Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Zafeiriou, DI*" or (type exact bookEditor and editor="Zafeiriou, DI*") Add to list Journal Article A2 open access Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene George K. Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, Rudy Van Coster (UGent) , Joél Smet (UGent) , Sara Seneca, Constantinos Papadopoulos, Evangelia Kararizou and Dimitrios Zafeiriou (2020) ACTA MYOLOGICA (TESTO STAMPATO). 39(2). p.94-97 Add to list Conference Paper C3 Succinyl-CoA ligase deficiency : report on the first patient resulting from a combined defect in SUGL1 an SUGL2 genes DI Zafeiriou, S Batzios, E Vargiami, M Willemsen, E Morava, L Van den Heuvel, Joél Smet (UGent) , Rudy Van Coster (UGent) , S Seneca, R Wanders, et al. (2013) EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 17(suppl. 1). p.S6-S7 Add to list Journal Article A1 Ethylmalonic encephalopathy: Clinical and biochemical observations DI ZAFEIRIOU, P AUGOUSTIDES-SAVVOPOULOU, D HAAS, Joél Smet (UGent) , P TRIANTAFYLOU, E VARGIAMI, M TARNIOLAKI, N GORNBAKIS, Rudy Van Coster (UGent) , AC SEWELL, et al. (2007) NEUROPEDIATRICS. 38(2). p.78-82