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F Hoffmann

Showing results (331-340 of 1,255) with videos related to

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Journal of Orthopaedic Surgery and Research|January 16, 2013
Recombinant human Bone Morphogenetic Protein-2 (rhBMP-2) in posterolateral lumbar spine fusion: complications in the elderlyMartin F Hoffmann, Clifford B Jones, Debra L Sietsema
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 28, 2022
Insights on the Lewis Superacid Al(OTeF<sub>5</sub> )<sub>3</sub> : Solvent Adducts, Characterization and PropertiesKurt F Hoffmann, Anja Wiesner, Simon Steinhauer, et al.
American Journal of Medical Genetics. Part A|March 28, 2013
Prenatal presentation and diagnostic evaluation of suspected Smith-Lemli-Opitz (RSH) syndromeDorothea Haas, Gisela Haege, Georg F Hoffmann, et al.
BMJ Open|July 18, 2018
Publication status of completed registered studies in paediatric appendicitis: a cross-sectional analysisThomas Breil, Michael Boettcher, Georg F Hoffmann, et al.
Immunology Today|August 23, 2000
Immunopathology of schistosomiasis mansoni in mice and menA W Cheever, K F Hoffmann, T A Wynn
Journal of Inherited Metabolic Disease|July 15, 2000
Methylmalonic acid induces excitotoxic neuronal damage in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Evaluation of trigger factors of acute encephalopathy in glutaric aciduria type I: fever and tumour necrosis factor-alphaS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Neurosurgery|October 3, 1999
Initial report on the limited value of hypoglossal nerve transfer to treat brachial plexus root avulsionsM J Malessy, C F Hoffmann, R T Thomeer
Pediatric Research|April 12, 2000
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, B Ahlemeyer, J Krieglstein, et al.
Clinical Chemistry|July 27, 2001
Spectrophotometric microassay for delta-aminolevulinate dehydratase in dried-blood spots as confirmation for hereditary tyrosinemia type IA Schulze, D Frommhold, G F Hoffmann, et al.
Pageof 126

Showing results (331-340 of 1,255) with videos related to

Sort By:
Pageof 126
Journal of Orthopaedic Surgery and Research|January 16, 2013
Recombinant human Bone Morphogenetic Protein-2 (rhBMP-2) in posterolateral lumbar spine fusion: complications in the elderlyMartin F Hoffmann, Clifford B Jones, Debra L Sietsema
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 28, 2022
Insights on the Lewis Superacid Al(OTeF<sub>5</sub> )<sub>3</sub> : Solvent Adducts, Characterization and PropertiesKurt F Hoffmann, Anja Wiesner, Simon Steinhauer, et al.
American Journal of Medical Genetics. Part A|March 28, 2013
Prenatal presentation and diagnostic evaluation of suspected Smith-Lemli-Opitz (RSH) syndromeDorothea Haas, Gisela Haege, Georg F Hoffmann, et al.
BMJ Open|July 18, 2018
Publication status of completed registered studies in paediatric appendicitis: a cross-sectional analysisThomas Breil, Michael Boettcher, Georg F Hoffmann, et al.
Immunology Today|August 23, 2000
Immunopathology of schistosomiasis mansoni in mice and menA W Cheever, K F Hoffmann, T A Wynn
Journal of Inherited Metabolic Disease|July 15, 2000
Methylmalonic acid induces excitotoxic neuronal damage in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Evaluation of trigger factors of acute encephalopathy in glutaric aciduria type I: fever and tumour necrosis factor-alphaS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Neurosurgery|October 3, 1999
Initial report on the limited value of hypoglossal nerve transfer to treat brachial plexus root avulsionsM J Malessy, C F Hoffmann, R T Thomeer
Pediatric Research|April 12, 2000
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, B Ahlemeyer, J Krieglstein, et al.
Clinical Chemistry|July 27, 2001
Spectrophotometric microassay for delta-aminolevulinate dehydratase in dried-blood spots as confirmation for hereditary tyrosinemia type IA Schulze, D Frommhold, G F Hoffmann, et al.
Pageof 126