Auflistung nach Autor "Papakonstantinou, I."
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Association of alpha-synuclein Rep1 polymorphism with risk for Parkinson's disease and influence on age at onset of Parkinson's disease
Xiromerisiou, G.; Gourbali, V.; Aggelakis, K.; Dardiotis, E.; Tsimourtou, V.; Papadimitriou, A.; Papakonstantinou, I.; Scarmeas, N.; Singleton, A.; Hadjigeorgiou, G. (2005) -
Paraoxonase 1 (PON1) gene polyrnoprhism (M55I) and Parkinson's disease
Xiromerissiou, G.; Gourbali, V.; Aggelakis, K.; Dardiotis, E.; Bakouras, S.; Papakonstantinou, I.; Kiriakakis, V.; Papadirnitrioul, A.; Hadjigeorgiou, G. M. (2004) -
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants
Xiromerisiou, G.; Hadjigeorgiou, G. M.; Gourbali, V.; Johnson, J.; Papakonstantinou, I.; Papadimitriou, A.; Singleton, A. B. (2007)Mutations in SNCA and LRRK2 genes, encoding alpha-synuclein and leucine-rich repeat kinase 2, respectively, cause autosomal dominant Parkinson's disease (AdPD). The LRRK2 G2019S (c.6055G > A) and R1441G (c.4321C > G) ...