Sfoglia per Autore "Singleton, A."
Items 1-5 di 5
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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) -
Association of α-synuclein Rep1 polymorphism and Parkinson's disease: Influence of Rep1 on age at onset
Hadjigeorgiou, G. H.; Xiromerisiou, G.; Gourbali, V.; Aggelakis, K.; Scarmeas, N.; Papadimitriou, A.; Singleton, A. (2006)The α-synuclein Rep1 polymorphism was studied in patients and controls in an ethnic Greek population. There was an association of allele 2 with risk of Parkinson's disease (PD; adjusted odd ratio = 3.25; 95% CI = 1.80-5.87). ... -
BDNF haplotype tagging SNPs in Greek sporadic PD patients and patterns of linkage disequilibrium
Xiromerisiou, G.; Tsimourtou, V.; Gourbali, V.; Aggelakis, K.; Dardiotis, E.; Dardioti, M.; Noulas, G.; Papadimitriou, A.; Singleton, A.; Hadjigeorgiou, G. (2006) -
How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the disease
Cookson, M. R.; Xiromerisiou, G.; Singleton, A. (2005)Purpose of review Rapid progress in genetics has meant that there are now five genes identified for 'Parkinson's disease'. The detailed phenotypes vary, but generally the dominant genes cause a Lewy body disease spectrum ... -
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant PD: identification of two novel LRRK2 variants
Yiromerisiou, G.; Gourbali, V.; Dardiotis, E.; Dardioti, M.; Tsimourtou, V.; Aggelakis, K.; Papakonstaninou, I.; Noulas, G.; Papadimitriou, A.; Singleton, A.; Hadjigeorgiou, G. (2006)