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Autoantibodies to alpha-synuclein in inherited Parkinson's disease.
Papachroni KK, Ninkina N, Papapanagiotou A, Hadjigeorgiou GM, Xiromerisiou G, Papadimitriou A, Kalofoutis A, Buchman VL. Papachroni KK, et al. Among authors: papadimitriou a. J Neurochem. 2007 May;101(3):749-56. doi: 10.1111/j.1471-4159.2006.04365.x. J Neurochem. 2007. PMID: 17448146 Free PMC article.
Association between AKT1 gene and Parkinson's disease: a protective haplotype.
Xiromerisiou G, Hadjigeorgiou GM, Papadimitriou A, Katsarogiannis E, Gourbali V, Singleton AB. Xiromerisiou G, et al. Among authors: papadimitriou a. Neurosci Lett. 2008 May 9;436(2):232-4. doi: 10.1016/j.neulet.2008.03.026. Epub 2008 Mar 15. Neurosci Lett. 2008. PMID: 18395980 Free PMC article.
The cortical excitability profile of patients with the G209A SNCA mutation versus patients with sporadic Parkinson's disease: A transcranial magnetic stimulation study.
Kimiskidis VK, Papayiannopoulos S, Sotirakoglou K, Karakasis H, Katsarou Z, Kazis DA, Papaliagkas V, Gatzonis S, Papadimitriou A, Hadjigeorgiou G, Bostanjopoulou S. Kimiskidis VK, et al. Among authors: papadimitriou a. Neurophysiol Clin. 2018 Sep;48(4):203-206. doi: 10.1016/j.neucli.2018.04.002. Epub 2018 May 3. Neurophysiol Clin. 2018. PMID: 29729894
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.
Scholz SW, Xiromerisiou G, Fung HC, Eerola J, Hellström O, Papadimitriou A, Hadjigeorgiou GM, Tienari PJ, Fernandez HH, Mandel R, Okun MS, Gwinn-Hardy K, Singleton AB. Scholz SW, et al. Among authors: papadimitriou a. Neurosci Lett. 2006 Mar 13;395(3):227-9. doi: 10.1016/j.neulet.2005.10.081. Epub 2005 Nov 18. Neurosci Lett. 2006. PMID: 16298483
321 results