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Clinical Pharmacology and Therapeutics|November 20, 2016
Aberrant mTOR signaling and disrupted autophagy: The missing link in potential vigabatrin-associated ocular toxicity?K R Vogel, G R Ainslie, P L Pearl, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2018
Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuriaNicola Longo, David Dimmock, Harvey Levy, et al.
Molecular Genetics and Metabolism|September 16, 2018
Pharmacokinetics of glycerol phenylbutyrate in pediatric patients 2 months to 2 years of age with urea cycle disordersSusan A Berry, Jerry Vockley, Alexander A Vinks, et al.
Pediatric Neurology|March 1, 1993
Multiple syndromes of 3-methylglutaconic aciduriaK M Gibson, O N Elpeleg, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Pre- and postnatal diagnosis of succinic semialdehyde dehydrogenase deficiency using enzyme and metabolite assaysK M Gibson, C Baumann, H Ogier, et al.
Journal of Quality in Clinical Practice|September 1, 1994
A survey of persisting leg and/or foot pain in vascular surgery patientsK M Gibson, P A Jagiello, J J Tapper, et al.
European Journal of Pediatrics|September 1, 1984
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyW G Wilson, M B Cass, O Søvik, et al.
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