Korres G - Search Results

1

Genetic origins of the Minoans and Mycenaeans.

Lazaridis I, Mittnik A, Patterson N, Mallick S, Rohland N, Pfrengle S, Furtwängler A, Peltzer A, Posth C, Vasilakis A, McGeorge PJP, Konsolaki-Yannopoulou E, Korres G, Martlew H, Michalodimitrakis M, Özsait M, Özsait N, Papathanasiou A, Richards M, Roodenberg SA, Tzedakis Y, Arnott R, Fernandes DM, Hughey JR, Lotakis DM, Navas PA, Maniatis Y, Stamatoyannopoulos JA, Stewardson K, Stockhammer P, Pinhasi R, Reich D, Krause J, Stamatoyannopoulos G. Lazaridis I, et al. Among authors: korres g. Nature. 2017 Aug 10;548(7666):214-218. doi: 10.1038/nature23310. Epub 2017 Aug 2. Nature. 2017. PMID: 28783727 Free PMC article.

2

The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Papadopoulou E, Neou P, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB. Kokotas H, et al. Biochem Biophys Res Commun. 2009 Dec 18;390(3):755-7. doi: 10.1016/j.bbrc.2009.10.044. Epub 2009 Oct 14. Biochem Biophys Res Commun. 2009. PMID: 19835846

3

Detection of deafness-causing mutations in the Greek mitochondrial genome.

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Kandiloros D, Korres S, Petersen MB. Kokotas H, et al. Dis Markers. 2011;30(6):283-9. doi: 10.3233/DMA-2011-0786. Dis Markers. 2011. PMID: 21725156 Free PMC article.

4

Sudden hearing loss in a family with GJB2 related progressive deafness.

Kokotas H, Theodosiou M, Korres G, Grigoriadou M, Ferekidou E, Giannoulia-Karantana A, Petersen MB, Korres S. Kokotas H, et al. Among authors: korres g, korres s. Int J Pediatr Otorhinolaryngol. 2008 Nov;72(11):1735-40. doi: 10.1016/j.ijporl.2008.08.006. Epub 2008 Sep 21. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18809215

5

Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Giannoulia-Karantana A, Kandiloros D, Korres S, Petersen MB. Kokotas H, et al. J Hum Genet. 2010 May;55(5):265-9. doi: 10.1038/jhg.2010.23. Epub 2010 Mar 19. J Hum Genet. 2010. PMID: 20300122 Review.

6

Screening of a Greek deafness population for the A7445G mitochondrial DNA mutation.

Kokotas H, Grigoriadou M, Korres GS, Ferekidou E, Kandiloros D, Korres S, Petersen MB. Kokotas H, et al. Mol Genet Metab. 2010 Jul;100(3):300-1. doi: 10.1016/j.ymgme.2010.03.016. Epub 2010 Mar 23. Mol Genet Metab. 2010. PMID: 20382059 No abstract available.

7

Making universal newborn hearing screening a success.

Korres SG, Balatsouras DG, Nikolopoulos T, Korres GS, Ferekidis E. Korres SG, et al. Among authors: korres gs. Int J Pediatr Otorhinolaryngol. 2006 Feb;70(2):241-6. doi: 10.1016/j.ijporl.2005.06.010. Epub 2005 Jul 18. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16029898

8

Distortion product otoacoustic emissions in an industrial setting.

Korres GS, Balatsouras DG, Tzagaroulakis A, Kandiloros D, Ferekidou E, Korres S. Korres GS, et al. Among authors: korres s. Noise Health. 2009 Apr-Jun;11(43):103-10. doi: 10.4103/1463-1741.50695. Noise Health. 2009. PMID: 19414930

9

Screening protocols for the prevention of occupational noise-induced hearing loss: the role of conventional and extended high frequency audiometry may vary according to the years of employment.

Riga M, Korres G, Balatsouras D, Korres S. Riga M, et al. Among authors: korres g, korres s. Med Sci Monit. 2010 Jul;16(7):CR352-6. doi: 10.12659/msm.880932. Med Sci Monit. 2010. PMID: 20581779

10

The effect of very low birth weight on otoacoustic emissions.

Korres SG, Balatsouras DG, Gkoritsa E, Kandiloros D, Korres GS, Ferekidis E. Korres SG, et al. Among authors: korres gs. B-ENT. 2007;3(1):15-20. B-ENT. 2007. PMID: 17451121

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