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Ertan Mayatepek

Showing results (1-10 of 289) with videos related to

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Deutsches Arzteblatt International|July 23, 2009
Fabry disease-often seen, rarely diagnosedBjörn Hoffmann, Ertan Mayatepek
European Journal of Pediatrics|January 26, 2002
Clinical and genetic heterogeneity in congenital hyperinsulinismThomas Meissner, Ertan Mayatepek
Journal of Inherited Metabolic Disease|September 16, 2010
Update on mitochondrial fatty acid oxidation disordersUte Spiekerkoetter, Ertan Mayatepek
Journal of Inherited Metabolic Disease|February 15, 2013
Hypertrichosis in presymptomatic mitochondrial diseaseFabian Baertling, Ertan Mayatepek, Felix Distelmaier
Clinical Chemistry and Laboratory Medicine|October 23, 2004
Odd-numbered long-chain fatty acids in erythrocyte phospholipids as long-term follow-up parameter in propionic acidemiaThomas Meissner, Michael Leichsenring, Ertan Mayatepek
Archives of Disease in Childhood|March 22, 2008
Probable idiopathic intracranial hypertension in pre-pubertal childrenFelix Distelmaier, Ertan Mayatepek, Daniel Tibussek
Best Practice & Research. Clinical Gastroenterology|October 20, 2010
Inborn errors of carbohydrate metabolismErtan Mayatepek, Björn Hoffmann, Thomas Meissner
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 18, 2009
Neonatal pleural empyema in an extremely low birth weight infantKlaus Lohmeier, Ertan Mayatepek, Thomas Hoehn
Pharmacogenetics|November 27, 2004
Benzydamine metabolism in vivo is impaired in patients with deficiency of flavin-containing monooxygenase 3Ertan Mayatepek, Bianca Flock, Johannes Zschocke
European Journal of Pediatrics|October 9, 2009
Significant increase of succinylacetone within the first 12 h of life in hereditary tyrosinemia type 1Jan-Ulrich Schlump, Ertan Mayatepek, Ute Spiekerkoetter
Pageof 29

Showing results (1-10 of 289) with videos related to

Sort By:
Pageof 29
Deutsches Arzteblatt International|July 23, 2009
Fabry disease-often seen, rarely diagnosedBjörn Hoffmann, Ertan Mayatepek
European Journal of Pediatrics|January 26, 2002
Clinical and genetic heterogeneity in congenital hyperinsulinismThomas Meissner, Ertan Mayatepek
Journal of Inherited Metabolic Disease|September 16, 2010
Update on mitochondrial fatty acid oxidation disordersUte Spiekerkoetter, Ertan Mayatepek
Journal of Inherited Metabolic Disease|February 15, 2013
Hypertrichosis in presymptomatic mitochondrial diseaseFabian Baertling, Ertan Mayatepek, Felix Distelmaier
Clinical Chemistry and Laboratory Medicine|October 23, 2004
Odd-numbered long-chain fatty acids in erythrocyte phospholipids as long-term follow-up parameter in propionic acidemiaThomas Meissner, Michael Leichsenring, Ertan Mayatepek
Archives of Disease in Childhood|March 22, 2008
Probable idiopathic intracranial hypertension in pre-pubertal childrenFelix Distelmaier, Ertan Mayatepek, Daniel Tibussek
Best Practice & Research. Clinical Gastroenterology|October 20, 2010
Inborn errors of carbohydrate metabolismErtan Mayatepek, Björn Hoffmann, Thomas Meissner
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 18, 2009
Neonatal pleural empyema in an extremely low birth weight infantKlaus Lohmeier, Ertan Mayatepek, Thomas Hoehn
Pharmacogenetics|November 27, 2004
Benzydamine metabolism in vivo is impaired in patients with deficiency of flavin-containing monooxygenase 3Ertan Mayatepek, Bianca Flock, Johannes Zschocke
European Journal of Pediatrics|October 9, 2009
Significant increase of succinylacetone within the first 12 h of life in hereditary tyrosinemia type 1Jan-Ulrich Schlump, Ertan Mayatepek, Ute Spiekerkoetter
Pageof 29