J. Inherit. Melab. Dis. 27 (2004) 921-926

"Looking forward- An evidence based approach to glutaryl-dehyrdogense deficiency."

J. Inherit. Melab. Dis. 27 (2004) 903-910

"Reduction of lysine intake while avoiding malnutrition- Major goals and major problems in dietary treatment of glutaryl-CoA dehyrdogense deficiency."

J. Inherit. Melab. Dis. 27 (2004) 893-902

"Emergency Treatment in glutaryl-coA dehydrogense deficiency."

J. Inherit. Melab. Dis. 27 (2004) 843-849

"Challenges for basic research in glutaryl-coA dehydrogense deficiency."

J. Inherit. Melab. Dis. 27 (2004) 805-812

"Excitotoxicity and biogenetics in glutaryl-coA dehydrogense deficiency."

"Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management."

"Segregation of human neural stem cells in the developing primate forebrain."

"Why screen neonates for glutaric aciduria?"

"Glutaric Aciduria Type 1: Prospective treatment of the Amish variant 1990-1998."

Pediatrics

"Through my window- remarks of the 125th year celebration of Children's Hospital of Boson."

American Journal of Medical Genetics

"Type 1 glutaric aciduris, part 2: A model of acute striatal necrosis."

Journal of Rare Diseases

"Clinical treatment guide to inborn errors of the metabolism, 1995."

Research article

"Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type 1."

Brain Advance Access<> Published 2007

"Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogense deficiency."