KOMROWER COMMEMORATIVE LECTURES
| Year | Place | Speaker | Title |
| 2021 | |||
| 2020 | Virtual Meeting | Prof E Van Schaftingen | Elucidating the causes of metablic disorders: the new veins to explore |
| 2019 | Rotterdam | Dr C Vianey-Saban |
From fatty acid oxidation to riboflavin |
| 2018 | Athens | Prof P T Clayton | Restoring missing metabolites: from bile acid to B6 |
| 2016 | Rome | Prof M Zeviani | Mitochondrial Disorders, a journey through the magic circle and beyond |
| 2015 | Lyon | Prof B T Poll-The | Peroxisomal disorders and more…: Why I have not stopped examining patients |
| 2014 | Innsbruck | Prof G Brown | A wide circle around lactic acid |
| 2013 | Barcelona | Dr C Dionisi-Vici | The daily challenge of understanding and treating metabolic disorders in children |
| 2012 | Birmingham | Prof R J A Wanders | Inborn errors of metabolism including peroxisomal diseases in a changing world of omics and systems biology |
| 2011 | Geneva | Dr M T Vanier | Lysosomal neurolipidoses: the enigmas and the challenges |
| 2010 | Istanbul | Prof B Wilcken | Newborn Screening: How are we travelling? Where we might get to? |
| 2008 | Lisbon | Prof N Gregersen | Mitochondrial fatty acid oxidation defects, remaining challenges |
| 2007 | Hamburg | Prof W S Sly | Evolution of therapy for lysosomal diseases |
| 2005 | Paris | Prof J Leonard | The treatment of inborn errors of metabolism |
| 2004 | Amsterdam | Prof M Gibson | Gamma-hydroxybutyric aciduria: a biochemist’s education from a heritable disorder of GABA metabolism |
| 2002 | Dublin | Prof J Jaeken | Congenital disorders of glycosylation: its all in it |
| 2001 | Prague | Prof H Galjaard | New names for old disciplines |
| 1999 | Genova | Prof M Saudubray | Genetic hypoglycaemia |
| 1998 | York | Prof D Valle | Ornithine metabolism, metabolic network and normal biology |
| 1997 | Gothenburg | Prof S J Segal | Galactosaemia today: the enigma and the challenge |
| 1996 | Cardiff | Dr A M Spiegel | Inborn errors of signal transduction mutations in G Protein-coupled receptors as a cause of disease |
| 1995 | Toledo | Dr G Salem | Abnormal cholesterol biosynthesis in sitosterolaemia and the Smith-Lemli-Opitz syndrome |
| 1994 | Edinburgh | Prof H W Moser | Adrenoleukodystrophy, natural history, treatment and outcome |
| 1993 | Manchester | Prof J P Kraus | Molecular basis of phenotype expression in homocystinuria |