Korres S - Search Results

1

Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population.

Kokotas H, Van Laer L, Grigoriadou M, Iliadou V, Economides J, Pomoni S, Pampanos A, Eleftheriades N, Ferekidou E, Korres S, Giannoulia-Karantana A, Van Camp G, Petersen MB. Kokotas H, et al. Among authors: korres s. Am J Med Genet A. 2008 Nov 15;146A(22):2879-84. doi: 10.1002/ajmg.a.32546. Am J Med Genet A. 2008. PMID: 18925674

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. Among authors: korres gs, korres s. 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

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. Among authors: korres gs, korres s. 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.

4

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: korres gs, korres s. 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

5

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

6

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. Among authors: korres gs, korres s. Dis Markers. 2011;30(6):283-9. doi: 10.3233/DMA-2011-0786. Dis Markers. 2011. PMID: 21725156 Free PMC article.

7

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. Among authors: korres gs, korres s. 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.

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

Universal newborn hearing screening, a revolutionary diagnosis of deafness: real benefits and limitations.

Papacharalampous GX, Nikolopoulos TP, Davilis DI, Xenellis IE, Korres SG. Papacharalampous GX, et al. Eur Arch Otorhinolaryngol. 2011 Oct;268(10):1399-406. doi: 10.1007/s00405-011-1672-1. Epub 2011 Jun 23. Eur Arch Otorhinolaryngol. 2011. PMID: 21698417 Review.

10

Auditory neuropathy: endocochlear lesion or temporal processing impairment? Implications for diagnosis and management.

Vlastarakos PV, Nikolopoulos TP, Tavoulari E, Papacharalambous G, Korres S. Vlastarakos PV, et al. Among authors: korres s. Int J Pediatr Otorhinolaryngol. 2008 Aug;72(8):1135-50. doi: 10.1016/j.ijporl.2008.04.004. Epub 2008 May 27. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18502518 Review.

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