Touliatou V - Search Results

1

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: touliatou v. 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

2

Rhabdomyosarcoma in a patient with Noonan syndrome phenotype and review of the literature.

Moschovi M, Touliatou V, Papadopoulou A, Mayakou MA, Nikolaidou-Karpathiou P, Kitsiou-Tzeli S. Moschovi M, et al. Among authors: touliatou v. J Pediatr Hematol Oncol. 2007 May;29(5):341-4. doi: 10.1097/MPH.0b013e31805d8f57. J Pediatr Hematol Oncol. 2007. PMID: 17483716

3

Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.

Kitsiou-Tzeli S, Sismani C, Ioannides M, Bashiardes S, Ketoni A, Touliatou V, Kolialexi A, Mavrou A, Kanavakis E, Patsalis PC. Kitsiou-Tzeli S, et al. Among authors: touliatou v. Eur J Med Genet. 2007 Jan-Feb;50(1):73-8. doi: 10.1016/j.ejmg.2006.09.004. Epub 2006 Oct 11. Eur J Med Genet. 2007. PMID: 17194633

4

Infective endocarditis in an adult patient with CHARGE association: a case report.

Antonatos D, Patsilinakos S, Touliatou V, Sotirelos K, Frisira E, Tsigas D. Antonatos D, et al. Among authors: touliatou v. Angiology. 2006 Oct-Nov;57(5):631-5. doi: 10.1177/0003319706293148. Angiology. 2006. PMID: 17067987

5

Saethre-Chotzen syndrome with severe developmental delay associated with deletion of chromosomic region 7p15 --> pter.

Touliatou V, Mavrou A, Kolialexi A, Kanavakis E, Kitsiou-Tzeli S. Touliatou V, et al. Genet Couns. 2007;18(3):295-301. Genet Couns. 2007. PMID: 18019370

6

Distal del(4) (q33) syndrome: detailed clinical presentation and molecular description with array-CGH.

Kitsiou-Tzeli S, Sismani C, Koumbaris G, Ioannides M, Kanavakis E, Kolialexi A, Mavrou A, Touliatou V, Patsalis PC. Kitsiou-Tzeli S, et al. Among authors: touliatou v. Eur J Med Genet. 2008 Jan-Feb;51(1):61-7. doi: 10.1016/j.ejmg.2007.09.004. Epub 2007 Oct 2. Eur J Med Genet. 2008. PMID: 17998173

7

Clinical manifestations in 17 Greek patients with Goldenhar syndrome.

Touliatou V, Fryssira H, Mavrou A, Kanavakis E, Kitsiou-Tzeli S. Touliatou V, et al. Genet Couns. 2006;17(3):359-70. Genet Couns. 2006. PMID: 17100205

8

Conventional cytogenetics and fluorescence in situ hybridization in persistent cytopenias and myelodysplastic syndromes in childhood.

Touliatou V, Kolialexi A, Tsangaris GT, Moschovi M, Polychronopoulou S, Mavrou A. Touliatou V, et al. Anticancer Res. 2004 Nov-Dec;24(6):3945-9. Anticancer Res. 2004. PMID: 15736436 Free article.

9

Use of annexin V antibody to identify apoptotic cells during pregnancy.

Kolialexi A, Tsangaris GT, Mavrou A, Antsaklis A, Tzortzatou F, Touliatou V, Metaxotou C. Kolialexi A, et al. Among authors: touliatou v. Ann N Y Acad Sci. 2001 Sep;945:145-50. doi: 10.1111/j.1749-6632.2001.tb03876.x. Ann N Y Acad Sci. 2001. PMID: 11708469

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