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E Mayatepek

Showing results (61-70 of 178) with videos related to

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Pediatric Research|January 3, 2001
Postnatal changes in neonatal acylcarnitine profileJ Meyburg, A Schulze, D Kohlmueller, et al.
Molecular Genetics and Metabolism|May 15, 2001
Tetrahydrobiopterin responsiveness in phenylketonuria differs between patients with the same genotypeM Lindner, D Haas, E Mayatepek, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|December 28, 2012
Successful management of neonatal hemochromatosis by exchange transfusion and immunoglobulin: a case reportF Babor, B Hadzik, H Stannigel, et al.
Klinische Padiatrie|February 6, 2013
Pancreatitis in maple syrup urine disease -- a rare and easily overseen complicationF Baertling, E Mayatepek, A Schlune, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 18, 1999
Dialysis in neonates with inborn errors of metabolismF Schaefer, E Straube, J Oh, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Fatal genetic defect causing Wolman diseaseE Mayatepek, U Seedorf, H Wiebusch, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
3-Methylglutaconic aciduria associated with hepatosplenomegaly, macrocytic anaemia, fever episodes, recurrent infections, cervical lymphadenopathy and progressive decrease of physical performanceM H Holtmann, P R Galle, W Stremmel, et al.
Lancet (London, England)|October 16, 1993
Leukotrienes in the pathophysiology of kwashiorkorE Mayatepek, K Becker, L Gana, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 14, 1997
Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type IE Mayatepek, M Schröder, D Kohlmüller, et al.
Journal of Inherited Metabolic Disease|December 25, 2004
S-Acetylglutathione normalizes intracellular glutathione content in cultured fibroblasts from patients with glutathione synthetase deficiencyJ G Okun, S Sauer, S Bähr, et al.
Pageof 18

Showing results (61-70 of 178) with videos related to

Sort By:
Pageof 18
Pediatric Research|January 3, 2001
Postnatal changes in neonatal acylcarnitine profileJ Meyburg, A Schulze, D Kohlmueller, et al.
Molecular Genetics and Metabolism|May 15, 2001
Tetrahydrobiopterin responsiveness in phenylketonuria differs between patients with the same genotypeM Lindner, D Haas, E Mayatepek, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|December 28, 2012
Successful management of neonatal hemochromatosis by exchange transfusion and immunoglobulin: a case reportF Babor, B Hadzik, H Stannigel, et al.
Klinische Padiatrie|February 6, 2013
Pancreatitis in maple syrup urine disease -- a rare and easily overseen complicationF Baertling, E Mayatepek, A Schlune, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 18, 1999
Dialysis in neonates with inborn errors of metabolismF Schaefer, E Straube, J Oh, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Fatal genetic defect causing Wolman diseaseE Mayatepek, U Seedorf, H Wiebusch, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
3-Methylglutaconic aciduria associated with hepatosplenomegaly, macrocytic anaemia, fever episodes, recurrent infections, cervical lymphadenopathy and progressive decrease of physical performanceM H Holtmann, P R Galle, W Stremmel, et al.
Lancet (London, England)|October 16, 1993
Leukotrienes in the pathophysiology of kwashiorkorE Mayatepek, K Becker, L Gana, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 14, 1997
Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type IE Mayatepek, M Schröder, D Kohlmüller, et al.
Journal of Inherited Metabolic Disease|December 25, 2004
S-Acetylglutathione normalizes intracellular glutathione content in cultured fibroblasts from patients with glutathione synthetase deficiencyJ G Okun, S Sauer, S Bähr, et al.
Pageof 18