Leze E - Search Results

1

An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.

Tzetis M, Stefanaki K, Syrmou A, Kosma K, Leze E, Giannikou K, Oikonomakis V, Sofocleous C, Choulakis M, Kolialexi A, Makrythanasis P, Kitsiou-Tzeli S. Tzetis M, et al. Among authors: leze e. Birth Defects Res A Clin Mol Teratol. 2012 Jul;94(7):561-6. doi: 10.1002/bdra.23038. Epub 2012 Jun 22. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22730277

2

Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.

Kitsiou-Tzeli S, Frysira H, Giannikou K, Syrmou A, Kosma K, Kakourou G, Leze E, Sofocleous C, Kanavakis E, Tzetis M. Kitsiou-Tzeli S, et al. Among authors: leze e. Gene. 2012 Jan 15;492(1):319-24. doi: 10.1016/j.gene.2011.10.023. Epub 2011 Oct 20. Gene. 2012. PMID: 22037486

3

Milroy's primary congenital lymphedema in a male infant and review of the literature.

Kitsiou-Tzeli S, Vrettou C, Leze E, Makrythanasis P, Kanavakis E, Willems P. Kitsiou-Tzeli S, et al. Among authors: leze e. In Vivo. 2010 May-Jun;24(3):309-14. In Vivo. 2010. PMID: 20555004 Review.

4

Long term follow up of a woman with classic form of Ehlers-Danlos syndrome associated with rare manifestations and review of the literature.

Kitsiou-Tzeli S, Leze E, Salavoura K, Giannatou E, Fretzayas A, Makrithanasis P, Kanavakis E. Kitsiou-Tzeli S, et al. Among authors: leze e. Genet Couns. 2010;21(1):75-83. Genet Couns. 2010. PMID: 20420033

5

Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation.

Thomaidis L, Kitsiou-Tzeli S, Critselis E, Drandakis H, Touliatou V, Mantoudis S, Leze E, Destouni A, Traeger-Synodinos J, Kafetzis D, Kanavakis E. Thomaidis L, et al. Among authors: leze e. World J Pediatr. 2012 Nov;8(4):309-16. doi: 10.1007/s12519-012-0374-0. Epub 2012 Nov 15. World J Pediatr. 2012. PMID: 23151857

6

Author reply: To PMID 23151857.

Leze E, Thomaidis L, Kitsiou-Tzeli S, Kanavakis E. Leze E, et al. World J Pediatr. 2013 Feb;9(1):90-1. doi: 10.1007/s12519-013-0409-1. World J Pediatr. 2013. PMID: 23389336 No abstract available.

7

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.

Manolakos E, Sarri C, Vetro A, Kefalas K, Leze E, Sofocleus C, Kitsos G, Merou K, Kokotas H, Papadopoulou A, Attilakos A, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Among authors: leze e. Mol Cytogenet. 2011 Feb 23;4(1):6. doi: 10.1186/1755-8166-4-6. Mol Cytogenet. 2011. PMID: 21345209 Free PMC article.

8

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.

Manolakos E, Sarri C, Vetro A, Kefalas K, Leze E, Sofocleus C, Kitsos G, Merou K, Kokotas H, Papadopoulou A, Attilakos A, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Among authors: leze e. Mol Cytogenet. 2011 Apr 16;4(1):11. doi: 10.1186/1755-8166-4-11. Mol Cytogenet. 2011. PMID: 21496283 Free PMC article. No abstract available.

9

Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene.

Kitsiou-Tzeli S, Willems P, Kosmadaki M, Leze E, Vrettou C, Kanavakis E, Katsarou A. Kitsiou-Tzeli S, et al. Among authors: leze e. J Dermatol. 2011 Dec;38(12):1205-8. doi: 10.1111/j.1346-8138.2011.01265.x. Epub 2011 Sep 23. J Dermatol. 2011. PMID: 21950490 No abstract available.

10

Advantages of evaluating mean nuclear volume as an adjunct parameter in prostate cancer.

Leze E, Maciel-Osorio CF, Mandarim-de-Lacerda CA. Leze E, et al. PLoS One. 2014 Jul 9;9(7):e102156. doi: 10.1371/journal.pone.0102156. eCollection 2014. PLoS One. 2014. PMID: 25007252 Free PMC article.

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