Showing results (81-90 of 134) with videos related to
Sort By:
Pageof 14
JAMA|June 2, 1978
Screening for congenital hypothyroidism. Results in the newborn population of New EnglandM L Mitchell, P R Larsen, H L Levy, et al.Metabolism: Clinical and Experimental|January 6, 2001
Isolated hypermethioninemia: measurements of S-adenosylmethionine and cholineS H Mudd, D J Jenden, A Capdevila, et al.The New England Journal of Medicine|May 26, 1983
Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemiaM K Hostetter, H L Levy, H S Winter, et al.American Journal of Public Health|July 1, 1988
The New England Maternal PKU Project: identification of at-risk womenS E Waisbren, L B Doherty, I V Bailey, 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 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 14