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Georg F Hoffmann

Showing results (121-130 of 381) with videos related to

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BMC Medical Education|November 28, 2024
A novel blended and interprofessional approach to pediatric emergency training: self-assessment, perception, and perceived long-term effectsRonny Lehmann, Michaela Klinke Petrowsky, Anke Seitz, et al.
JIMD Reports|May 6, 2015
Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn ScreeningGwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 7, 2010
Expression and function of matrix Gla protein in human peritoneal mesothelial cellsYihui Zhai, Ling Chen, Meike Hömme, et al.
Plos One|August 15, 2015
Clinical Research in Vulnerable Populations: Variability and Focus of Institutional Review Boards' ResponsesBärbel Kästner, Simone Behre, Nadine Lutz, et al.
Orphanet Journal of Rare Diseases|December 24, 2015
A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type INikolas Boy, Jana Heringer, Gisela Haege, et al.
JIMD Reports|June 27, 2019
Formation of 3-hydroxyglutaric acid in glutaric aciduria type I: in vitro participation of medium chain acyl-CoA dehydrogenaseVerena Peters, Marina Morath, Matthias Mack, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuriaSven F Garbade, Nan Shen, Nastassja Himmelreich, et al.
Experimental Neurology|April 28, 2020
Chronic hyperammonemia causes a hypoglutamatergic and hyperGABAergic metabolic state associated with neurobehavioral abnormalities in zebrafish larvaeJoris Probst, Stefan Kölker, Jürgen G Okun, et al.
Journal of Inherited Metabolic Disease|May 4, 2012
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening resultJ Gerard Loeber, Peter Burgard, Martina C Cornel, et al.
The European Journal of Neuroscience|August 3, 2002
NMDA receptor activation and respiratory chain complex V inhibition contribute to neurodegeneration in d-2-hydroxyglutaric aciduriaStefan Kölker, Verena Pawlak, Barbara Ahlemeyer, et al.
Pageof 39

Showing results (121-130 of 381) with videos related to

Sort By:
Pageof 39
BMC Medical Education|November 28, 2024
A novel blended and interprofessional approach to pediatric emergency training: self-assessment, perception, and perceived long-term effectsRonny Lehmann, Michaela Klinke Petrowsky, Anke Seitz, et al.
JIMD Reports|May 6, 2015
Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn ScreeningGwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 7, 2010
Expression and function of matrix Gla protein in human peritoneal mesothelial cellsYihui Zhai, Ling Chen, Meike Hömme, et al.
Plos One|August 15, 2015
Clinical Research in Vulnerable Populations: Variability and Focus of Institutional Review Boards' ResponsesBärbel Kästner, Simone Behre, Nadine Lutz, et al.
Orphanet Journal of Rare Diseases|December 24, 2015
A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type INikolas Boy, Jana Heringer, Gisela Haege, et al.
JIMD Reports|June 27, 2019
Formation of 3-hydroxyglutaric acid in glutaric aciduria type I: in vitro participation of medium chain acyl-CoA dehydrogenaseVerena Peters, Marina Morath, Matthias Mack, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuriaSven F Garbade, Nan Shen, Nastassja Himmelreich, et al.
Experimental Neurology|April 28, 2020
Chronic hyperammonemia causes a hypoglutamatergic and hyperGABAergic metabolic state associated with neurobehavioral abnormalities in zebrafish larvaeJoris Probst, Stefan Kölker, Jürgen G Okun, et al.
Journal of Inherited Metabolic Disease|May 4, 2012
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening resultJ Gerard Loeber, Peter Burgard, Martina C Cornel, et al.
The European Journal of Neuroscience|August 3, 2002
NMDA receptor activation and respiratory chain complex V inhibition contribute to neurodegeneration in d-2-hydroxyglutaric aciduriaStefan Kölker, Verena Pawlak, Barbara Ahlemeyer, et al.
Pageof 39