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European Neurology|December 20, 2011
Late onset glycogen storage disease type II: pitfalls in the diagnosisG K Papadimas, K Spengos, C Papadopoulos, et al.Molecular Genetics and Metabolism Reports|December 2, 2016
Highlighting intrafamilial clinical heterogeneity in late-onset Pompe diseaseC Papadopoulos, G K Papadimas, H Michelakakis, et al.The International Journal of Neuroscience|May 23, 2015
Electrodiagnosis and muscle biopsy in asymptomatic hyperckemiaP Kokotis, G K Papadimas, V Zouvelou, et al.Journal of Neuromuscular Diseases|November 18, 2016
GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation PathologyG K Papadimas, A Evilä, C Papadopoulos, et al.Eye (London, England)|December 9, 2017
Early onset posterior subscapular cataract in a series of myotonic dystrophy type 2 patientsC Papadopoulos, K Kekou, S Xirou, et al.The Neurologist|May 12, 2009
Superficial siderosis of central nervous system mimicking multiple sclerosisG K Papadimas, M Rentzos, V Zouvelou, et al.Molecular Genetics and Metabolism Reports|March 5, 2021
Aldolase A deficiency: Report of new cases and literature reviewC Papadopoulos, M Svingou, K Kekou, et al.Clinical Neurology and Neurosurgery|January 11, 2011
Adult Pompe disease: clinical manifestations and outcome of the first Greek patients receiving enzyme replacement therapyG K Papadimas, K Spengos, A Konstantinopoulou, et al.Molecular Genetics and Metabolism|October 8, 2010
Body composition analysis in late-onset Pompe diseaseG K Papadimas, G Terzis, S Methenitis, et al.Archives of Toxicology|July 5, 2005
Platelet-activating factor (PAF) involvement in acetaminophen-induced liver toxicity and regenerationA D Grypioti, S E Theocharis, G K Papadimas, et al.Pageof 1