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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
Best Practice & Research. Clinical Gastroenterology|October 20, 2010
Inborn errors of carbohydrate metabolismErtan Mayatepek, Björn Hoffmann, Thomas Meissner
Frontiers in Endocrinology|June 26, 2023
Neonatal hypoglycemia: lack of evidence for a safe managementMarcia Roeper, Henrike Hoermann, Sebastian Kummer, et al.
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.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 2004
Analysis of cysteinyl leukotrienes and their metabolites in bile of patients with peroxisomal or mitochondrial beta-oxidation defectsErtan Mayatepek, Sacha Ferdinandusse, Thomas Meissner, et al.
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