Kanavakis E - Search Results

1

A minimal set of SNPs for the noninvasive prenatal diagnosis of β-thalassaemia.

Papasavva TE, Lederer CW, Traeger-Synodinos J, Mavrou A, Kanavakis E, Ioannou C, Makariou C, Kleanthous M. Papasavva TE, et al. Among authors: kanavakis e. Ann Hum Genet. 2013 Mar;77(2):115-24. doi: 10.1111/ahg.12004. Epub 2013 Jan 31. Ann Hum Genet. 2013. PMID: 23362932

2

ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia.

Shammas C, Papasavva T, Felekis X, Christophorou C, Roomere H, Synodinos JT, Kanavakis E, El-Khateeb M, Hamamy H, Mahmoud T, Shboul M, El Beshlawy A, Filon D, Hussein IR, Galanello R, Romeo G, Kleanthous M. Shammas C, et al. Among authors: kanavakis e. Clin Chem Lab Med. 2010 Dec;48(12):1713-8. doi: 10.1515/CCLM.2010.331. Epub 2010 Aug 13. Clin Chem Lab Med. 2010. PMID: 20704537

3

Microsatellite markers within the α-globin gene cluster for robust preimplantation genetic diagnosis of severe α-thalassemia syndromes in Mediterranean populations.

Destouni A, Christopoulos G, Vrettou C, Kakourou G, Kleanthous M, Traeger-Synodinos J, Kanavakis E. Destouni A, et al. Among authors: kanavakis e. Hemoglobin. 2012;36(3):253-64. doi: 10.3109/03630269.2012.666512. Epub 2012 Mar 27. Hemoglobin. 2012. PMID: 22452522

4

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. Among authors: kanavakis e. Hemoglobin. 2009;33(3):163-76. doi: 10.1080/03630260903089177. Hemoglobin. 2009. PMID: 19657830

5

Genotyping of β-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.

Durmaz B, Ozkinay F, Onay H, Karaca E, Aydinok Y, Tavmergen E, Vrettou C, Traeger-Synodinos J, Kanavakis E. Durmaz B, et al. Among authors: kanavakis e. Hemoglobin. 2012;36(3):230-43. doi: 10.3109/03630269.2012.675891. Epub 2012 Apr 23. Hemoglobin. 2012. PMID: 22524255

6

Multi-allele DNA biosensor for the rapid genotyping of 'nondeletion' alpha thalassaemia mutations in HBA1 and HBA2 genes by means of multiplex primer extension reaction.

Petropoulou M, Poula A, Traeger-Synodinos J, Kanavakis E, Christopoulos TK, Ioannou PC. Petropoulou M, et al. Among authors: kanavakis e. Clin Chim Acta. 2015 Jun 15;446:241-7. doi: 10.1016/j.cca.2015.04.016. Epub 2015 Apr 17. Clin Chim Acta. 2015. PMID: 25892676

7

Two new beta-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention.

Phylipsen M, Amato A, Cappabianca MP, Traeger-Synodinos J, Kanavakis E, Basak N, Galanello R, Tuveri T, Ivaldi G, Harteveld CL, Giordano PC. Phylipsen M, et al. Among authors: kanavakis e. Haematologica. 2009 Sep;94(9):1289-92. doi: 10.3324/haematol.2009.007989. Haematologica. 2009. PMID: 19734421 Free PMC article.

8

A generic, flexible protocol for preimplantation human leukocyte antigen typing alone or in combination with a monogenic disease, for rapid case work-up and application.

Kakourou G, Destouni A, Vrettou C, Traeger-Synodinos J, Kanavakis E. Kakourou G, et al. Among authors: kanavakis e. Hemoglobin. 2014;38(1):49-55. doi: 10.3109/03630269.2013.842582. Epub 2013 Oct 16. Hemoglobin. 2014. PMID: 24131134

9

A simplified approach for FSHD molecular testing.

Papanikos F, Skoulatou C, Sakellariou P, Kekou K, Christopoulos TK, Kanavakis E, Traeger-Synodinos J, Ioannou PC. Papanikos F, et al. Among authors: kanavakis e. Clin Chim Acta. 2014 Feb 15;429:96-103. doi: 10.1016/j.cca.2013.11.032. Epub 2013 Dec 7. Clin Chim Acta. 2014. PMID: 24321734

10

A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.

Phylipsen M, Traeger-Synodinos J, van der Kraan M, van Delft P, Bakker G, Geerts M, Kanavakis E, Stamoulakatou A, Karagiorga M, Giordano PC, Harteveld CL. Phylipsen M, et al. Among authors: kanavakis e. Eur J Haematol. 2012 Apr;88(4):356-62. doi: 10.1111/j.1600-0609.2012.01748.x. Epub 2012 Feb 11. Eur J Haematol. 2012. PMID: 22324317

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