S. Kölker

Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I)

S. Kölker, E. Christensen, James V. Leonard et al. · Journal of Inherited Metabolic Disease · 2007 · 145 citations

Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency

Sonja Külkens, Inga Harting, Susanne K. Sauer et al. · Neurology · 2005 · 101 citations

Neurodegenerative Diseases, Glutaryl-coa Dehydrogenase, Corticobasal Degeneration +15

Glutaryl-CoA Dehydrogenase Deficiency: Region-Specific Analysis of Organic Acids and Acylcarnitines in<i>post mortem</i>Brain Predicts Vulnerability of the Putamen

S. Kölker, Georg F. Hoffmann, D. S. M. Schor et al. · Neuropediatrics · 2003 · 54 citations

Glucocorticoid, Glutaryl-coa Dehydrogenase Deficiency, Social Sciences +19

Late-onset multiple acyl-CoA dehydrogenase deficiency: A frequently missed diagnosis?

Sjaan Koppel, Jochen Gottschalk, Georg F. Hoffmann et al. · Neurology · 2006 · 13 citations

Metabolic Disorder, Genetics, Pathology +24