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54 results

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Page 1
Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree.
Iliadou V, Van Den Bogaert K, Eleftheriades N, Aperis G, Vanderstraeten K, Fransen E, Thys M, Grigoriadou M, Pampanos A, Economides J, Iliades T, Van Camp G, Petersen MB. Iliadou V, et al. Among authors: grigoriadou m. Int J Pediatr Otorhinolaryngol. 2006 Apr;70(4):631-7. doi: 10.1016/j.ijporl.2005.08.012. Epub 2005 Sep 15. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16168495
Prevalence of GJB2 mutations in prelingual deafness in the Greek population.
Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB. Pampanos A, et al. Among authors: grigoriadou m. Int J Pediatr Otorhinolaryngol. 2002 Sep 2;65(2):101-8. doi: 10.1016/s0165-5876(02)00177-5. Int J Pediatr Otorhinolaryngol. 2002. PMID: 12176179
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1.
Thys M, Van Den Bogaert K, Iliadou V, Vanderstraeten K, Dieltjens N, Schrauwen I, Chen W, Eleftheriades N, Grigoriadou M, Pauw RJ, Cremers CR, Smith RJ, Petersen MB, Van Camp G. Thys M, et al. Among authors: grigoriadou m. Eur J Hum Genet. 2007 Mar;15(3):362-8. doi: 10.1038/sj.ejhg.5201761. Epub 2007 Jan 10. Eur J Hum Genet. 2007. PMID: 17213839
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
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
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
Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.
Iliades T, Eleftheriades N, Iliadou V, Pampanos A, Voyiatzis N, Economides J, Leotsakos P, Neou P, Tsakanikos M, Antoniadi T, Konstantopoulou I, Yannoukakos D, Grigoriadou M, Skevas A, Petersen MB. Iliades T, et al. Among authors: grigoriadou m. ORL J Otorhinolaryngol Relat Spec. 2002 Sep-Oct;64(5):321-3. doi: 10.1159/000066088. ORL J Otorhinolaryngol Relat Spec. 2002. PMID: 12417772
Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece.
Iliadou V, Eleftheriades N, Metaxas AS, Skevas A, Kiratzidis T, Pampanos A, Voyiatzis N, Grigoriadou M, Petersen MB, Iliades T. Iliadou V, et al. Among authors: grigoriadou m. Eur Arch Otorhinolaryngol. 2004 May;261(5):259-61. doi: 10.1007/s00405-003-0679-7. Epub 2003 Sep 30. Eur Arch Otorhinolaryngol. 2004. PMID: 15138772
54 results