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Peripheral alpha-synuclein levels in patients with genetic and non-genetic forms of Parkinson's disease.
Emmanouilidou E, Papagiannakis N, Kouloulia S, Galaziou A, Antonellou R, Papadimitriou D, Athanasiadou A, Bozi M, Koros C, Maniati M, Vekrellis K, Ioannou PC, Stefanis L. Emmanouilidou E, et al. Among authors: maniati m. Parkinsonism Relat Disord. 2020 Apr;73:35-40. doi: 10.1016/j.parkreldis.2020.03.014. Epub 2020 Mar 22. Parkinsonism Relat Disord. 2020. PMID: 32234683
Genetic assessment of familial and early-onset Parkinson's disease in a Greek population.
Bozi M, Papadimitriou D, Antonellou R, Moraitou M, Maniati M, Vassilatis DK, Papageorgiou SG, Leonardos A, Tagaris G, Malamis G, Theofilopoulos D, Kamakari S, Stamboulis E, Hadjigeorgiou GM, Athanassiadou A, Michelakakis H, Papadimitriou A, Gasser T, Stefanis L. Bozi M, et al. Among authors: maniati m. Eur J Neurol. 2014 Jul;21(7):963-8. doi: 10.1111/ene.12315. Epub 2013 Dec 7. Eur J Neurol. 2014. PMID: 24313877
A Novel SNCA A30G Mutation Causes Familial Parkinson's Disease.
Liu H, Koros C, Strohäker T, Schulte C, Bozi M, Varvaresos S, Ibáñez de Opakua A, Simitsi AM, Bougea A, Voumvourakis K, Maniati M, Papageorgiou SG, Hauser AK, Becker S, Zweckstetter M, Stefanis L, Gasser T. Liu H, et al. Among authors: maniati m. Mov Disord. 2021 Jul;36(7):1624-1633. doi: 10.1002/mds.28534. Epub 2021 Feb 22. Mov Disord. 2021. PMID: 33617693
Nurr1 repression mediates cardinal features of Parkinson's disease in α-synuclein transgenic mice.
Argyrofthalmidou M, Spathis AD, Maniati M, Poula A, Katsianou MA, Sotiriou E, Manousaki M, Perier C, Papapanagiotou I, Papadopoulou-Daifoti Z, Pitychoutis PM, Alexakos P, Vila M, Stefanis L, Vassilatis DK. Argyrofthalmidou M, et al. Among authors: maniati m. Hum Mol Genet. 2021 Jul 28;30(16):1469-1483. doi: 10.1093/hmg/ddab118. Hum Mol Genet. 2021. PMID: 33902111 Free PMC article.
87 results