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F Trefz

Showing results (11-20 of 27) with videos related to

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European Journal of Pediatrics|July 1, 1996
The International Collaborative Study on maternal phenylketonuria: organization, study design and description of the sampleE G Friedman, R Koch, C Azen, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'W B Hanley, C Azen, R Koch, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Patient's thoughts and expectations about centres of expertise for PKUA M J van Wegberg, A MacDonald, D Abeln, et al.
Molecular Genetics and Metabolism|September 26, 2000
Maternal phenylketonuria: an international studyR Koch, W Hanley, H Levy, et al.
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.
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.
Orphanet Journal of Rare Diseases|July 24, 2019
Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims dataK F Trefz, A C Muntau, K M Kohlscheen, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
European Journal of Pediatrics|July 1, 1996
The International Collaborative Study on maternal phenylketonuria: organization, study design and description of the sampleE G Friedman, R Koch, C Azen, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'W B Hanley, C Azen, R Koch, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Patient's thoughts and expectations about centres of expertise for PKUA M J van Wegberg, A MacDonald, D Abeln, et al.
Molecular Genetics and Metabolism|September 26, 2000
Maternal phenylketonuria: an international studyR Koch, W Hanley, H Levy, et al.
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.
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.
Orphanet Journal of Rare Diseases|July 24, 2019
Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims dataK F Trefz, A C Muntau, K M Kohlscheen, et al.
Pageof 3