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Page 1
Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS.
Sokratous M, Lucia S, Bourinaris T, Marogianni C, Arnaoutoglou M, Patrikiou E, Ralli S, Markou A, Dardiotis E, Houlden H, Hadjigeorgiou GM, Xiromerisiou G. Sokratous M, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2020 Aug;21(5-6):470-472. doi: 10.1080/21678421.2020.1757115. Epub 2020 Apr 26. Amyotroph Lateral Scler Frontotemporal Degener. 2020. PMID: 32338076
Genetic polymorphisms in amyotrophic lateral sclerosis: Evidence for implication in detoxification pathways of environmental toxicants.
Dardiotis E, Siokas V, Sokratous M, Tsouris Z, Michalopoulou A, Andravizou A, Dastamani M, Ralli S, Vinceti M, Tsatsakis A, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: sokratous m. Environ Int. 2018 Jul;116:122-135. doi: 10.1016/j.envint.2018.04.008. Epub 2018 Apr 17. Environ Int. 2018. PMID: 29677557 Free article. Review. No abstract available.
AQP4 tag SNPs in patients with intracerebral hemorrhage in Greek and Polish population.
Dardiotis E, Siokas V, Marogianni C, Aloizou AM, Sokratous M, Paterakis K, Dardioti M, Grigoriadis S, Brotis A, Kapsalaki E, Fountas K, Jagiella J, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: sokratous m. Neurosci Lett. 2019 Mar 23;696:156-161. doi: 10.1016/j.neulet.2018.12.025. Epub 2018 Dec 19. Neurosci Lett. 2019. PMID: 30578930
Body mass index in patients with Multiple Sclerosis: a meta-analysis.
Dardiotis E, Tsouris Z, Aslanidou P, Aloizou AM, Sokratous M, Provatas A, Siokas V, Deretzi G, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: sokratous m. Neurol Res. 2019 Sep;41(9):836-846. doi: 10.1080/01616412.2019.1622873. Epub 2019 May 31. Neurol Res. 2019. PMID: 31146649
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited: Genotype-phenotype correlations of all published cases.
Xiromerisiou G, Marogianni C, Dadouli K, Zompola C, Georgouli D, Provatas A, Theodorou A, Zervas P, Nikolaidou C, Stergiou S, Ntellas P, Sokratous M, Stathis P, Paraskevas GP, Bonakis A, Voumvourakis K, Hadjichristodoulou C, Hadjigeorgiou GM, Tsivgoulis G. Xiromerisiou G, et al. Among authors: sokratous m. Neurol Genet. 2020 May 11;6(3):e434. doi: 10.1212/NXG.0000000000000434. eCollection 2020 Jun. Neurol Genet. 2020. PMID: 32582863 Free PMC article. Review.
CpG Island Methylation Patterns in Relapsing-Remitting Multiple Sclerosis.
Sokratous M, Dardiotis E, Bellou E, Tsouris Z, Michalopoulou A, Dardioti M, Siokas V, Rikos D, Tsatsakis A, Kovatsi L, Bogdanos DP, Hadjigeorgiou GM. Sokratous M, et al. J Mol Neurosci. 2018 Mar;64(3):478-484. doi: 10.1007/s12031-018-1046-x. Epub 2018 Mar 7. J Mol Neurosci. 2018. PMID: 29516350
α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism.
Sokratous M, Breza M, Senkevich K, Gan-Or Z, Kalampokini S, Spanaki C, Provatas A, Zaunmuktane Z, Valotassiou V, Georgoulias P, Efthymiou S, Hadjigeorgiou GM, Houlden H, Xiromerisiou G. Sokratous M, et al. Mov Disord. 2021 Sep;36(9):2209-2212. doi: 10.1002/mds.28735. Mov Disord. 2021. PMID: 34543462 No abstract available.
18 results