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Page 1
Retrospective analysis of persistent HyperCKemia with or without muscle weakness in a case series from Greece highlights vast DMD variant heterogeneity.
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
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
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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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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
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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
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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.
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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.
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