Πλοήγηση ανά Συγγραφέα "Stamelou, M."

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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)
THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations

Xiromerisiou, G.; Houlden, H.; Scarmeas, N.; Stamelou, M.; Kara, E.; Hardy, J.; Lees, A. J.; Korlipara, P.; Limousin, P.; Paudel, R.; Hadjigeorgiou, G. M.; Bhatia, K. P. (2012)

THAP1 mutations have been shown to be the cause of DYT6. A number of different mutation types and locations in the THAP1 gene have been associated with a range of severity and dystonia phenotypes, but, as yet, it has been ...