Selenti N - Search Results

1

Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast DMD variant heterogeneity.

Kekou K, Svingou M, Vogiatzakis N, Nitsa E, Veltra D, Marinakis NM, Tilemis FN, Tzetis M, Mitrakos A, Tsaroucha C, Selenti N, Papadimas GK, Papadopoulos C, Traeger-Synodinos J, Lochmuller H, Sofocleous C. Kekou K, et al. Among authors: selenti n. Expert Rev Mol Diagn. 2023 Jul-Dec;23(11):999-1010. doi: 10.1080/14737159.2023.2264181. Epub 2023 Oct 24. Expert Rev Mol Diagn. 2023. PMID: 37754746

2

Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype.

Kouvidi E, Zachaki S, Selenti N, Veltra D, Evmorfopoulou T, Tsoutsou E, Tzifa G, Sofocleous C, Gagos S, Mavrou A. Kouvidi E, et al. Among authors: selenti n. Gynecol Endocrinol. 2021 Apr;37(4):377-381. doi: 10.1080/09513590.2020.1865907. Epub 2020 Dec 28. Gynecol Endocrinol. 2021. PMID: 33356667 Free article.

3

Bone Marrow Failure in Fanconi Anemia: Clinical and Genetic Spectrum in a Cohort of 20 Pediatric Patients.

Kelaidi C, Makis A, Petrikkos L, Antoniadi K, Selenti N, Tzotzola V, Ioannidou ED, Tsitsikas K, Kitra V, Kalpini-Mavrou A, Fryssira H, Polychronopoulou S. Kelaidi C, et al. Among authors: selenti n. J Pediatr Hematol Oncol. 2019 Nov;41(8):612-617. doi: 10.1097/MPH.0000000000001549. J Pediatr Hematol Oncol. 2019. PMID: 31259830

4

Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly.

Tsoutsou E, Tzetis M, Giannikou K, Braoudaki M, Mitrakos A, Amenta S, Selenti N, Kanavakis E, Zafeiriou D, Kitsiou-Tzeli S, Fryssira H. Tsoutsou E, et al. Among authors: selenti n. Pediatr Res. 2017 Aug;82(2):253-260. doi: 10.1038/pr.2017.65. Epub 2017 May 24. Pediatr Res. 2017. PMID: 28422950

5

Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4.

Selenti N, Tzetis M, Braoudaki M, Giannikou K, Kitsiou-Tzeli S, Fryssira H. Selenti N, et al. Mol Cytogenet. 2015 Sep 30;8:73. doi: 10.1186/s13039-015-0174-z. eCollection 2015. Mol Cytogenet. 2015. PMID: 26430469 Free PMC article.

6

An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4.

Selenti N, Tzetis M, Braoudaki M, Gianikou K, Kitsiou-Tzeli S, Fryssira H. Selenti N, et al. Mol Cytogenet. 2015 Aug 12;8:64. doi: 10.1186/s13039-015-0169-9. eCollection 2015. Mol Cytogenet. 2015. PMID: 26269715 Free PMC article.

7

Investigation of FANCA mutations in Greek patients.

Selenti N, Sofocleous C, Kattamis A, Kolialexi A, Kitsiou S, Fryssira E, Polychronopoulou S, Kanavakis E, Mavrou A. Selenti N, et al. Anticancer Res. 2013 Aug;33(8):3369-74. Anticancer Res. 2013. PMID: 23898106

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