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Uta Lichter-Konecki

Showing results (1-10 of 56) with videos related to

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Drugs|March 14, 2019
Phenylketonuria: Current Treatments and Future DevelopmentsUta Lichter-Konecki, Jerry Vockley
Pediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism with Cognitive Impairment: Metabolism Defects of Phenylalanine, Homocysteine and Methionine, Purine and Pyrimidine, and CreatineEvgenia Sklirou, Uta Lichter-Konecki
Paediatric Drugs|September 21, 2025
Current Treatment Modalities for Urea Cycle DisordersNicholas Ah Mew, Uta Lichter-Konecki
Molecular Genetics and Metabolism Reports|March 26, 2016
Phenylketonuria (PKU): A problem solved?Christine S Brown, Uta Lichter-Konecki
Pediatric Research|July 15, 2023
Relationship between longitudinal changes in neuropsychological outcome and disease biomarkers in urea cycle disordersUta Lichter-Konecki, Jacqueline H Sanz, , et al.
The Journal of Pediatrics|September 3, 2013
Genomics in newborn screeningYuval E Landau, Uta Lichter-Konecki, Harvey L Levy
Molecular Genetics and Metabolism|September 23, 2011
Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficienciesNenad Blau, Julia B Hennermann, Ulrich Langenbeck, et al.
JIMD Reports|February 19, 2015
Severe neonatal holocarboxylase synthetase deficiency in west african siblingsMauricio De Castro, Dina J Zand, Uta Lichter-Konecki, et al.
Molecular Genetics and Metabolism|December 3, 2014
What is in the can? The dilemma with dietary supplementsKristin D'Aco, Robert Mooney, Kristina Cusmano-Ozog, et al.
Glia|January 11, 2008
Gene expression profiling of astrocytes from hyperammonemic mice reveals altered pathways for water and potassium homeostasis in vivoUta Lichter-Konecki, Jean Marie Mangin, Heather Gordish-Dressman, et al.
Pageof 6

Showing results (1-10 of 56) with videos related to

Sort By:
Pageof 6
Drugs|March 14, 2019
Phenylketonuria: Current Treatments and Future DevelopmentsUta Lichter-Konecki, Jerry Vockley
Pediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism with Cognitive Impairment: Metabolism Defects of Phenylalanine, Homocysteine and Methionine, Purine and Pyrimidine, and CreatineEvgenia Sklirou, Uta Lichter-Konecki
Paediatric Drugs|September 21, 2025
Current Treatment Modalities for Urea Cycle DisordersNicholas Ah Mew, Uta Lichter-Konecki
Molecular Genetics and Metabolism Reports|March 26, 2016
Phenylketonuria (PKU): A problem solved?Christine S Brown, Uta Lichter-Konecki
Pediatric Research|July 15, 2023
Relationship between longitudinal changes in neuropsychological outcome and disease biomarkers in urea cycle disordersUta Lichter-Konecki, Jacqueline H Sanz, , et al.
The Journal of Pediatrics|September 3, 2013
Genomics in newborn screeningYuval E Landau, Uta Lichter-Konecki, Harvey L Levy
Molecular Genetics and Metabolism|September 23, 2011
Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficienciesNenad Blau, Julia B Hennermann, Ulrich Langenbeck, et al.
JIMD Reports|February 19, 2015
Severe neonatal holocarboxylase synthetase deficiency in west african siblingsMauricio De Castro, Dina J Zand, Uta Lichter-Konecki, et al.
Molecular Genetics and Metabolism|December 3, 2014
What is in the can? The dilemma with dietary supplementsKristin D'Aco, Robert Mooney, Kristina Cusmano-Ozog, et al.
Glia|January 11, 2008
Gene expression profiling of astrocytes from hyperammonemic mice reveals altered pathways for water and potassium homeostasis in vivoUta Lichter-Konecki, Jean Marie Mangin, Heather Gordish-Dressman, et al.
Pageof 6