Showing results (701-710 of 1,345) with videos related to
Sort By:
Pageof 135
Pediatric Neurosurgery|April 15, 1999
Intraoperative angiography in the management of pediatric vascular disordersS Ghosh, M L Levy, P Stanley, et al.Psychopharmacologia|October 31, 1975
Smooth-pursuit eye movements, and diazepam, CPZ, and secobarbitalP S Holzman, D L Levy, E H Uhlenhuth, et al.Molecular Genetics and Metabolism Reports|January 9, 2019
Untargeted metabolomics identifies unique though benign biochemical changes in patients with pathogenic variants in UROC1Kevin E Glinton, Harvey L Levy, Adam D Kennedy, et al.BMC Genetics|July 31, 2001
A missense mutation (Q279R) in the fumarylacetoacetate hydrolase gene, responsible for hereditary tyrosinemia, acts as a splicing mutationN Dreumont, J A Poudrier, A Bergeron, et al.The Journal of Reproductive Medicine|December 25, 2002
Effect of labor induction on cesarean section rates in diabetic pregnanciesAnna L Levy, Jose L Gonzalez, Valerie J Rappaport, et al.The Journal of Pediatrics|September 20, 2001
Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acidsL R Kalsner, F J Rohr, K A Strauss, et al.American Journal of Public Health|December 1, 1995
Psychosocial factors in maternal phenylketonuria: women's adherence to medical recommendationsS E Waisbren, B D Hamilton, P J St James, et al.Neurology|January 1, 1978
Vitamin B6-dependent seizures: pathology and chemical findings in brainI T Lott, T Coulombe, R V Di Paolo, et al.Pediatric Research|March 1, 1984
Congenital expression of prolidase defect in prolidase deficiencyE R Naughten, S P Proctor, H L Levy, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.Pageof 135