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G Okun

Showing results (51-60 of 165) with videos related to

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Neurochemistry International|February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)S W Sauer, S Kölker, G F Hoffmann, et al.
Pediatric Research|March 22, 2006
Phenylalanine reduces synaptic density in mixed cortical cultures from miceFriederike Hörster, Marina A Schwab, Sven W Sauer, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
International Journal of Neonatal Screening|March 27, 2024
New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening CenterGwendolyn Gramer, Saskia B Wortmann, Junmin Fang-Hoffmann, et al.
Clinical and Experimental Nephrology|November 4, 2015
Increased storage and secretion of phosphatidylcholines by senescent human peritoneal mesothelial cellsMaria Bartosova, Andras Rudolf, Sebastian Pichl, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maintenance treatment of glutaryl-CoA dehydrogenase deficiencyC Mühlhausen, G F Hoffmann, K A Strauss, et al.
European Journal of Neurology|April 14, 2020
Trimethylamine-N-oxide is elevated in the acute phase after ischaemic stroke and decreases within the first daysC Schneider, J G Okun, K V Schwarz, et al.
Gene|January 21, 2014
Diagnosis and therapeutic monitoring of inborn errors of creatine metabolism and transport using liquid chromatography-tandem mass spectrometry in urine, plasma and CSFDorothea Haas, Hongying Gan-Schreier, Claus-Dieter Langhans, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Science (New York, N.Y.)|September 15, 2018
Semisynthetic sensor proteins enable metabolic assays at the point of careQiuliyang Yu, Lin Xue, Julien Hiblot, et al.
Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:
Pageof 17
Neurochemistry International|February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)S W Sauer, S Kölker, G F Hoffmann, et al.
Pediatric Research|March 22, 2006
Phenylalanine reduces synaptic density in mixed cortical cultures from miceFriederike Hörster, Marina A Schwab, Sven W Sauer, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
International Journal of Neonatal Screening|March 27, 2024
New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening CenterGwendolyn Gramer, Saskia B Wortmann, Junmin Fang-Hoffmann, et al.
Clinical and Experimental Nephrology|November 4, 2015
Increased storage and secretion of phosphatidylcholines by senescent human peritoneal mesothelial cellsMaria Bartosova, Andras Rudolf, Sebastian Pichl, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maintenance treatment of glutaryl-CoA dehydrogenase deficiencyC Mühlhausen, G F Hoffmann, K A Strauss, et al.
European Journal of Neurology|April 14, 2020
Trimethylamine-N-oxide is elevated in the acute phase after ischaemic stroke and decreases within the first daysC Schneider, J G Okun, K V Schwarz, et al.
Gene|January 21, 2014
Diagnosis and therapeutic monitoring of inborn errors of creatine metabolism and transport using liquid chromatography-tandem mass spectrometry in urine, plasma and CSFDorothea Haas, Hongying Gan-Schreier, Claus-Dieter Langhans, et al.
Journal of Inherited Metabolic Disease|June 9, 2009
Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduriaD Haas, P Niklowitz, F Hörster, et al.
Science (New York, N.Y.)|September 15, 2018
Semisynthetic sensor proteins enable metabolic assays at the point of careQiuliyang Yu, Lin Xue, Julien Hiblot, et al.
Pageof 17