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E Mayatepek

Showing results (1-10 of 178) with videos related to

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European Journal of Pediatrics|March 27, 1999
5-Oxoprolinuria in patients with and without defects in the gamma-glutamyl cycleE Mayatepek
European Journal of Pediatrics|November 18, 2000
Leukotriene C4 synthesis deficiency: a member of a probably underdiagnosed new group of neurometabolic diseasesE Mayatepek
Journal of Inherited Metabolic Disease|May 11, 1999
Metabolic decompensation and lactic acidosis in propionic acidaemia complicated by thiamine deficiencyE Mayatepek, A Schulze
Neuropediatrics|October 12, 2005
Neurological manifestations in lysosomal storage disorders - from pathology to first therapeutic possibilitiesB Hoffmann, E Mayatepek
Journal of Inherited Metabolic Disease|August 1, 1998
Lipoxygenase metabolites in amniotic fluid of patients with Zellweger syndromeE Mayatepek, C Jakobs
Biochemical and Biophysical Research Communications|October 3, 1996
Defective degradation of leukotrienes in peroxisomal-deficient human hepatocytesE Mayatepek, B Tiepelmann
Journal of Inherited Metabolic Disease|November 5, 1997
Sarcosinaemia in a patient with severe progressive neurological damage and hypertrophic cardiomyopathyT Meissner, E Mayatepek
European Journal of Pediatrics|August 13, 1999
Recurrent excessive transient hypertriglyceridaemiaT Meissner, E Mayatepek
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1993
Increased excretion of endogenous urinary leukotriene E4 in extrahepatic cholestasisE Mayatepek, G Pecher
European Journal of Pediatrics|August 1, 1998
Mannose supplementation in carbohydrate-deficient glycoprotein syndrome type I and phosphomannomutase deficiencyE Mayatepek, D Kohlmüller
Pageof 18

Showing results (1-10 of 178) with videos related to

Sort By:
Pageof 18
European Journal of Pediatrics|March 27, 1999
5-Oxoprolinuria in patients with and without defects in the gamma-glutamyl cycleE Mayatepek
European Journal of Pediatrics|November 18, 2000
Leukotriene C4 synthesis deficiency: a member of a probably underdiagnosed new group of neurometabolic diseasesE Mayatepek
Journal of Inherited Metabolic Disease|May 11, 1999
Metabolic decompensation and lactic acidosis in propionic acidaemia complicated by thiamine deficiencyE Mayatepek, A Schulze
Neuropediatrics|October 12, 2005
Neurological manifestations in lysosomal storage disorders - from pathology to first therapeutic possibilitiesB Hoffmann, E Mayatepek
Journal of Inherited Metabolic Disease|August 1, 1998
Lipoxygenase metabolites in amniotic fluid of patients with Zellweger syndromeE Mayatepek, C Jakobs
Biochemical and Biophysical Research Communications|October 3, 1996
Defective degradation of leukotrienes in peroxisomal-deficient human hepatocytesE Mayatepek, B Tiepelmann
Journal of Inherited Metabolic Disease|November 5, 1997
Sarcosinaemia in a patient with severe progressive neurological damage and hypertrophic cardiomyopathyT Meissner, E Mayatepek
European Journal of Pediatrics|August 13, 1999
Recurrent excessive transient hypertriglyceridaemiaT Meissner, E Mayatepek
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1993
Increased excretion of endogenous urinary leukotriene E4 in extrahepatic cholestasisE Mayatepek, G Pecher
European Journal of Pediatrics|August 1, 1998
Mannose supplementation in carbohydrate-deficient glycoprotein syndrome type I and phosphomannomutase deficiencyE Mayatepek, D Kohlmüller
Pageof 18