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G F Hoffmann

Showing results (31-40 of 214) with videos related to

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Der Nervenarzt|March 31, 1999
[Enzyme defects of the urea cycle in differential acute encephalopathy diagnosis in adulthood. Diagnosis and current therapy concepts]S Schwarz, S Schwab, G F Hoffmann
Neuropediatrics|August 25, 2001
Inherited disorders of cholesterol biosynthesisD Haas, R I Kelley, G F Hoffmann
Journal of Inherited Metabolic Disease|January 14, 1998
Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiencyE Mayatepek, H G Koch, G F Hoffmann
European Journal of Pediatrics|September 1, 1995
Increased urinary excretion of dicarboxylic acids and 4-hydroxyphenyllactic acid in patients with Zellweger syndromeE Mayatepek, C K Seppel, G F Hoffmann
Minerva Pediatrica|January 31, 2009
High prevalence of vitamin D deficiency in young children in a highly sunny humid country: a global health problemA Bener, M Al-Ali, G F Hoffmann
Journal of Inherited Metabolic Disease|December 16, 2000
Erythropoietic and hepatic porphyriasU Gross, G F Hoffmann, M O Doss
The Journal of Pediatrics|March 10, 2001
L-dopa and selegiline for tyrosine hydroxylase deficiencyM Häussler, G F Hoffmann, R A Wevers
Journal of Inherited Metabolic Disease|July 24, 2007
Expanded newborn screening in Europe 2007O A Bodamer, G F Hoffmann, M Lindner
The Journal of Pediatrics|July 1, 1993
Enhanced urinary excretion of leukotriene E4 in patients with mevalonate kinase deficiencyE Mayatepek, G F Hoffmann, H J Bremer
Archives of Disease in Childhood|June 29, 2002
Nature and nurture in vitamin B12 deficiencyJ Zschocke, S Schindler, G F Hoffmann, et al.
Pageof 22

Showing results (31-40 of 214) with videos related to

Sort By:
Pageof 22
Der Nervenarzt|March 31, 1999
[Enzyme defects of the urea cycle in differential acute encephalopathy diagnosis in adulthood. Diagnosis and current therapy concepts]S Schwarz, S Schwab, G F Hoffmann
Neuropediatrics|August 25, 2001
Inherited disorders of cholesterol biosynthesisD Haas, R I Kelley, G F Hoffmann
Journal of Inherited Metabolic Disease|January 14, 1998
Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiencyE Mayatepek, H G Koch, G F Hoffmann
European Journal of Pediatrics|September 1, 1995
Increased urinary excretion of dicarboxylic acids and 4-hydroxyphenyllactic acid in patients with Zellweger syndromeE Mayatepek, C K Seppel, G F Hoffmann
Minerva Pediatrica|January 31, 2009
High prevalence of vitamin D deficiency in young children in a highly sunny humid country: a global health problemA Bener, M Al-Ali, G F Hoffmann
Journal of Inherited Metabolic Disease|December 16, 2000
Erythropoietic and hepatic porphyriasU Gross, G F Hoffmann, M O Doss
The Journal of Pediatrics|March 10, 2001
L-dopa and selegiline for tyrosine hydroxylase deficiencyM Häussler, G F Hoffmann, R A Wevers
Journal of Inherited Metabolic Disease|July 24, 2007
Expanded newborn screening in Europe 2007O A Bodamer, G F Hoffmann, M Lindner
The Journal of Pediatrics|July 1, 1993
Enhanced urinary excretion of leukotriene E4 in patients with mevalonate kinase deficiencyE Mayatepek, G F Hoffmann, H J Bremer
Archives of Disease in Childhood|June 29, 2002
Nature and nurture in vitamin B12 deficiencyJ Zschocke, S Schindler, G F Hoffmann, et al.
Pageof 22