Efterpi Pavlidou
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Explore the profile of Efterpi Pavlidou including associated specialties, affiliations and a list of published articles.
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31
Citations
154
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Recent Articles
1.
Papadopoulou S, Anagnostopouplou A, Katsarou D, Megari K, Efthymiou E, Argyriadis A, et al.
Healthcare (Basel)
. 2025 Jan;
13(1.
PMID: 39791659
This study presents a comprehensive investigation into the correlation between Rare Diseases and Syndromes (RDS) and the dysphagic disorders manifested during childhood and adulthood in affected patients. Dysphagia is characterized...
2.
Papadopoulou S, Anagnostopoulou A, Katsarou D, Megari K, Efthymiou E, Argyriadis A, et al.
Children (Basel)
. 2025 Jan;
11(12.
PMID: 39767955
A specific deletion on the short arm of chromosome 5 (5p) is the hallmark of the rare genetic syndrome called Cri du Chat Syndrome (CdCS). It causes severe difficulty with...
3.
Keramida C, Papoulidis I, Pappa E, Liehr T, Kalmantis K, Gerede A, et al.
Exp Ther Med
. 2024 Apr;
27(6):241.
PMID: 38660521
Numerous rearrangements in the 8p23 chromosomal region have been reported; included in these rearrangements are isolated deletions in this area. Such deletions are associated with a wide range of phenotypic...
4.
Sotiriou S, Samara A, Anastasakis E, Zikopoulos A, Papoulidis I, Manolakos E, et al.
Cureus
. 2024 Apr;
16(2):e55142.
PMID: 38558627
We present the case of a 35-year-old pregnant woman who visited our department for a routine ultrasonography screening scan for fetus anatomy during the 22nd week of gestation. Our report...
5.
Kury S, Stanton J, van Woerden G, Hsieh T, Rosenfelt C, Scott-Boyer M, et al.
medRxiv
. 2024 Jan;
PMID: 38293138
Neurodevelopmental proteasomopathies represent a distinctive category of neurodevelopmental disorders (NDD) characterized by genetic variations within the 26S proteasome, a protein complex governing eukaryotic cellular protein homeostasis. In our comprehensive study,...
6.
Tzelepis K, Zacharouli K, Samara A, Koutras A, Kontomanolis E, Perivoliotis K, et al.
Surg J (N Y)
. 2023 May;
9(2):e71-e74.
PMID: 37192958
In this report we present a rare case of a large cyst of Skene gland in a female patient with a palpable vaginal mass persisting for at least 2 years. ...
7.
Papadopoulou S, Pavlidou E, Argyris G, Flouda T, Koukoutsidi P, Krikonis K, et al.
J Pers Med
. 2022 Apr;
12(4).
PMID: 35455763
Although the impact of epilepsy on expressive language is heavily discussed, researched, and scientifically grounded, a limited volume of research points in the opposite direction. What about the causal relationship...
8.
Frasca A, Pavlidou E, Bizzotto M, Gao Y, Balestra D, Pinotti M, et al.
Neurol Genet
. 2022 Mar;
8(2):e666.
PMID: 35280940
Background And Objectives: CDKL5 deficiency disorder (CDD) is a neurodevelopmental encephalopathy characterized by early-onset epilepsy and impaired psychomotor development. Variations in the X-linked gene coding for a kinase cause CDD....
9.
Zimmels S, Balfour-Lynn I, Christodoulou L, Pantazi M, Pavlidou E, Pitt M, et al.
Dev Med Child Neurol
. 2021 Oct;
64(4):518-522.
PMID: 34601721
Oropharyngeal dysphagia can cause chronic aspiration leading to significant respiratory symptoms. When dysphagia is diagnosed, an underlying cause is sought. We present a case series of 15 children diagnosed aged...
10.
Vrachnis N, Papoulidis I, Vrachnis D, Siomou E, Antonakopoulos N, Oikonomou S, et al.
Mol Cytogenet
. 2021 Jul;
14(1):39.
PMID: 34303382
Background: The interstitial 6p22.3 deletions concern rare chromosomal events affecting numerous aspects of both physical and mental development. The syndrome is characterized by partial deletion of chromosome 6, which may...