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Julia B Hennermann

Showing results (1-10 of 97) with videos related to

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MMW Fortschritte Der Medizin|February 16, 2026
[Alpha-mannosidosis]Julia B Hennermann
Journal of Inherited Metabolic Disease|September 18, 2013
Unknown pathomechanisms of renal impairment in PKUJulia B Hennermann, Uwe Querfeld
Journal of Inherited Metabolic Disease|April 29, 2015
Jürgen HerwigAdrian C Sewell, Julia B Hennermann
Deutsche Medizinische Wochenschrift (1946)|October 9, 2024
[Lysosomal storage disorders - Fabry disease and Gaucher disease]Lucia Segura Schmitz, Julia B Hennermann, André Lollert
Molecular Genetics and Metabolism Reports|March 18, 2021
Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screeningGwendolyn Gramer, Georg F Hoffmann, Julia B Hennermann
Journal of Perinatal Medicine|September 7, 2004
Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuriaJulia B Hennermann, Andrea Loui, Astrid Weber, et al.
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.
Molecular Genetics and Metabolism|July 30, 2005
Long-term treatment with tetrahydrobiopterin increases phenylalanine tolerance in children with severe phenotype of phenylketonuriaJulia B Hennermann, Christoph Bührer, Nenad Blau, et al.
Journal of Inherited Metabolic Disease|December 25, 2009
False-positive newborn screening mimicking glutaric aciduria type I in infants with renal insufficiencyJulia B Hennermann, Sylvia Roloff, Jutta Gellermann, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 12, 2021
Retinal thinning in phenylketonuria and Gaucher disease type 3Susanne Hopf, Alexander K Schuster, Julia B Hennermann, et al.
Pageof 10

Showing results (1-10 of 97) with videos related to

Sort By:
Pageof 10
MMW Fortschritte Der Medizin|February 16, 2026
[Alpha-mannosidosis]Julia B Hennermann
Journal of Inherited Metabolic Disease|September 18, 2013
Unknown pathomechanisms of renal impairment in PKUJulia B Hennermann, Uwe Querfeld
Journal of Inherited Metabolic Disease|April 29, 2015
Jürgen HerwigAdrian C Sewell, Julia B Hennermann
Deutsche Medizinische Wochenschrift (1946)|October 9, 2024
[Lysosomal storage disorders - Fabry disease and Gaucher disease]Lucia Segura Schmitz, Julia B Hennermann, André Lollert
Molecular Genetics and Metabolism Reports|March 18, 2021
Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screeningGwendolyn Gramer, Georg F Hoffmann, Julia B Hennermann
Journal of Perinatal Medicine|September 7, 2004
Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuriaJulia B Hennermann, Andrea Loui, Astrid Weber, et al.
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.
Molecular Genetics and Metabolism|July 30, 2005
Long-term treatment with tetrahydrobiopterin increases phenylalanine tolerance in children with severe phenotype of phenylketonuriaJulia B Hennermann, Christoph Bührer, Nenad Blau, et al.
Journal of Inherited Metabolic Disease|December 25, 2009
False-positive newborn screening mimicking glutaric aciduria type I in infants with renal insufficiencyJulia B Hennermann, Sylvia Roloff, Jutta Gellermann, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 12, 2021
Retinal thinning in phenylketonuria and Gaucher disease type 3Susanne Hopf, Alexander K Schuster, Julia B Hennermann, et al.
Pageof 10