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Neurology|August 12, 2009
Decreased GABA-A binding on FMZ-PET in succinic semialdehyde dehydrogenase deficiencyP L Pearl, K M Gibson, Z Quezado, et al.Pediatric Research|June 1, 2000
2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolismK M Gibson, T G Burlingame, B Hogema, et al.Journal of Wound Care|June 11, 1999
Pressure sore prevention in hospital patients: a clinical auditP S Grewal, N H Sawant, C N Deaney, et al.Journal of Inherited Metabolic Disease|October 13, 2009
Development and implementation of a novel assay for L-2-hydroxyglutarate dehydrogenase (L-2-HGDH) in cell lysates: L-2-HGDH deficiency in 15 patients with L-2-hydroxyglutaric aciduriaM Kranendijk, G S Salomons, K M Gibson, et al.American Journal of Human Genetics|February 15, 2001
The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolismM E Gallardo, L R Desviat, J M Rodríguez, et al.Journal of Inherited Metabolic Disease|December 23, 2006
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiencyG S Salomons, C Jakobs, L Landegge Pope, et al.Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.Molecular Genetics and Metabolism|March 27, 2014
Phenylketonuria Scientific Review Conference: state of the science and future research needsKathryn M Camp, Melissa A Parisi, Phyllis B Acosta, et al.Pageof 25