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Page 1
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: ralli s. Neurol Sci. 2019 Feb;40(2):253-260. doi: 10.1007/s10072-018-3617-6. Epub 2018 Oct 26. Neurol Sci. 2019. PMID: 30361804
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. Among authors: ralli s. 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
Teaching NeuroImages: Isolated bilateral trigeminal nerve palsy.
Dardiotis E, Patramani G, Ralli S, Hadjigeorgiou GM. Dardiotis E, et al. Among authors: ralli s. Neurology. 2011 Jun 14;76(24):e115. doi: 10.1212/WNL.0b013e31821f4622. Neurology. 2011. PMID: 21670430 No abstract available.
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: ralli s. 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.
Images in clinical medicine. Paraneoplastic neuromyotonia.
Dardiotis E, Ralli S. Dardiotis E, et al. Among authors: ralli s. N Engl J Med. 2015 Apr 30;372(18):e24. doi: 10.1056/NEJMicm1402098. N Engl J Med. 2015. PMID: 25923574 Free article. No abstract available.
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.
Mitropoulos K, Merkouri Papadima E, Xiromerisiou G, Balasopoulou A, Charalampidou K, Galani V, Zafeiri KV, Dardiotis E, Ralli S, Deretzi G, John A, Kydonopoulou K, Papadopoulou E, di Pardo A, Akcimen F, Loizedda A, Dobričić V, Novaković I, Kostić VS, Mizzi C, Peters BA, Basak N, Orrù S, Kiskinis E, Cooper DN, Gerou S, Drmanac R, Bartsakoulia M, Tsermpini EE, Hadjigeorgiou GM, Ali BR, Katsila T, Patrinos GP. Mitropoulos K, et al. Among authors: ralli s. Hum Genomics. 2017 Dec 8;11(1):30. doi: 10.1186/s40246-017-0126-2. Hum Genomics. 2017. PMID: 29216901 Free PMC article.
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.
Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage S, Lin JJ, Lynch T, Mellick GD, de Nigris F, Opala G, Prigione A, Quattrone A, Ross OA, Satake W, Silburn PA, Tan EK, Toda T, Tomiyama H, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Maraganore DM; Genetic Epidemiology of Parkinson's disease consortium. Krüger R, et al. Neurobiol Aging. 2011 Mar;32(3):548.e9-18. doi: 10.1016/j.neurobiolaging.2009.11.021. Epub 2009 Dec 24. Neurobiol Aging. 2011. PMID: 20036034 Free PMC article.
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: ralli s. 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.
33 results