M S Korson

Urinary lactate excretion to monitor the efficacy of treatment of type I glycogen storage disease.

J. Wolfsdorf, J I Wolfsdorf, T Hagen, 2000, Molecular genetics and metabolism.

Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disorders.

J L Merritt, B F Scharschmidt, S. Cederbaum, 2012, Molecular genetics and metabolism.

Clinical approach to genetic cardiomyopathy in children.

S. Lipshultz, A. Lin, A. Perez-Atayde, 1996, Circulation.

Perioperative white matter degeneration and death in a patient with a defect in mitochondrial oxidative phosphorylation.

A. Casta, C. Houck, M S Korson, 1997, Anesthesiology.