Showing results (121-130 of 134) with videos related to
Sort By:
Pageof 14
Journal of Inherited Metabolic Disease|March 21, 1998
Neonatal neurological assessment of offspring in maternal phenylketonuriaS E Waisbren, P Chang, H L Levy, et al.American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.American Journal of Human Genetics|July 1, 1996
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative StudyP Guldberg, H L Levy, W B Hanley, et al.JIMD Reports|November 6, 2013
Newborn Screening for Glutaric Aciduria-II: The New England ExperienceI Sahai, C L Garganta, J Bailey, et al.Pediatrics|August 3, 1999
Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative StudyF Güttler, C Azen, P Guldberg, et al.Lancet (London, England)|December 10, 1994
Maternal mild hyperphenylalaninaemia: an international survey of offspring outcomeH L Levy, S E Waisbren, D Lobbregt, et al.The Journal of Investigative Dermatology|November 6, 1998
Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemiaS G Khan, H L Levy, R Legerski, et al.American Journal of Obstetrics and Gynecology|February 29, 2000
The international study of pregnancy outcome in women with maternal phenylketonuria: report of a 12-year studyL D Platt, R Koch, W B Hanley, et al.Pediatric Research|May 1, 2001
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative StudyH L Levy, P Guldberg, F Güttler, et al.Journal of Inherited Metabolic Disease|February 24, 2001
Hepatocellular carcinoma despite long-term survival in chronic tyrosinaemia IS Z Kim, K G Kupke, L Ierardi-Curto, et al.Pageof 14