Despina Apostolopoulou
Overview
Explore the profile of Despina Apostolopoulou including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
5
Citations
21
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Sarafidou T, Galliopoulou E, Apostolopoulou D, Fragkiadakis G, Moschonas N
Genes (Basel)
. 2023 Mar;
14(3).
PMID: 36980839
, the causative gene for the manifestation of the fragile site, encodes a well-conserved nuclear protein characterized as a non-core spliceosomal component. Pre-mRNA splicing perturbations have been linked with neurodevelopmental...
2.
Apostolopoulou D, Kaxira O, Hatzaki A, Panagopoulos K, Alexandrou K, Stratoudakis A, et al.
Cleft Palate Craniofac J
. 2018 Mar;
55(8):1092-1102.
PMID: 29561715
Introduction: Craniosynostosis, the premature fusion of cranial sutures, is usually divided into 2 major categories: syndromic and nonsyndromic. Mutations in the , , , , and genes cause the common...
3.
Psinakis F, Katseli A, Koutsandrea C, Frangia K, Florentin L, Apostolopoulou D, et al.
Anticancer Res
. 2017 Oct;
37(10):5719-5726.
PMID: 28982892
Background/aim: Uveal melanoma is the most common primary adult intraocular malignancy. It is known to have a strong metastatic potential, fatal for the vast majority of patients. In recent years,...
4.
Hatzaki A, Sifakis S, Apostolopoulou D, Bouzarelou D, Konstantinidou A, Kappou D, et al.
Am J Med Genet A
. 2011 Sep;
155A(10):2426-35.
PMID: 21910223
Fibroblast Growth Factor Receptor 3 (FGFR3) related skeletal dysplasias are caused by mutations in the FGFR3 gene that result in increased activation of the receptors causing alterations in the process...
5.
Apostolopoulou D, Stratoudakis A, Hatzaki A, Kaxira O, Panagopoulos K, Kollia P, et al.
Cleft Palate Craniofac J
. 2011 Mar;
49(1):109-13.
PMID: 21385071
Craniofrontonasal syndrome is mainly characterized by frontonasal dysplasia, telorbitism, a broad nasal root, and frequently a bifid nose and coronal craniosynostosis. Craniofrontonasal syndrome is an X-linked disorder with an unusual...