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E Mayatepek

Showing results (41-50 of 178) with videos related to

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Journal of Inherited Metabolic Disease|January 14, 1998
Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiencyE Mayatepek, H G Koch, G F Hoffmann
Journal of Inherited Metabolic Disease|February 11, 2005
Severe hyperhomocysteinaemia and 5-oxoprolinuria secondary to antiproliferative and antimicrobial drug treatmentB Schwahn, G Kameda, R Wessalowski, et al.
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
Molecular Genetics and Metabolism|December 26, 2001
Improving treatment of guanidinoacetate methyltransferase deficiency: reduction of guanidinoacetic acid in body fluids by arginine restriction and ornithine supplementationA Schulze, F Ebinger, D Rating, et al.
Klinische Padiatrie|December 16, 2016
Need for Better Diabetes Treatment: The Therapeutic Potential of NMDA Receptor AntagonistsA Welters, E Lammert, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Effect of plasma alpha-tocopherol on leukotriene E4 excretion in genetic vitamin E deficiencyA Kohlschütter, E Mayatepek, B Finckh, et al.
Pediatric Hematology and Oncology|July 17, 2001
Delta-storage pool disease in infancy with absence of blood serotonin associated with psychomotor retardationG Engelmann, E Morgenstern, N Wolf, et al.
European Journal of Pediatrics|November 11, 1998
Effects of ascorbic acid and low-protein diet in alkaptonuriaE Mayatepek, K Kallas, A Anninos, et al.
Klinische Padiatrie|February 19, 2010
Bloody nipple discharge (BND) in an 8 months old girl and a 9 months old male--rational diagnostic approachS Harmsen, E Mayatepek, D Klee, et al.
Pediatric Neurology|March 1, 1991
Long-term L-carnitine treatment in isovaleric acidemiaE Mayatepek, T W Kurczynski, C L Hoppel
Pageof 18

Showing results (41-50 of 178) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|January 14, 1998
Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiencyE Mayatepek, H G Koch, G F Hoffmann
Journal of Inherited Metabolic Disease|February 11, 2005
Severe hyperhomocysteinaemia and 5-oxoprolinuria secondary to antiproliferative and antimicrobial drug treatmentB Schwahn, G Kameda, R Wessalowski, et al.
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
Molecular Genetics and Metabolism|December 26, 2001
Improving treatment of guanidinoacetate methyltransferase deficiency: reduction of guanidinoacetic acid in body fluids by arginine restriction and ornithine supplementationA Schulze, F Ebinger, D Rating, et al.
Klinische Padiatrie|December 16, 2016
Need for Better Diabetes Treatment: The Therapeutic Potential of NMDA Receptor AntagonistsA Welters, E Lammert, E Mayatepek, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Effect of plasma alpha-tocopherol on leukotriene E4 excretion in genetic vitamin E deficiencyA Kohlschütter, E Mayatepek, B Finckh, et al.
Pediatric Hematology and Oncology|July 17, 2001
Delta-storage pool disease in infancy with absence of blood serotonin associated with psychomotor retardationG Engelmann, E Morgenstern, N Wolf, et al.
European Journal of Pediatrics|November 11, 1998
Effects of ascorbic acid and low-protein diet in alkaptonuriaE Mayatepek, K Kallas, A Anninos, et al.
Klinische Padiatrie|February 19, 2010
Bloody nipple discharge (BND) in an 8 months old girl and a 9 months old male--rational diagnostic approachS Harmsen, E Mayatepek, D Klee, et al.
Pediatric Neurology|March 1, 1991
Long-term L-carnitine treatment in isovaleric acidemiaE Mayatepek, T W Kurczynski, C L Hoppel
Pageof 18