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Best Practice & Research. Clinical Gastroenterology|October 20, 2010
Inborn errors of carbohydrate metabolismErtan Mayatepek, Björn Hoffmann, Thomas Meissner
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
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
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 18, 2004
Urinary alpha-ketoglutarate is elevated in patients with hyperinsulinism-hyperammonemia syndromeThomas Meissner, Ertan Mayatepek, Martina Kinner, et al.
Medizinische Klinik (Munich, Germany : 1983)|October 13, 2005
[Situation of adult patients with inborn errors of metabolism. A survey in Germany]Björn Hoffmann, Martin Schwarz, Dieter Häussinger, et al.
Journal of Inherited Metabolic Disease|August 10, 2010
Simultaneous LC-MS/MS determination of phenylbutyrate, phenylacetate benzoate and their corresponding metabolites phenylacetylglutamine and hippurate in blood and urineMaurice D Laryea, Diran Herebian, Thomas Meissner, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2026
Physiology and diagnostic potential of beta-hydroxybutyrate in neonatal glycemia - a prospective cohort studyHenrike Hoermann, Ertan Mayatepek, Thomas Meissner, et al.
European Journal of Endocrinology|June 26, 2003
Long-term follow-up of 114 patients with congenital hyperinsulinismThomas Meissner, Udo Wendel, Peter Burgard, et al.
Biochemical and Biophysical Research Communications|June 11, 2002
Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienesSacha Ferdinandusse, Thomas Meissner, Ronald J A Wanders, et al.
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