S. Grünewald

Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment.

M. Baumgartner, D. Rizopoulos, Y. Chien, 2019, Molecular genetics and metabolism.

Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres

M. Baumgartner, O. Bodamer, E. Morava, 2008, Journal of Inherited Metabolic Disease.

Neonatal lethal mitochondrial trifunctional protein deficiency mimicking a respiratory chain defect

R. Wanders, U. Wendel, J. Bakkeren, 1997, Journal of Inherited Metabolic Disease.

Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters

M. Baumgartner, O. Bodamer, E. Morava, 2009, Journal of Inherited Metabolic Disease.