Thomaidis L - Search Results

1

Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report.

Orru S, Papoulidis I, Siomou E, Papadimitriou DT, Sotiriou S, Nikolaidis P, Eleftheriades M, Papanikolaou E, Thomaidis L, Manolakos E. Orru S, et al. Among authors: thomaidis l. Biomed Rep. 2019 Jun;1(1):1-5. doi: 10.3892/br.2019.1210. Epub 2019 May 13. Biomed Rep. 2019. PMID: 31258897 Free PMC article.

2

A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2.

Siomou E, Manolakos E, Petersen M, Thomaidis L, Gyftodimou Y, Orru S, Papoulidis I. Siomou E, et al. Among authors: thomaidis l. Eur J Med Genet. 2012 Nov;55(11):641-5. doi: 10.1016/j.ejmg.2012.07.002. Epub 2012 Jul 25. Eur J Med Genet. 2012. PMID: 22842075

3

Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report.

Papoulidis I, Oikonomidou E, Orru S, Siomou E, Kontodiou M, Eleftheriades M, Bacoulas V, Cigudosa JC, Suela J, Thomaidis L, Manolakos E. Papoulidis I, et al. Among authors: thomaidis l. Mol Med Rep. 2014 Jan;9(1):163-5. doi: 10.3892/mmr.2013.1788. Epub 2013 Nov 11. Mol Med Rep. 2014. PMID: 24220582

4

Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature.

Manolakos E, Vetro A, Garas A, Thomaidis L, Kefalas K, Kitsos G, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: thomaidis l. Exp Ther Med. 2014 Apr;7(4):953-957. doi: 10.3892/etm.2014.1520. Epub 2014 Feb 6. Exp Ther Med. 2014. PMID: 24669257 Free PMC article.

5

Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay.

Papoulidis I, Paspaliaris V, Papageorgiou E, Siomou E, Dagklis T, Sotiriou S, Thomaidis L, Manolakos E. Papoulidis I, et al. Among authors: thomaidis l. Cytogenet Genome Res. 2015;145(1):19-24. doi: 10.1159/000381568. Epub 2015 Apr 24. Cytogenet Genome Res. 2015. PMID: 25925190

6

Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.

Papoulidis I, Paspaliaris V, Siomou E, Orru S, Murru R, Sifakis S, Nikolaidis P, Garas A, Sotiriou S, Thomaidis L, Manolakos E. Papoulidis I, et al. Among authors: thomaidis l. Mol Cytogenet. 2015 Sep 17;8:71. doi: 10.1186/s13039-015-0175-y. eCollection 2015. Mol Cytogenet. 2015. PMID: 26388939 Free PMC article.

7

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).

Manolakos E, Orru S, Neroutsou R, Kefalas K, Louizou E, Papoulidis I, Thomaidis L, Peitsidis P, Sotiriou S, Kitsos G, Tsoplou P, Petersen MB, Metaxotou A. Manolakos E, et al. Among authors: thomaidis l. Mol Cytogenet. 2009 Dec 9;2:26. doi: 10.1186/1755-8166-2-26. Mol Cytogenet. 2009. PMID: 20003197 Free PMC article.

8

Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature.

Manolakos E, Sifakis S, Sotiriou S, Peitsidis P, Eleftheriades M, Mersinias V, Liehr T, Thomaidis L, Kitsos G, Papoulidis I, Petersen MB, Orru S. Manolakos E, et al. Among authors: thomaidis l. Clin Dysmorphol. 2012 Apr;21(2):101-105. doi: 10.1097/MCD.0b013e32834e9279. Clin Dysmorphol. 2012. PMID: 22391621 Review. No abstract available.

9

A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics.

Lagou M, Papoulidis I, Orru S, Papadopoulos V, Daskalakis G, Kontodiou M, Anastasakis E, Petersen MB, Kitsos G, Thomaidis L, Manolakos E. Lagou M, et al. Among authors: thomaidis l. Mol Cytogenet. 2014 Dec 3;7(1):92. doi: 10.1186/s13039-014-0092-5. eCollection 2014. Mol Cytogenet. 2014. PMID: 25506395 Free PMC article.

10

Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.

Kontodiou M, Daskalakis G, Vetro A, Paspaliaris V, Papaioannou G, Dagklis T, Tsakiridis I, Ziegler M, Liehr T, Thomaidis L, Papoulidis I, Manolakos E. Kontodiou M, et al. Among authors: thomaidis l. Cytogenet Genome Res. 2015;147(2-3):118-23. doi: 10.1159/000442583. Epub 2015 Dec 18. Cytogenet Genome Res. 2015. PMID: 26681178

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