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Janbernd Kirschner

Showing results (31-40 of 173) with videos related to

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FEBS Letters|December 14, 2017
Mitochondrial fatty acid biosynthesis and muscle fiber plasticity in very long-chain acyl-CoA dehydrogenase-deficient miceSara Tucci, Nadja Mingirulli, Zeinab Wehbe, et al.
Hepatology (Baltimore, Md.)|December 26, 2006
Uridine supplementation antagonizes zalcitabine-induced microvesicular steatohepatitis in miceDirk Lebrecht, Yetlanezi A Vargas-Infante, Bernhard Setzer, et al.
Journal of Musculoskeletal & Neuronal Interactions|March 1, 2023
Mechanographic analysis of the timed 4 stair climb test - methodology and reference data of healthy children and adolescentsDavid C Schorling, Rainer Rawer, Imke Kuhlmann, et al.
Neurology|June 26, 2019
Discrepancy in redetermination of <i>SMN2</i> copy numbers in children with SMADavid Christof Schorling, Jutta Becker, Astrid Pechmann, et al.
European Journal of Epidemiology|February 29, 2020
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysisErik Landfeldt, Rachel Thompson, Thomas Sejersen, et al.
Arthritis and Rheumatism|January 1, 2008
Uridine supplementation antagonizes zidovudine-induced mitochondrial myopathy and hyperlactatemia in miceDirk Lebrecht, Catherine Deveaud, Bertrand Beauvoit, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 26, 2013
Whole-body vibration training in children with Duchenne muscular dystrophy and spinal muscular atrophyJulia Vry, Isabel J Schubert, Oliver Semler, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 6, 2021
Post-dural puncture headache-a single-centre analysis in paediatric patients with and without SMADavid C Schorling, Astrid Pechmann, Matthias Eckenweiler, et al.
Cytoskeleton (Hoboken, N.J.)|July 19, 2018
Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family studyKatharina Neubauer, Doris Boeckelmann, Udo Koehler, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|July 8, 2009
Mitochondrial tubulopathy in tenofovir disoproxil fumarate-treated ratsDirk Lebrecht, Ana C Venhoff, Janbernd Kirschner, et al.
Pageof 18

Showing results (31-40 of 173) with videos related to

Sort By:
Pageof 18
FEBS Letters|December 14, 2017
Mitochondrial fatty acid biosynthesis and muscle fiber plasticity in very long-chain acyl-CoA dehydrogenase-deficient miceSara Tucci, Nadja Mingirulli, Zeinab Wehbe, et al.
Hepatology (Baltimore, Md.)|December 26, 2006
Uridine supplementation antagonizes zalcitabine-induced microvesicular steatohepatitis in miceDirk Lebrecht, Yetlanezi A Vargas-Infante, Bernhard Setzer, et al.
Journal of Musculoskeletal & Neuronal Interactions|March 1, 2023
Mechanographic analysis of the timed 4 stair climb test - methodology and reference data of healthy children and adolescentsDavid C Schorling, Rainer Rawer, Imke Kuhlmann, et al.
Neurology|June 26, 2019
Discrepancy in redetermination of <i>SMN2</i> copy numbers in children with SMADavid Christof Schorling, Jutta Becker, Astrid Pechmann, et al.
European Journal of Epidemiology|February 29, 2020
Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysisErik Landfeldt, Rachel Thompson, Thomas Sejersen, et al.
Arthritis and Rheumatism|January 1, 2008
Uridine supplementation antagonizes zidovudine-induced mitochondrial myopathy and hyperlactatemia in miceDirk Lebrecht, Catherine Deveaud, Bertrand Beauvoit, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 26, 2013
Whole-body vibration training in children with Duchenne muscular dystrophy and spinal muscular atrophyJulia Vry, Isabel J Schubert, Oliver Semler, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 6, 2021
Post-dural puncture headache-a single-centre analysis in paediatric patients with and without SMADavid C Schorling, Astrid Pechmann, Matthias Eckenweiler, et al.
Cytoskeleton (Hoboken, N.J.)|July 19, 2018
Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family studyKatharina Neubauer, Doris Boeckelmann, Udo Koehler, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|July 8, 2009
Mitochondrial tubulopathy in tenofovir disoproxil fumarate-treated ratsDirk Lebrecht, Ana C Venhoff, Janbernd Kirschner, et al.
Pageof 18