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G F Hoffmann

Showing results (71-80 of 214) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
5-Oxoprolinase deficiency associated with severe psychomotor developmental delay, failure to thrive, microcephaly and microcytic anaemiaE Mayatepek, G F Hoffmann, A Larsson, et al.
Klinische Padiatrie|November 26, 1999
[Application of indirect calorimetry in monitoring feeding of low birth-weight preterm infants]T Krämer, T Böhler, A R Janecke, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Emergency management of inherited metabolic diseasesV Prietsch, M Lindner, J Zschocke, et al.
Early Human Development|May 13, 1999
Increased energy expenditure and fecal fat excretion do not impair weight gain in small-for-gestational-age preterm infantsT Böhler, T Krämer, A R Janecke, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.
The Journal of Pediatrics|March 1, 1996
Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?J Meyburg, E Mayatepek, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Neonatal screening for glutaric aciduria type I: strategies to proceedM Lindner, S Ho, J Fang-Hoffmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 19, 2008
A novel mutation (c.64_65delGGinsAACC [p.G21fsX66]) in the GTP cyclohydrolase 1 gene that causes Segawa diseaseM von Mering, H Gabriel, T Opladen, et al.
Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.
The European Journal of Neuroscience|June 26, 2001
Potentiation of 3-hydroxyglutarate neurotoxicity following induction of astrocytic iNOS in neonatal rat hippocampal culturesS Kölker, B Ahlemeyer, R Hühne, et al.
Pageof 22

Showing results (71-80 of 214) with videos related to

Sort By:
Pageof 22
Journal of Inherited Metabolic Disease|January 1, 1995
5-Oxoprolinase deficiency associated with severe psychomotor developmental delay, failure to thrive, microcephaly and microcytic anaemiaE Mayatepek, G F Hoffmann, A Larsson, et al.
Klinische Padiatrie|November 26, 1999
[Application of indirect calorimetry in monitoring feeding of low birth-weight preterm infants]T Krämer, T Böhler, A R Janecke, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Emergency management of inherited metabolic diseasesV Prietsch, M Lindner, J Zschocke, et al.
Early Human Development|May 13, 1999
Increased energy expenditure and fecal fat excretion do not impair weight gain in small-for-gestational-age preterm infantsT Böhler, T Krämer, A R Janecke, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.
The Journal of Pediatrics|March 1, 1996
Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?J Meyburg, E Mayatepek, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Neonatal screening for glutaric aciduria type I: strategies to proceedM Lindner, S Ho, J Fang-Hoffmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 19, 2008
A novel mutation (c.64_65delGGinsAACC [p.G21fsX66]) in the GTP cyclohydrolase 1 gene that causes Segawa diseaseM von Mering, H Gabriel, T Opladen, et al.
Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.
The European Journal of Neuroscience|June 26, 2001
Potentiation of 3-hydroxyglutarate neurotoxicity following induction of astrocytic iNOS in neonatal rat hippocampal culturesS Kölker, B Ahlemeyer, R Hühne, et al.
Pageof 22