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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 2
2010 2
2011 2
2012 4
2013 2
2014 6
2015 4
2016 1
2017 2
2018 1
2019 5
2020 4
2021 6
2022 3
2023 2
2024 4

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46 results

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Page 1
The multiple faces of Danon disease.
Ntelios D, Parcharidou D, Zegkos T, Paraskevaidis S, Manolakos E, Papoulidis I, Vassilikos V, Karvounis H, Efthimiadis G. Ntelios D, et al. Among authors: papoulidis i. Hellenic J Cardiol. 2021 Mar-Apr;62(2):178-179. doi: 10.1016/j.hjc.2020.06.004. Epub 2020 Jun 15. Hellenic J Cardiol. 2021. PMID: 32553999 Free article. No abstract available.
Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization.
Papadopoulou Z, Papoulidis I, Sifakis S, Markopoulos G, Vetro A, Vlaikou AM, Ziegler M, Liehr T, Thomaidis L, Zuffardi O, Syrrou M, George K, Manolakos E. Papadopoulou Z, et al. Among authors: papoulidis i. Mol Med Rep. 2017 Dec;16(6):8808-8818. doi: 10.3892/mmr.2017.7760. Epub 2017 Oct 10. Mol Med Rep. 2017. PMID: 29039589 Free PMC article. Review.
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: papoulidis i. Clin Dysmorphol. 2012 Apr;21(2):101-105. doi: 10.1097/MCD.0b013e32834e9279. Clin Dysmorphol. 2012. PMID: 22391621 Review. No abstract available.
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I. Sifakis S, et al. Among authors: papoulidis i. Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):284-93. doi: 10.1002/bdra.23213. Epub 2014 Feb 12. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24677675 Review.
A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype.
Efthimiadis G, Zegkos T, Meditskou S, Karamitsos T, Manolakos E, Papoulidis I, Orru S, Cadeddu Dessalvi C, Karvounis H, Parcharidou D. Efthimiadis G, et al. Among authors: papoulidis i. Hellenic J Cardiol. 2021 Jan-Feb;62(1):95-98. doi: 10.1016/j.hjc.2020.04.014. Epub 2020 May 7. Hellenic J Cardiol. 2021. PMID: 32387596 Free article. No abstract available.
46 results