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Molecular Genetics and Metabolism|July 12, 2015
Metabolite studies in HIBCH and ECHS1 defects: Implications for screeningHeidi Peters, Sacha Ferdinandusse, Jos P Ruiter, et al.Journal of Inherited Metabolic Disease|December 23, 2011
Inhibition of 3-methylcrotonyl-CoA carboxylase explains the increased excretion of 3-hydroxyisovaleric acid in valproate-treated patientsPaula B M Luís, Jos P Ruiter, Lodewijk IJlst, et al.Biochemical Pharmacology|August 17, 2011
Valproic acid utilizes the isoleucine breakdown pathway for its complete β-oxidationPaula B M Luís, Jos P Ruiter, Rob Ofman, et al.Metabolism: Clinical and Experimental|January 3, 2012
Characterization of D-3-hydroxybutyrylcarnitine (ketocarnitine): an identified ketosis-induced metaboliteMaarten R Soeters, Mireille J Serlie, Hans P Sauerwein, et al.Molecular Genetics and Metabolism|November 25, 2018
Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorderChristos Chinopoulos, Spyros Batzios, Lambertus P van den Heuvel, et al.Pageof 1