorder: glutaric aciduria type 1. 2014 1
8 21431622 Diagnosis and management of glutaric aciduria type I--revised recommendations. 2011 Jun 1
9 17879145 Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency. 2007 Oct 2
10 16602100 Glutaric acidemia type 1. 2006 May 15 1
11 15351027 Glutaric aciduria type 1: proton magnetic resonance spectroscopy findings. 2004 Sep 1
12 15505399 Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: anticholinergic drugs and botulinum toxin as additional therapeutic options. 2004 1
13 10985795 Proton abstraction reaction, steady-state kinetics, and oxidation-reduction potential of human glutaryl-CoA dehydrogenase. 2000 Sep 19 1
14 9600243 The human glutaryl-CoA dehydrogenase gene: report of intronic sequences and of 13 novel mutations causing glutaric aciduria type I. 1998 Apr 1