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Molecular Genetics and Metabolism Reports|July 10, 2024
Long-term use of investigational β-Hydroxybutyrate salts in children with multiple acyl-CoA dehydrogenase or pyruvate dehydrogenase deficiencyAndrew A M Morris, Bernard Cuenoud, Philippe Delerive, et al.JIMD Reports|September 26, 2015
Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyP Bala, S Ferdinandusse, S E Olpin, et al.Journal of Occupational Medicine. : Official Publication of the Industrial Medical Association|December 1, 1992
The P300 event-related potential. The effects of sleep deprivationA M Morris, Y So, K A Lee, et al.Pediatric Nephrology (Berlin, Germany)|December 3, 2008
Peritoneal dialysis for chronic renal failure in a patient with methylmalonic acidaemiaBemigho Etuwewe, Caroline A Jones, Shipra Mathur, et al.Atherosclerosis|April 27, 2000
360His polymorphism of the apolipoproteinA-IV gene and plasma lipid response to energy restricted diets in overweight subjectsL K Heilbronn, M Noakes, A M Morris, et al.Developmental Pharmacology and Therapeutics|January 1, 1984
Arginine vasopressin metabolic clearance and production rates in fetal sheep, pregnant ewes, and lambsH Stegner, R D Leake, S M Palmer, et al.Neuropediatrics|August 26, 2004
Biotinidase deficiency: a treatable leukoencephalopathyS Grünewald, M P Champion, J V Leonard, et al.Annals of Clinical and Laboratory Science|July 1, 1976
Chronic toxic nephropathies--diagnosis and managementP Balter, R C Muehrcke, A M Morris, et al.Journal of Inherited Metabolic Disease|September 16, 2003
What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?A M Lund, M A Dixon, P Vreken, et al.Journal of Inherited Metabolic Disease|September 16, 2003
Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, M A Dixon, P Vreken, et al.Pageof 12