Πλοήγηση ανά Συγγραφέα "Athanassiadou, A."
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Clinical phenotype in patients with α-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease
Papapetropoulos, S.; Paschalis, C.; Athanassiadou, A.; Papadimitriou, A.; Ellul, J.; Polymeropoulos, M. H.; Papapetropoulos, Th (2001)Objective - An Ala53Thr mutation of the α-synuclein gene has been recently identified as a rare cause of autosomal Parkinson's disease (PD). The clinical characteristics of 15 patients with PD living in Greece with the ... -
Genetic assessment of familial and early-onset Parkinson's disease in a Greek population
Bozi, M.; Papadimitriou, D.; Antonellou, R.; Moraitou, M.; Maniati, M.; Vassilatis, D. K.; Papageorgiou, S. G.; Leonardos, A.; Tagaris, G.; Malamis, G.; Theofilopoulos, D.; Kamakari, S.; Stamboulis, E.; Hadjigeorgiou, G. M.; Athanassiadou, A.; Michelakakis, H.; Papadimitriou, A.; Gasser, T.; Stefanis, L. (2014)Background and purpose Although the first mutation associated with Parkinson's disease (PD) was identified several years ago in the alpha-synuclein (SNCA) gene in families of Greek and Italian ancestry, a more systematic ... -
Glutathione S-transferase polymorphisms and onset age in alpha-synuclein A53T mutant Parkinson's disease
Golbe, L. I.; Di Iorio, G.; Markopoulou, K.; Athanassiadou, A.; Papapetropoulos, S.; Watts, R. L.; Vance, J. M.; Bonifati, V.; Williams, T. A.; Spychala, J. R.; Stenroos, E. S.; Johnson, W. G. (2007)Monogenic forms of Parkinson's disease (PD) provide an opportunity to examine mechanisms underlying phenotypic variation. Glutathione S-transferase (GST) has detoxification and antioxidative functions. To screen genetic ... -
Peripheral alpha-synuclein markers in subjects harboring the G209A mutation in the SNCA gene
Emmanouilidou, E.; Antonelou, R.; Papadimitriou, D.; Maniati, M.; Papagiannakis, N.; Stamelou, M.; Tagaris, G.; Papageorgiou, S.; Kapaki, E.; Leonardos, N.; Ioannou, P.; Bostantjopoulou, S.; Papadimitriou, A.; Athanassiadou, A.; Vekrellis, K.; Stefanis, L. (2014) -
Phenotypic spectrum of SNCA G209A mutation carriers for familial Parkinson's disease in Greece
Papadimitriou, D.; Antonelou, R.; Stamelou, M.; Bozi, M.; Maniati, M.; Papagiannakis, N.; Bostantjopoulou, S.; Leonardos, A.; Papageorgiou, S.; Hadjigeorgiou, G.; Kapaki, E.; Tagaris, G.; Papadimitriou, A.; Athanassiadou, A.; Stefanis, L. (2014)