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

Year Number of Results
2004 1
2007 2
2010 1
2013 2
2014 1
2015 2
2016 4
2017 3
2020 1
2021 2
2022 4
2023 2
2024 0

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21 results

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Page 1
Phenotype-driven variant filtration strategy in exome sequencing toward a high diagnostic yield and identification of 85 novel variants in 400 patients with rare Mendelian disorders.
Marinakis NM, Svingou M, Veltra D, Kekou K, Sofocleous C, Tilemis FN, Kosma K, Tsoutsou E, Fryssira H, Traeger-Synodinos J. Marinakis NM, et al. Among authors: kekou k. Am J Med Genet A. 2021 Aug;185(8):2561-2571. doi: 10.1002/ajmg.a.62338. Epub 2021 May 19. Am J Med Genet A. 2021. PMID: 34008892
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
Bladen CL, Salgado D, Monges S, Foncuberta ME, Kekou K, Kosma K, Dawkins H, Lamont L, Roy AJ, Chamova T, Guergueltcheva V, Chan S, Korngut L, Campbell C, Dai Y, Wang J, Barišić N, Brabec P, Lahdetie J, Walter MC, Schreiber-Katz O, Karcagi V, Garami M, Viswanathan V, Bayat F, Buccella F, Kimura E, Koeks Z, van den Bergen JC, Rodrigues M, Roxburgh R, Lusakowska A, Kostera-Pruszczyk A, Zimowski J, Santos R, Neagu E, Artemieva S, Rasic VM, Vojinovic D, Posada M, Bloetzer C, Jeannet PY, Joncourt F, Díaz-Manera J, Gallardo E, Karaduman AA, Topaloğlu H, El Sherif R, Stringer A, Shatillo AV, Martin AS, Peay HL, Bellgard MI, Kirschner J, Flanigan KM, Straub V, Bushby K, Verschuuren J, Aartsma-Rus A, Béroud C, Lochmüller H. Bladen CL, et al. Among authors: kekou k. Hum Mutat. 2015 Apr;36(4):395-402. doi: 10.1002/humu.22758. Epub 2015 Mar 17. Hum Mutat. 2015. PMID: 25604253 Free PMC article.
Caveolinopathies in Greece.
Papadopoulos C, Papadimas GK, Kekou K, Spengos K, Svigou M, Kitsiou-Tzeli S, Manta P. Papadopoulos C, et al. Among authors: kekou k. Neurologist. 2015 Jul;20(1):8-12. doi: 10.1097/NRL.0000000000000036. Neurologist. 2015. PMID: 26185955
A Greek National Cross-Sectional Study on Myotonic Dystrophies.
Papadimas GK, Papadopoulos C, Kekou K, Kartanou C, Kladi A, Nitsa E, Sofocleous C, Tsanou E, Sarmas I, Kaninia S, Chroni E, Tsivgoulis G, Kimiskidis V, Arnaoutoglou M, Stefanis L, Panas M, Koutsis G, Karadima G, Traeger-Synodinos J. Papadimas GK, et al. Among authors: kekou k. Int J Mol Sci. 2022 Dec 7;23(24):15507. doi: 10.3390/ijms232415507. Int J Mol Sci. 2022. PMID: 36555146 Free PMC article.
Myotonic dystrophy type 2 presenting as inflammatory myopathy.
Papadopoulos C, Panagopoulos G, Kekou K, Fardis V, Kitsiou-Tzeli S, Papadimas GK. Papadopoulos C, et al. Among authors: kekou k. Neurol India. 2016 Sep-Oct;64(5):1051-2. doi: 10.4103/0028-3886.190276. Neurol India. 2016. PMID: 27625258 Free article. No abstract available.
Author's Reply: Myotonic dystrophy: The occurrence of early-onset cataract.
Papadopoulos C, Panagopoulos G, Kekou K, Fardis V, Kitsiou-Tzeli S, Papadimas GK. Papadopoulos C, et al. Among authors: kekou k. Neurol India. 2017 Jul-Aug;65(4):923. doi: 10.4103/neuroindia.NI_481_17. Neurol India. 2017. PMID: 28681796 Free article. No abstract available.
A simplified approach for FSHD molecular testing.
Papanikos F, Skoulatou C, Sakellariou P, Kekou K, Christopoulos TK, Kanavakis E, Traeger-Synodinos J, Ioannou PC. Papanikos F, et al. Among authors: kekou k. Clin Chim Acta. 2014 Feb 15;429:96-103. doi: 10.1016/j.cca.2013.11.032. Epub 2013 Dec 7. Clin Chim Acta. 2014. PMID: 24321734
21 results