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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2005 2
2006 4
2007 1
2008 5
2009 2
2010 9
2011 6
2012 4
2013 2
2015 1
2022 1
2023 1
2024 0

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36 results

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Page 1
Age-related macular degeneration: genetic and clinical findings.
Kokotas H, Grigoriadou M, Petersen MB. Kokotas H, et al. Among authors: grigoriadou m. Clin Chem Lab Med. 2011 Apr;49(4):601-16. doi: 10.1515/CCLM.2011.091. Epub 2010 Dec 23. Clin Chem Lab Med. 2011. PMID: 21175380 Review.
Biomarkers in primary open angle glaucoma.
Kokotas H, Kroupis C, Chiras D, Grigoriadou M, Lamnissou K, Petersen MB, Kitsos G. Kokotas H, et al. Among authors: grigoriadou m. Clin Chem Lab Med. 2012 Dec;50(12):2107-19. doi: 10.1515/cclm-2012-0048. Clin Chem Lab Med. 2012. PMID: 22745021 Free article. Review.
Effectiveness of a Community-Based Crisis Resolution Team for Patients with Severe Mental Illness in Greece: A Prospective Observational Study.
Koureta A, Papageorgiou C, Asimopoulos C, Bismbiki E, Grigoriadou M, Xidia S, Papazafiri T, I Vlachos I, Margariti M. Koureta A, et al. Among authors: grigoriadou m. Community Ment Health J. 2023 Jan;59(1):14-24. doi: 10.1007/s10597-022-00983-1. Epub 2022 May 19. Community Ment Health J. 2023. PMID: 35588027 Free PMC article.
35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome.
Sarri C, Douzgou S, Kontos H, Anagnostopoulou K, Tümer Z, Grigoriadou M, Petersen MB, Kokotas H, Merou K, Pandelia E, Giouroukou E, Papanikolaou K, Côté GB, Gyftodimou Y. Sarri C, et al. Among authors: grigoriadou m. Cytogenet Genome Res. 2015;145(1):6-13. doi: 10.1159/000382046. Epub 2015 May 14. Cytogenet Genome Res. 2015. PMID: 25997743 Review.
Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
Sarri C, Douzgou S, Gyftodimou Y, Tümer Z, Ravn K, Pasparaki A, Sarafidou T, Kontos H, Kokotas H, Karadima G, Grigoriadou M, Pandelia E, Theodorou V, Moschonas NK, Petersen MB. Sarri C, et al. Among authors: grigoriadou m. Am J Med Genet A. 2011 Nov;155A(11):2841-54. doi: 10.1002/ajmg.a.34259. Epub 2011 Sep 30. Am J Med Genet A. 2011. PMID: 21964744 Review.
SLITRK6 mutations cause myopia and deafness in humans and mice.
Tekin M, Chioza BA, Matsumoto Y, Diaz-Horta O, Cross HE, Duman D, Kokotas H, Moore-Barton HL, Sakoori K, Ota M, Odaka YS, Foster J 2nd, Cengiz FB, Tokgoz-Yilmaz S, Tekeli O, Grigoriadou M, Petersen MB, Sreekantan-Nair A, Gurtz K, Xia XJ, Pandya A, Patton MA, Young JI, Aruga J, Crosby AH. Tekin M, et al. Among authors: grigoriadou m. J Clin Invest. 2013 May;123(5):2094-102. doi: 10.1172/JCI65853. Epub 2013 Apr 1. J Clin Invest. 2013. PMID: 23543054 Free PMC article.
A novel PIKFYVE mutation in fleck corneal dystrophy.
Kotoulas A, Kokotas H, Kopsidas K, Droutsas K, Grigoriadou M, Bajrami H, Schorderet DF, Petersen MB. Kotoulas A, et al. Among authors: grigoriadou m. Mol Vis. 2011;17:2776-81. Epub 2011 Oct 25. Mol Vis. 2011. PMID: 22065932 Free PMC article.
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss.
Kokotas H, Grigoriadou M, Yang L, Lodahl M, Rendtorff ND, Gyftodimou Y, Korres GS, Ferekidou E, Kandiloros D, Korres S, Tranebjærg L, Guan MX, Petersen MB. Kokotas H, et al. Among authors: grigoriadou m. Int J Pediatr Otorhinolaryngol. 2011 Jan;75(1):89-94. doi: 10.1016/j.ijporl.2010.10.016. Epub 2010 Nov 5. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21056478
36 results