Antoniadi T - Search Results

1

High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness.

Antoniadi T, Rabionet R, Kroupis C, Aperis GA, Economides J, Petmezakis J, Economou-Petersen E, Estivill X, Petersen MB. Antoniadi T, et al. Clin Genet. 1999 May;55(5):381-2. Clin Genet. 1999. PMID: 10422812 No abstract available.

2

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. 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

3

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors.

Antoniadi T, Hatzis T, Kroupis C, Economou-Petersen E, Petersen MB. Antoniadi T, et al. Am J Hematol. 1999 Aug;61(4):265-7. doi: 10.1002/(sici)1096-8652(199908)61:4<265::aid-ajh8>3.0.co;2-#. Am J Hematol. 1999. PMID: 10440914 Free article.

4

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. 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

5

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: antoniadi t. 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

6

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

7

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

8

A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis.

Antoniadi T, Yapijakis C, Kaminopetros P, Makatsoris C, Velissariou V, Vassilopoulos D, Petersen MB. Antoniadi T, et al. Prenat Diagn. 2002 May;22(5):425-9. doi: 10.1002/pd.325. Prenat Diagn. 2002. PMID: 12001201

9

Increased resistance to activated protein C and factor V Leiden in recurrent abortions. Review of other hypercoagulability factors.

Hatzis T, Cardamakis E, Drivalas E, Makatsoris K, Bevan D, Pantos C, Malliopoulou V, Tsagaris N, Kreatsa O, Antoniadi T, Petersen MB, Karageorgiou H, Mantouvalos H. Hatzis T, et al. Among authors: antoniadi t. Eur J Contracept Reprod Health Care. 1999 Sep;4(3):135-44. Eur J Contracept Reprod Health Care. 1999. PMID: 10574639 Clinical Trial.

10

Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.

Velissariou V, Antoniadi T, Patsalis P, Christopoulou S, Hatzipouliou A, Donoghue J, Bakou K, Kaminopetros P, Athanassiou V, Petersen MB. Velissariou V, et al. Among authors: antoniadi t. Prenat Diagn. 2001 Jun;21(6):484-7. doi: 10.1002/pd.79. Prenat Diagn. 2001. PMID: 11438955

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