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E Mayatepek

Showing results (11-20 of 178) with videos related to

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Journal of Inherited Metabolic Disease|July 15, 2000
Biochemical and molecular studies in mild flavin monooxygenase 3 deficiencyJ Zschocke, E Mayatepek
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 26, 1999
Increased urinary excretion of LTB4 and omega-carboxy-LTB4 in patients with Zellweger syndromeE Mayatepek, B Flock
Klinische Padiatrie|January 25, 2006
[Fabry disease--a provocation for pediatrics]B Hoffmann, E Mayatepek
Acta Paediatrica (Oslo, Norway : 1992)|December 10, 1998
Transient trimethylaminuria in childhoodE Mayatepek, D Kohlmüller
Lancet (London, England)|November 20, 1998
Leukotriene C4-synthesis deficiency: a new inborn error of metabolism linked to a fatal developmental syndromeE Mayatepek, B Flock
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1996
Defective hepatobiliary leukotriene elimination in patients with the Dubin-Johnson syndromeE Mayatepek, W D Lehmann
Journal of Inherited Metabolic Disease|August 1, 1998
Defective oxidation of hydroxyeicosatetraenoic acids in the liver of patients with Zellweger syndromeE Mayatepek, R J Wanders
Archives of Disease in Childhood|June 1, 1995
Increased generation of cysteinyl leukotrienes in Kawasaki diseaseE Mayatepek, W D Lehmann
Pediatric Research|January 1, 1996
12- and 15-hydroxyeicosatetraenoic acid are excreted in the urine of peroxisome-deficient patients: evidence for peroxisomal metabolism in vivoE Mayatepek, W D Lehmann
Pediatric Research|January 1, 1995
Leukotrienes: biosynthesis, metabolism, and pathophysiologic significanceE Mayatepek, G F Hoffmann
Pageof 18

Showing results (11-20 of 178) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|July 15, 2000
Biochemical and molecular studies in mild flavin monooxygenase 3 deficiencyJ Zschocke, E Mayatepek
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 26, 1999
Increased urinary excretion of LTB4 and omega-carboxy-LTB4 in patients with Zellweger syndromeE Mayatepek, B Flock
Klinische Padiatrie|January 25, 2006
[Fabry disease--a provocation for pediatrics]B Hoffmann, E Mayatepek
Acta Paediatrica (Oslo, Norway : 1992)|December 10, 1998
Transient trimethylaminuria in childhoodE Mayatepek, D Kohlmüller
Lancet (London, England)|November 20, 1998
Leukotriene C4-synthesis deficiency: a new inborn error of metabolism linked to a fatal developmental syndromeE Mayatepek, B Flock
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1996
Defective hepatobiliary leukotriene elimination in patients with the Dubin-Johnson syndromeE Mayatepek, W D Lehmann
Journal of Inherited Metabolic Disease|August 1, 1998
Defective oxidation of hydroxyeicosatetraenoic acids in the liver of patients with Zellweger syndromeE Mayatepek, R J Wanders
Archives of Disease in Childhood|June 1, 1995
Increased generation of cysteinyl leukotrienes in Kawasaki diseaseE Mayatepek, W D Lehmann
Pediatric Research|January 1, 1996
12- and 15-hydroxyeicosatetraenoic acid are excreted in the urine of peroxisome-deficient patients: evidence for peroxisomal metabolism in vivoE Mayatepek, W D Lehmann
Pediatric Research|January 1, 1995
Leukotrienes: biosynthesis, metabolism, and pathophysiologic significanceE Mayatepek, G F Hoffmann
Pageof 18