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W B Hanley

Showing results (31-40 of 38) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The international collaborative study of maternal phenylketonuria: status report 1994R Koch, H L Levy, R Matalon, et al.
The Journal of Clinical Investigation|February 1, 1984
Biopterin synthesis defect. Treatment with L-dopa and 5-hydroxytryptophan compared with therapy with a tetrahydropterinR R McInnes, S Kaufman, J J Warsh, et al.
European Journal of Pediatrics|July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemiaH L Levy, S E Waisbren, D Lobbregt, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case findingW B Hanley, L D Platt, R P Bachman, 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.
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.
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.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The international collaborative study of maternal phenylketonuria: status report 1994R Koch, H L Levy, R Matalon, et al.
The Journal of Clinical Investigation|February 1, 1984
Biopterin synthesis defect. Treatment with L-dopa and 5-hydroxytryptophan compared with therapy with a tetrahydropterinR R McInnes, S Kaufman, J J Warsh, et al.
European Journal of Pediatrics|July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemiaH L Levy, S E Waisbren, D Lobbregt, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case findingW B Hanley, L D Platt, R P Bachman, 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.
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.
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.
Pageof 4