Antoniadi T - Search Results

1

Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations.

Tzetis M, Kanavakis E, Antoniadi T, Doudounakis S, Adam G, Kattamis C. Tzetis M, et al. Among authors: antoniadi t. Hum Genet. 1997 Jan;99(1):121-5. doi: 10.1007/s004390050324. Hum Genet. 1997. PMID: 9003508

2

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.

Velissariou V, Antoniadi T, Gyftodimou J, Bakou K, Grigoriadou M, Christopoulou S, Hatzipouliou A, Donoghue J, Karatzis P, Katsarou E, Petersen MB. Velissariou V, et al. Among authors: antoniadi t. Eur J Hum Genet. 2002 Nov;10(11):694-8. doi: 10.1038/sj.ejhg.5200867. Eur J Hum Genet. 2002. PMID: 12404100

3

Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis.

Radivojevic D, Djurisic M, Lalic T, Guc-Scekic M, Savic J, Minic P, Antoniadi T, Tzetis M, Kanavakis E. Radivojevic D, et al. Among authors: antoniadi t. Genet Test. 2004 Fall;8(3):276-80. doi: 10.1089/gte.2004.8.276. Genet Test. 2004. PMID: 15727251

4

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

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: 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

6

A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis.

Vrettou C, Palmer G, Kanavakis E, Tzetis M, Antoniadi T, Mastrominas M, Traeger-Synodinos J. Vrettou C, et al. Among authors: antoniadi t. Prenat Diagn. 1999 Dec;19(13):1209-16. Prenat Diagn. 1999. PMID: 10660957

7

Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.

Kanavakis E, Tzetis M, Antoniadi T, Pistofidis G, Milligos S, Kattamis C. Kanavakis E, et al. Among authors: antoniadi t. Mol Hum Reprod. 1998 Apr;4(4):333-7. doi: 10.1093/molehr/4.4.333. Mol Hum Reprod. 1998. PMID: 9620832

8

Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation.

Kanavakis E, Tzetis M, Antoniadi T, Traeger-Synodinos J, Doudounakis S, Adam G, Matsaniotis N, Kattamis C. Kanavakis E, et al. Among authors: antoniadi t. Hum Genet. 1995 Sep;96(3):364-6. doi: 10.1007/BF00210426. Hum Genet. 1995. PMID: 7544320

9

Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients.

Tzetis M, Kanavakis E, Antoniadi T, Traeger-Synodinos J, Doudounakis S, Adam G, Kattamis C. Tzetis M, et al. Among authors: antoniadi t. Mol Cell Probes. 1995 Aug;9(4):283-5. doi: 10.1016/s0890-8508(95)90169-8. Mol Cell Probes. 1995. PMID: 7477025

10

Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation.

Kanavakis E, Tzetis M, Antoniadi T, Trager-Synodinos J, Kattamis C, Doudounakis S, Adam G. Kanavakis E, et al. Among authors: antoniadi t. J Med Genet. 1995 May;32(5):406-7. doi: 10.1136/jmg.32.5.406. J Med Genet. 1995. PMID: 7542347 Free PMC article. No abstract available.

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