Petersen MB - Search Results

1

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: petersen mb. ORL J Otorhinolaryngol Relat Spec. 2002 Sep-Oct;64(5):321-3. doi: 10.1159/000066088. ORL J Otorhinolaryngol Relat Spec. 2002. PMID: 12417772

2

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: petersen mb. 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

3

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: petersen mb. 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

4

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: petersen mb. 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

5

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: petersen mb. 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

6

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: petersen mb. Genet Test Mol Biomarkers. 2010 Apr;14(2):189-92. doi: 10.1089/gtmb.2009.0136. Genet Test Mol Biomarkers. 2010. PMID: 20059378

7

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. 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

8

Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness.

Antoniadi T, Grønskov K, Sand A, Pampanos A, Brøndum-Nielsen K, Petersen MB. Antoniadi T, et al. Among authors: petersen mb. Hum Mutat. 2000;16(1):7-12. doi: 10.1002/1098-1004(200007)16:1<7::AID-HUMU2>3.0.CO;2-A. Hum Mutat. 2000. PMID: 10874298

9

Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation.

Antoniadi T, Pampanos A, Petersen MB. Antoniadi T, et al. Among authors: petersen mb. Prenat Diagn. 2001 Jan;21(1):10-3. doi: 10.1002/1097-0223(200101)21:1<10::aid-pd968>3.0.co;2-h. Prenat Diagn. 2001. PMID: 11180233

10

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: petersen mb. 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

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