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E Mayatepek

Showing results (81-90 of 140) with videos related to

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Journal of Inherited Metabolic Disease|May 27, 2008
Severe neurological crisis in a patient with hereditary tyrosinaemia type I after interruption of NTBC treatmentJ-U Schlump, C Perot, K Ketteler, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|January 1, 1990
Vitamin E status of Congolese children in a rural areaM D Laryea, E Mayatepek, P Brünninger, et al.
The Journal of Clinical Investigation|April 20, 1999
Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuriaJ Pietz, R Kreis, A Rupp, et al.
Neuropediatrics|September 13, 2006
Acute neuronopathic Gaucher disease complicated by fatal gastrointestinal bleedingB Hoffmann, B Schwahn, C B Knobbe, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 29, 2005
Aplasia cutis congenita of the scalp: how much therapy is necessary in large defects?B Bernbeck, J Schwabe, A Groninger, et al.
European Journal of Clinical Investigation|February 1, 1994
The diagnosis of pulmonary tuberculosis by gaschromatographic detection of tuberculostearic acid using flame ionisation detectorsA Herz, M Leichsenring, M Felten, et al.
The Journal of Pediatrics|February 5, 1999
Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiencyM Schuelke, E Mayatepek, M Inter, et al.
Archives of Disease in Childhood|February 24, 2001
Exercise induced hypoglycaemic hyperinsulinismT Meissner, T Otonkoski, R Feneberg, et al.
Chest|May 16, 2000
Urinary leukotriene E(4) levels are not increased prior to high-altitude pulmonary edemaP Bärtsch, U Eichenberger, P E Ballmer, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2U Spiekerkoetter, G Huener, T Baykal, et al.
Pageof 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
Journal of Inherited Metabolic Disease|May 27, 2008
Severe neurological crisis in a patient with hereditary tyrosinaemia type I after interruption of NTBC treatmentJ-U Schlump, C Perot, K Ketteler, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|January 1, 1990
Vitamin E status of Congolese children in a rural areaM D Laryea, E Mayatepek, P Brünninger, et al.
The Journal of Clinical Investigation|April 20, 1999
Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuriaJ Pietz, R Kreis, A Rupp, et al.
Neuropediatrics|September 13, 2006
Acute neuronopathic Gaucher disease complicated by fatal gastrointestinal bleedingB Hoffmann, B Schwahn, C B Knobbe, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 29, 2005
Aplasia cutis congenita of the scalp: how much therapy is necessary in large defects?B Bernbeck, J Schwabe, A Groninger, et al.
European Journal of Clinical Investigation|February 1, 1994
The diagnosis of pulmonary tuberculosis by gaschromatographic detection of tuberculostearic acid using flame ionisation detectorsA Herz, M Leichsenring, M Felten, et al.
The Journal of Pediatrics|February 5, 1999
Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiencyM Schuelke, E Mayatepek, M Inter, et al.
Archives of Disease in Childhood|February 24, 2001
Exercise induced hypoglycaemic hyperinsulinismT Meissner, T Otonkoski, R Feneberg, et al.
Chest|May 16, 2000
Urinary leukotriene E(4) levels are not increased prior to high-altitude pulmonary edemaP Bärtsch, U Eichenberger, P E Ballmer, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2U Spiekerkoetter, G Huener, T Baykal, et al.
Pageof 14