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Journal of Inherited Metabolic Disease
|
January 14, 1998
Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency
E 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 treatment
B 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 syndrome
E 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 supplementation
A Schulze, F Ebinger, D Rating, et al.
Klinische Padiatrie
|
December 16, 2016
Need for Better Diabetes Treatment: The Therapeutic Potential of NMDA Receptor Antagonists
A 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 deficiency
A 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 retardation
G Engelmann, E Morgenstern, N Wolf, et al.
European Journal of Pediatrics
|
November 11, 1998
Effects of ascorbic acid and low-protein diet in alkaptonuria
E 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 approach
S Harmsen, E Mayatepek, D Klee, et al.
Pediatric Neurology
|
March 1, 1991
Long-term L-carnitine treatment in isovaleric acidemia
E Mayatepek, T W Kurczynski, C L Hoppel
Page
of 18
Search research articles
Search
Showing results (41-50 of 178) with videos related to
Sort By:
Page
of 18
Journal of Inherited Metabolic Disease
|
January 14, 1998
Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency
E 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 treatment
B 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 syndrome
E 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 supplementation
A Schulze, F Ebinger, D Rating, et al.
Klinische Padiatrie
|
December 16, 2016
Need for Better Diabetes Treatment: The Therapeutic Potential of NMDA Receptor Antagonists
A 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 deficiency
A 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 retardation
G Engelmann, E Morgenstern, N Wolf, et al.
European Journal of Pediatrics
|
November 11, 1998
Effects of ascorbic acid and low-protein diet in alkaptonuria
E 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 approach
S Harmsen, E Mayatepek, D Klee, et al.
Pediatric Neurology
|
March 1, 1991
Long-term L-carnitine treatment in isovaleric acidemia
E Mayatepek, T W Kurczynski, C L Hoppel
Page
of 18