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G F Hoffmann

Showing results (51-60 of 214) with videos related to

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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.
Neuropediatrics|June 25, 1998
Cerebrospinal fluid investigations for neurometabolic disordersG F Hoffmann, R A Surtees, R A Wevers
Journal of Medical Genetics|March 4, 2000
Mutation analysis in glutaric aciduria type IJ Zschocke, E Quak, P Guldberg, et al.
Diabetologia|August 10, 1999
Impaired deformability of erythrocytes and neutrophils in children with newly diagnosed insulin-dependent diabetes mellitusO Linderkamp, P Ruef, E P Zilow, et al.
The Journal of Pediatrics|February 15, 2001
Acute encephalopathy despite early therapy in a patient with homozygosity for E365K in the glutaryl-coenzyme A dehydrogenase geneS Kölker, V T Ramaekers, J Zschocke, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Neurotransmitter metabolites in CSF: an external quality control schemeC Bräutigam, C Weykamp, G F Hoffmann, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1992
[Kawasaki syndrome. Association with exposure to carpet shampoo and successful therapy with immunoglobulins in the second week of the illness]E Blum-Hoffmann, G F Hoffmann, A Wessel, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Mevalonate kinase deficiency in a dizygotic twin with mild mevalonic aciduriaK M Gibson, G F Hoffmann, L Sweetman, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Plasma concentrations of phenyllactic acid in phenylketonuriaP C Clemens, M H Schünemann, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Segregation of the N301T mutation in the family of the index patient with mevalonate kinase deficiencyB Goebel-Schreiner, R Schreiner, G F Hoffmann, et al.
Pageof 22

Showing results (51-60 of 214) with videos related to

Sort By:
Pageof 22
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.
Neuropediatrics|June 25, 1998
Cerebrospinal fluid investigations for neurometabolic disordersG F Hoffmann, R A Surtees, R A Wevers
Journal of Medical Genetics|March 4, 2000
Mutation analysis in glutaric aciduria type IJ Zschocke, E Quak, P Guldberg, et al.
Diabetologia|August 10, 1999
Impaired deformability of erythrocytes and neutrophils in children with newly diagnosed insulin-dependent diabetes mellitusO Linderkamp, P Ruef, E P Zilow, et al.
The Journal of Pediatrics|February 15, 2001
Acute encephalopathy despite early therapy in a patient with homozygosity for E365K in the glutaryl-coenzyme A dehydrogenase geneS Kölker, V T Ramaekers, J Zschocke, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Neurotransmitter metabolites in CSF: an external quality control schemeC Bräutigam, C Weykamp, G F Hoffmann, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1992
[Kawasaki syndrome. Association with exposure to carpet shampoo and successful therapy with immunoglobulins in the second week of the illness]E Blum-Hoffmann, G F Hoffmann, A Wessel, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Mevalonate kinase deficiency in a dizygotic twin with mild mevalonic aciduriaK M Gibson, G F Hoffmann, L Sweetman, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Plasma concentrations of phenyllactic acid in phenylketonuriaP C Clemens, M H Schünemann, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Segregation of the N301T mutation in the family of the index patient with mevalonate kinase deficiencyB Goebel-Schreiner, R Schreiner, G F Hoffmann, et al.
Pageof 22