Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1

The metabolic and molecular bases of inherited disease

Ying-Tsong Chen · Medical Entomology and Zoology · 2001 · 6.9K citations

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Type I glutaric aciduria, part 1: Natural history of 77 patients

Kevin A. Strauss, Erik G. Puffenberger, D. Holmes Morton · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2003 · 322 citations

Medicine, Neurology, Pediatrics +13

Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency

Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg et al. · Pediatric Research · 2006 · 271 citations · Full text

Medicine, Child Health, Pediatrics +3

Sympathetic Innervation of Lymphoreticular Organs Is Rate Limiting for Prion Neuroinvasion

Markus Glatzel, Frank L. Heppner, Kathryn M. Albers et al. · Neuron · 2001 · 229 citations · Full text

Life Sciences, Infectious Diseases, Neuroscience +14

Intracerebral accumulation of glutaric and 3‐hydroxyglutaric acids secondary to limited flux across the blood–brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl‐CoA dehydrogenase deficiency

Sven W. Sauer, Jürgen G. Okun, Gert Fricker et al. · Journal of Neurochemistry · 2006 · 165 citations

Life Sciences, Biochemistry, Neuroscience +12