Rikos D - Search Results

1

A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases.

Xiromerisiou G, Dadouli K, Marogianni C, Provatas A, Ntellas P, Rikos D, Stathis P, Georgouli D, Loules G, Zamanakou M, Hadjigeorgiou GM. Xiromerisiou G, et al. Among authors: rikos d. J Mol Neurosci. 2020 Jan;70(1):131-141. doi: 10.1007/s12031-019-01410-z. Epub 2019 Nov 7. J Mol Neurosci. 2020. PMID: 31701440 Review.

2

Reporting quality of randomized-controlled trials in multiple sclerosis from 2000 to 2015, based on CONSORT statement.

Rikos D, Dardiotis E, Tsivgoulis G, Zintzaras E, Hadjigeorgiou GM. Rikos D, et al. Mult Scler Relat Disord. 2016 Sep;9:135-9. doi: 10.1016/j.msard.2016.07.013. Epub 2016 Jul 27. Mult Scler Relat Disord. 2016. PMID: 27645361

3

The Role of TOR1A Polymorphisms in Dystonia: A Systematic Review and Meta-Analysis.

Siokas V, Dardiotis E, Tsironi EE, Tsivgoulis G, Rikos D, Sokratous M, Koutsias S, Paterakis K, Deretzi G, Hadjigeorgiou GM. Siokas V, et al. Among authors: rikos d. PLoS One. 2017 Jan 12;12(1):e0169934. doi: 10.1371/journal.pone.0169934. eCollection 2017. PLoS One. 2017. PMID: 28081261 Free PMC article. Review.

4

A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature.

Dardiotis E, Siokas V, Pantazi E, Dardioti M, Rikos D, Xiromerisiou G, Markou A, Papadimitriou D, Speletas M, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: rikos d. Neurobiol Aging. 2017 May;53:194.e13-194.e22. doi: 10.1016/j.neurobiolaging.2017.01.015. Epub 2017 Jan 20. Neurobiol Aging. 2017. PMID: 28214109 Review.

5

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. Among authors: rikos d. 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

6

Replication study of GWAS risk loci in Greek multiple sclerosis patients.

Hadjigeorgiou GM, Kountra PM, Koutsis G, Tsimourtou V, Siokas V, Dardioti M, Rikos D, Marogianni C, Aloizou AM, Karadima G, Ralli S, Grigoriadis N, Bogdanos D, Panas M, Dardiotis E. Hadjigeorgiou GM, et al. Among authors: rikos d. Neurol Sci. 2019 Feb;40(2):253-260. doi: 10.1007/s10072-018-3617-6. Epub 2018 Oct 26. Neurol Sci. 2019. PMID: 30361804

7

ERCC6L2 rs591486 polymorphism and risk for amyotrophic lateral sclerosis in Greek population.

Dardiotis E, Karampinis E, Siokas V, Aloizou AM, Rikos D, Ralli S, Papadimitriou D, Bogdanos DP, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: rikos d. Neurol Sci. 2019 Jun;40(6):1237-1244. doi: 10.1007/s10072-019-03825-3. Epub 2019 Mar 16. Neurol Sci. 2019. PMID: 30879219

8

The role of C9orf72 in neurodegenerative disorders: a systematic review, an updated meta-analysis, and the creation of an online database.

Marogianni C, Rikos D, Provatas A, Dadouli K, Ntellas P, Tsitsi P, Patrinos G, Dardiotis E, Hadjigeorgiou G, Xiromerisiou G. Marogianni C, et al. Among authors: rikos d. Neurobiol Aging. 2019 Dec;84:238.e25-238.e34. doi: 10.1016/j.neurobiolaging.2019.04.012. Epub 2019 Apr 24. Neurobiol Aging. 2019. PMID: 31126629

9

TREM2 R47H (rs75932628) variant is unlikely to contribute to Multiple Sclerosis susceptibility and severity in a large Greek MS cohort.

Rikos D, Siokas V, Aloizou AM, Tsouris Z, Aslanidou P, Koutsis G, Anagnostouli M, Bogdanos DP, Grigoriadis N, Hadjigeorgiou GM, Dardiotis E. Rikos D, et al. Mult Scler Relat Disord. 2019 Oct;35:116-118. doi: 10.1016/j.msard.2019.07.007. Epub 2019 Jul 20. Mult Scler Relat Disord. 2019. PMID: 31362167

10

Reporting Quality of Randomized Controlled Trials in Restless Legs Syndrome Based on the CONSORT Statement.

Rikos D, Dardiotis E, Aloizou AM, Siokas V, Zintzaras E, Hadjigeorgiou GM. Rikos D, et al. Tremor Other Hyperkinet Mov (N Y). 2019 Jun 18;9. doi: 10.7916/d8-0f2v-aq62. eCollection 2019. Tremor Other Hyperkinet Mov (N Y). 2019. PMID: 31413890 Free PMC article.

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