Traeger-Synodinos J - Search Results

1

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. 2019;1885:207-219. doi: 10.1007/978-1-4939-8889-1_14. Methods Mol Biol. 2019. PMID: 30506200

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

Unusual phenotypic observations associated with a rare HbH disease genotype (- -Med/alphaTSaudialpha): implications for clinical management.

Traeger-Synodinos J, Papassotiriou I, Karagiorga M, Premetis E, Kanavakis E, Stamoulakatou A. Traeger-Synodinos J, et al. Br J Haematol. 2002 Oct;119(1):265-7. doi: 10.1046/j.1365-2141.2002.03777.x. Br J Haematol. 2002. PMID: 12358934 Free article.

4

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

5

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

6

Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels.

Skarmoutsou C, Papassotiriou I, Traeger-Synodinos J, Stamou H, Ladis V, Metaxotou-Mavrommati A, Stamoulakatou A, Kanavakis E. Skarmoutsou C, et al. Haematologica. 2003 Jun;88(6):631-6. Haematologica. 2003. PMID: 12801838

7

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

8

A rare example that coinheritance of a severe form of beta-thalassemia and alpha-thalassemia interact in a "synergistic" manner to balance the phenotype of classic thalassemic syndromes.

Kanavakis E, Traeger-Synodinos J, Lafioniatis S, Lazaropoulou C, Liakopoulou T, Paleologos G, Metaxotou-Mavrommati A, Stamoulakatou A, Papassotiriou I. Kanavakis E, et al. Blood Cells Mol Dis. 2004 Mar-Apr;32(2):319-24. doi: 10.1016/j.bcmd.2003.12.005. Blood Cells Mol Dis. 2004. PMID: 15003825

9

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

10

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

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