Traeger-Synodinos J - Search Results

1

Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management.

Traeger-Synodinos J, Vrettou C, Sofocleous C, Zurlo M, Finotti A, Gambari R; International Hemoglobinopathy Research Network (INHERENT). Traeger-Synodinos J, et al. Int J Mol Sci. 2024 Mar 17;25(6):3400. doi: 10.3390/ijms25063400. Int J Mol Sci. 2024. PMID: 38542374 Free PMC article. Review.

2

Multiplex sequence variation detection throughout the CFTR gene appropriate for preimplantation genetic diagnosis in populations with heterogeneity of cystic fibrosis mutations.

Vrettou C, Tzetis M, Traeger-Synodinos J, Palmer G, Kanavakis E. Vrettou C, et al. Mol Hum Reprod. 2002 Sep;8(9):880-6. doi: 10.1093/molehr/8.9.880. Mol Hum Reprod. 2002. PMID: 12200467

3

Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes.

Vrettou C, Traeger-Synodinos J, Tzetis M, Malamis G, Kanavakis E. Vrettou C, et al. Clin Chem. 2003 May;49(5):769-76. doi: 10.1373/49.5.769. Clin Chem. 2003. PMID: 12709368

4

An evaluation of PGD in clinical genetic services through 3 years application for prevention of beta-thalassaemia major and sickle cell thalassaemia.

Traeger-Synodinos J, Vrettou C, Palmer G, Tzetis M, Mastrominas M, Davies S, Kanavakis E. Traeger-Synodinos J, et al. Mol Hum Reprod. 2003 May;9(5):301-7. doi: 10.1093/molehr/gag038. Mol Hum Reprod. 2003. PMID: 12728023

5

Rare thalassemic syndrome caused by interaction of Hb Questembert (alpha1 codon 131, TCT>CCT, Ser>Pro) with an alpha-thalassemia-2 deletion: implications for diagnosis and management.

Stamoulakatou A, Athanasiou-Metaxa M, Traeger-Synodinos J, Lazaropoulou C, Harteveld K, Premetis E, Tsantali H, Zorai A, Giordano P, Papassotiriou I, Kanavakis E. Stamoulakatou A, et al. Blood Cells Mol Dis. 2004 Jan-Feb;32(1):118-23. doi: 10.1016/j.bcmd.2003.10.009. Blood Cells Mol Dis. 2004. PMID: 14757425

6

Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.

Vrettou C, Traeger-Synodinos J, Tzetis M, Palmer G, Sofocleous C, Kanavakis E. Vrettou C, et al. Hum Mutat. 2004 May;23(5):513-21. doi: 10.1002/humu.20022. Hum Mutat. 2004. PMID: 15108284

7

A rare 33 bp in-frame deletion (alpha63-74 or alpha64-74 or alpha65-75) in the alpha1-globin gene causing alpha(+)-thalassemia: a second observation.

Dimisianos G, Traeger-Synodinos J, Vrettou C, Papassotiriou I, Kanavakis E. Dimisianos G, et al. Hemoglobin. 2004 May;28(2):137-43. doi: 10.1081/hem-120035914. Hemoglobin. 2004. PMID: 15182056

8

Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.

Traeger-Synodinos J, Vrettou C, Kanavakis E. Traeger-Synodinos J, et al. Methods Mol Biol. 2008;444:133-45. doi: 10.1007/978-1-59745-066-9_10. Methods Mol Biol. 2008. PMID: 18425477

9

Cell-free DNA levels in acute myocardial infarction patients during hospitalization.

Destouni A, Vrettou C, Antonatos D, Chouliaras G, Traeger-Synodinos J, Patsilinakos S, Kitsiou-Tzeli S, Tsigas D, Kanavakis E. Destouni A, et al. Acta Cardiol. 2009 Feb;64(1):51-7. doi: 10.2143/AC.64.1.2034362. Acta Cardiol. 2009. PMID: 19317298

10

An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.

Lederer CW, Basak AN, Aydinok Y, Christou S, El-Beshlawy A, Eleftheriou A, Fattoum S, Felice AE, Fibach E, Galanello R, Gambari R, Gavrila L, Giordano PC, Grosveld F, Hassapopoulou H, Hladka E, Kanavakis E, Locatelli F, Old J, Patrinos GP, Romeo G, Taher A, Traeger-Synodinos J, Vassiliou P, Villegas A, Voskaridou E, Wajcman H, Zafeiropoulos A, Kleanthous M. Lederer CW, et al. Hemoglobin. 2009;33(3):163-76. doi: 10.1080/03630260903089177. Hemoglobin. 2009. PMID: 19657830

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