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F HOFFMANN

Showing results (381-390 of 1,073) with videos related to

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Journal of Inherited Metabolic Disease|September 3, 1999
Large heterozygous deletion masquerading as homozygous missense mutation: a pitfall in diagnostic mutation analysisJ Zschocke, E Quak, A Knauer, et al.
Klinische Padiatrie|March 1, 1993
[Glutaric acidemia/glutaric aciduria I as differential chorea minor diagnosis]R Voll, G F Hoffmann, C G Lipinski, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: anticholinergic drugs and botulinum toxin as additional therapeutic optionsA P Burlina, G Zara, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|June 26, 2013
Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemiaTamaris Zwickler, Alina Riderer, Gisela Haege, et al.
Zeitschrift Fur Rheumatologie|July 26, 2019
Reality of care for musculoskeletal diseases at the population level : Results of the PROCLAIR collaborative projectJ Callhoff, K Albrecht, F Hoffmann, et al.
Nature and Science of Sleep|April 27, 2013
The influence of emerging low mood symptoms on sleep in children: a pilot studyDeirdre A Conroy, Anameti Usoro, Robert F Hoffmann, et al.
The Pediatric Infectious Disease Journal|January 22, 2000
Comparison of ritonavir plus saquinavir- and nelfinavir plus saquinavir-containing regimens as salvage therapy in children with human immunodeficiency type 1 infectionF Hoffmann, G Notheis, U Wintergerst, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Sensitivity and specificity of free and total glutaric acid and 3-hydroxyglutaric acid measurements by stable-isotope dilution assays for the diagnosis of glutaric aciduria type II Baric, L Wagner, P Feyh, et al.
Neuropediatrics|April 29, 1998
4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolismK M Gibson, G F Hoffmann, A K Hodson, et al.
Pediatrics|June 5, 2003
Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implicationsAndreas Schulze, Martin Lindner, Dirk Kohlmüller, et al.
Pageof 108

Showing results (381-390 of 1,073) with videos related to

Sort By:
Pageof 108
Journal of Inherited Metabolic Disease|September 3, 1999
Large heterozygous deletion masquerading as homozygous missense mutation: a pitfall in diagnostic mutation analysisJ Zschocke, E Quak, A Knauer, et al.
Klinische Padiatrie|March 1, 1993
[Glutaric acidemia/glutaric aciduria I as differential chorea minor diagnosis]R Voll, G F Hoffmann, C G Lipinski, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: anticholinergic drugs and botulinum toxin as additional therapeutic optionsA P Burlina, G Zara, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|June 26, 2013
Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemiaTamaris Zwickler, Alina Riderer, Gisela Haege, et al.
Zeitschrift Fur Rheumatologie|July 26, 2019
Reality of care for musculoskeletal diseases at the population level : Results of the PROCLAIR collaborative projectJ Callhoff, K Albrecht, F Hoffmann, et al.
Nature and Science of Sleep|April 27, 2013
The influence of emerging low mood symptoms on sleep in children: a pilot studyDeirdre A Conroy, Anameti Usoro, Robert F Hoffmann, et al.
The Pediatric Infectious Disease Journal|January 22, 2000
Comparison of ritonavir plus saquinavir- and nelfinavir plus saquinavir-containing regimens as salvage therapy in children with human immunodeficiency type 1 infectionF Hoffmann, G Notheis, U Wintergerst, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Sensitivity and specificity of free and total glutaric acid and 3-hydroxyglutaric acid measurements by stable-isotope dilution assays for the diagnosis of glutaric aciduria type II Baric, L Wagner, P Feyh, et al.
Neuropediatrics|April 29, 1998
4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolismK M Gibson, G F Hoffmann, A K Hodson, et al.
Pediatrics|June 5, 2003
Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implicationsAndreas Schulze, Martin Lindner, Dirk Kohlmüller, et al.
Pageof 108