Showing results (61-70 of 134) with videos related to

Sort By:
Pageof 14
Pediatrics|February 1, 1984
Parental response to repeat testing of infants with 'false-positive' results in a newborn screening programJ R Sorenson, H L Levy, T W Mangione, et al.
Human Mutation|January 4, 2001
Novel mutations in the GALK1 gene in patients with galactokinase deficiencyM Hunter, D Angelicheva, H L Levy, et al.
The American Journal of Medicine|June 1, 1976
Pericardial fluid analysis in scleroderma (systemic sclerosis)D D Gladman, D A Gordon, M B Urowitz, et al.
American Journal of Ophthalmology|June 1, 1984
Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalitiesR M Robb, S B Dowton, A B Fulton, et al.
The Journal of Pediatrics|December 1, 1996
Vitreous hemorrhage as an ophthalmic complication of galactosemiaH L Levy, A E Brown, S E Williams, et al.
American Journal of Obstetrics and Gynecology|September 16, 1999
Maternal gamma-cystathionase deficiency: absence of both teratogenic effects and pregnancy complicationsJ E Vargas, S H Mudd, S E Waisbren, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 6, 1975
Cystathioninuria and homocystinuriaH L Levy, S H Mudd, B W Uhlendorf, et al.
Pediatrics|March 1, 1985
Cerebrospinal fluid neurotransmitter metabolites in neurologically normal infants and childrenP J Langlais, F X Walsh, E D Bird, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Review of neuropsychological functioning in treated phenylketonuria: an information processing approachS E Waisbren, M J Brown, L M de Sonneville, et al.
American Journal of Human Genetics|November 1, 1981
A study of cardiovascular risk in heterozygotes for homocystinuriaS H Mudd, R Havlik, H L Levy, et al.
Pageof 14