2-methylacetoacetyl-coenzyme A thiolase (beta-ketothiolase) deficiency: one disease - two pathways by Sarah C. Grünert, Jörn Oliver Sass

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Correction to: 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces by Sarah C. Grünert, Jörn Oliver Sass

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Beta-ketothiolase deficiency: An unusual cause of recurrent ketoacidosis by Gonca Kılıç-Yıldırım, Sultan Durmuş-Aydoğdu, Serdar Ceylaner, Jörn Oliver Sass

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Amino Acids and Inherited Amino Acid-Related Disorders by Ina Knerr, Laurie Bernstein, Ellen Crushell, Siobhan O’Sullivan, Jörn Oliver Sass

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The glycine N-acyltransferases, GLYAT and GLYATL1, contribute to the detoxification of isovaleryl-CoA - an in-silico and in vitro validation by Stefan Kühn, Monray E. Williams, Marli Dercksen, Jörn Oliver Sass, Rencia van der Sluis

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Mimicking Ketonuria in the Ketogenesis Defect 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency by Jörn Oliver Sass Dr. rer. nat., Malkanthi Fernando Dr. rer. nat., Sidney Behringer B.Sc.

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Inborn Errors of Ketone Body Metabolism and Transport by Jörn Oliver Sass Dr. rer. nat., Toshiyuki Fukao MD, PhD, Grant A. Mitchell MD

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Amino acids regulate transgene expression in MDCK cells. by Marta Torrente, Adriano Guetg, Jörn Oliver Sass, Lisa Arps, Lisa Ruckstuhl, Simone M R Camargo, François Verrey

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