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The Journal of Pediatrics|June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, S M Willi, P Rinaldo, et al.
American Journal of Medical Genetics. Supplement|January 1, 1988
Therapeutic modification of membrane lipid abnormalities in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, G P Hosking, R Gayton, et al.
The Plant Journal : for Cell and Molecular Biology|March 22, 2001
Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1G Parry, A Delbarre, A Marchant, et al.
Annals of Emergency Medicine|August 25, 1999
Hypoketotic hypoglycemic coma in a 21-month-old childM A Hostetler, G L Arnold, R Mooney, et al.
JIMD Reports|February 23, 2013
Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA DeficiencyA A M Morris, S E Olpin, M J Bennett, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 5, 1982
Radioimmunoassay of thyroxine and 3,3',5'-triiodothyronine (reverse T3) in human amniotic fluidE Cooper, A Anderson, M J Bennett, et al.
Anesthesiology|September 1, 1976
Interaction of anesthesia, beta-receptor blockade, and blood loss in dogs with induced myocardial infarctionC Prys-Roberts, J G Roberts, P Foëx, et al.
Molecular Genetics and Metabolism|June 30, 2000
A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II geneG D Vladutiu, M J Bennett, D Smail, et al.
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