Grigoriadou M - Search Results

1

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: grigoriadou m. 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.

2

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: grigoriadou m. 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

3

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: grigoriadou m. 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

4

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: grigoriadou m. 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

5

Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.

Kokotas H, Grigoriadou M, Hatzaki A, Antoniadi T, Giannoulia-Karantana A, Petersen MB. Kokotas H, et al. Among authors: grigoriadou m. Genet Test Mol Biomarkers. 2010 Apr;14(2):189-92. doi: 10.1089/gtmb.2009.0136. Genet Test Mol Biomarkers. 2010. PMID: 20059378

6

Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?

Kokotas H, Grigoriadou M, Villamar M, Giannoulia-Karantana A, del Castillo I, Petersen MB. Kokotas H, et al. Among authors: grigoriadou m. Genet Test Mol Biomarkers. 2010 Apr;14(2):183-7. doi: 10.1089/gtmb.2009.0146. Genet Test Mol Biomarkers. 2010. PMID: 20073550

7

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

8

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: grigoriadou m. Dis Markers. 2011;30(6):283-9. doi: 10.3233/DMA-2011-0786. Dis Markers. 2011. PMID: 21725156 Free PMC article.

9

Compound heterozygosity of the novel c.292C>T (p.R98W) and the c.35delG GJB2 mutations in postlingual, non-syndromic, sensorineural deafness.

Petersen MB, Grigoriadou M, Economides J, Kokotas H. Petersen MB, et al. Among authors: grigoriadou m. Int J Pediatr Otorhinolaryngol. 2012 Apr;76(4):549-51. doi: 10.1016/j.ijporl.2012.01.014. Epub 2012 Feb 8. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22321824

10

The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness.

Petersen MB, Grigoriadou M, Koutroumpe M, Kokotas H. Petersen MB, et al. Among authors: grigoriadou m. Int J Pediatr Otorhinolaryngol. 2012 Jul;76(7):969-71. doi: 10.1016/j.ijporl.2012.03.007. Epub 2012 Apr 6. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22484064

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