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F Hoffmann

Showing results (821-830 of 1,255) with videos related to

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Frontiers in Oncology|June 9, 2020
Mitochondrial Dysfunction Inhibits Hypoxia-Induced HIF-1α Stabilization and Expression of Its Downstream TargetsMarike W van Gisbergen, Kelly Offermans, An M Voets, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Atypical case of Aicardi-Goutières syndrome with late-onset myoclonic statusAndrea Berger, Christiane Schroeter, Adelheid Wiemer-Kruel, et al.
Child Psychiatry and Human Development|May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidityG Engelmann, D Erhard, M Petersen, et al.
Neuropediatrics|August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?A C Muntau, W Röschinger, A Merkenschlager, et al.
Bone Marrow Transplantation|August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioningC F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]F K Trefz, G F Hoffmann, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type IRoland Posset, Silvana Opp, Eduard A Struys, et al.
Autophagy|November 24, 2021
Quantitative retrospective natural history modeling of <i>WDR45</i>-related developmental and epileptic encephalopathy - a systematic cross-sectional analysis of 160 published casesAfshin Saffari, Julian Schröter, Sven F Garbade, et al.
European Journal of Pediatrics|March 16, 2022
Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screeningUlrike Mütze, Uta Nennstiel, Birgit Odenwald, et al.
Der Nervenarzt|January 22, 2015
[Tryptophan immunoadsorption for multiple sclerosis and neuromyelitis optica: therapy option for acute relapses during pregnancy and breastfeeding]F Hoffmann, A Kraft, F Heigl, et al.
Pageof 126

Showing results (821-830 of 1,255) with videos related to

Sort By:
Pageof 126
Frontiers in Oncology|June 9, 2020
Mitochondrial Dysfunction Inhibits Hypoxia-Induced HIF-1α Stabilization and Expression of Its Downstream TargetsMarike W van Gisbergen, Kelly Offermans, An M Voets, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Atypical case of Aicardi-Goutières syndrome with late-onset myoclonic statusAndrea Berger, Christiane Schroeter, Adelheid Wiemer-Kruel, et al.
Child Psychiatry and Human Development|May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidityG Engelmann, D Erhard, M Petersen, et al.
Neuropediatrics|August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?A C Muntau, W Röschinger, A Merkenschlager, et al.
Bone Marrow Transplantation|August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioningC F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]F K Trefz, G F Hoffmann, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type IRoland Posset, Silvana Opp, Eduard A Struys, et al.
Autophagy|November 24, 2021
Quantitative retrospective natural history modeling of <i>WDR45</i>-related developmental and epileptic encephalopathy - a systematic cross-sectional analysis of 160 published casesAfshin Saffari, Julian Schröter, Sven F Garbade, et al.
European Journal of Pediatrics|March 16, 2022
Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screeningUlrike Mütze, Uta Nennstiel, Birgit Odenwald, et al.
Der Nervenarzt|January 22, 2015
[Tryptophan immunoadsorption for multiple sclerosis and neuromyelitis optica: therapy option for acute relapses during pregnancy and breastfeeding]F Hoffmann, A Kraft, F Heigl, et al.
Pageof 126