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Page 1
Motor and Nonmotor Features of Carriers of the p.A53T Alpha-Synuclein Mutation: A Longitudinal Study.
Papadimitriou D, Antonelou R, Miligkos M, Maniati M, Papagiannakis N, Bostantjopoulou S, Leonardos A, Koros C, Simitsi A, Papageorgiou SG, Kapaki E, Alcalay RN, Papadimitriou A, Athanassiadou A, Stamelou M, Stefanis L. Papadimitriou D, et al. Among authors: papadimitriou a. Mov Disord. 2016 Aug;31(8):1226-30. doi: 10.1002/mds.26615. Epub 2016 Mar 29. Mov Disord. 2016. PMID: 27028329
Distinct profiles of LRRK2 activation and Rab GTPase phosphorylation in clinical samples from different PD cohorts.
Petropoulou-Vathi L, Simitsi A, Valkimadi PE, Kedariti M, Dimitrakopoulos L, Koros C, Papadimitriou D, Papadimitriou A, Stefanis L, Alcalay RN, Rideout HJ. Petropoulou-Vathi L, et al. Among authors: papadimitriou d, papadimitriou a. NPJ Parkinsons Dis. 2022 Jun 8;8(1):73. doi: 10.1038/s41531-022-00336-5. NPJ Parkinsons Dis. 2022. PMID: 35676398 Free PMC article.
Positron emission tomography changes in PARK1 mutation.
Perani D, Garibotto V, Hadjigeorgiou GM, Papadimitriou D, Fazio F, Papadimitriou A. Perani D, et al. Among authors: papadimitriou d, papadimitriou a. Mov Disord. 2006 Jan;21(1):127-30. doi: 10.1002/mds.20691. Mov Disord. 2006. PMID: 16211612 No abstract available.
Lack of association of the UCHL-1 gene with Parkinson's disease in a Greek cohort: a haplotype-tagging approach.
Xiromerisiou G, Kyratzi E, Dardiotis E, Bozi M, Tsimourtou V, Stamboulis E, Ralli S, Vassilatis D, Gourbali V, Kountra PM, Fountas K, Papadimitriou A, Stefanis L, Hadjigeorgiou GM. Xiromerisiou G, et al. Among authors: papadimitriou a. Mov Disord. 2011 Aug 15;26(10):1955-7. doi: 10.1002/mds.23694. Epub 2011 May 28. Mov Disord. 2011. PMID: 21626562 No abstract available.
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.
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
Natalizumab-related progressive multifocal leukoencephalopathy in Greece.
Mitsikostas DD, Mastorodemos V, Tsagournizakis M, Kodounis A, Tsagkaropoulos A, Konitsiotis S, Toulas P, Papadimitriou A, Papadimitriou D, Tavernarakis A, Papadopoulos D. Mitsikostas DD, et al. Among authors: papadimitriou d, papadimitriou a. Mult Scler Relat Disord. 2014 Mar;3(2):203-10. doi: 10.1016/j.msard.2013.08.006. Epub 2013 Sep 24. Mult Scler Relat Disord. 2014. PMID: 25878008
323 results