Kyriaki Papadopoulou-Legbelou
Overview
Explore the profile of Kyriaki Papadopoulou-Legbelou including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
100
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Recent Articles
1.
Gkiourtzis N, Panagopoulou P, Papadopoulou-Legbelou K, Chantavaridou S, Tramma D
Clin Nephrol Case Stud
. 2024 Apr;
12:32-35.
PMID: 38596164
A 12-year-old boy was transferred to our pediatric department from a rural hospital for fever, cough, and vomiting associated with thrombocytopenia, non-immune hemolytic anemia, and acute kidney injury, leading to...
2.
Moutafi M, Ververi A, Papadopoulou-Legbelou K, Gkiourtzis N, Fotoulaki M, Mataftsi A
Clin Dysmorphol
. 2024 Feb;
33(2):95-98.
PMID: 38411000
No abstract available.
3.
Papadopoulou-Legbelou K, Ntoumpara M, Kavga M, Kotanidou E, Papoulidis I, Galli-Tsinopoulou A, et al.
Case Rep Genet
. 2024 Jan;
2024:8860889.
PMID: 38283849
Dilated cardiomyopathy with ataxia syndrome is a rare mitochondrial disease caused by autosomal recessive mutations in the gene. The disease has been described in detail in the Canadian Hutterite population,...
4.
Lampidi S, Maritsi D, Charakida M, Eleftheriou I, Farmaki E, Spyridis N, et al.
Eur J Pediatr
. 2024 Jan;
183(4):1693-1702.
PMID: 38214810
Conclusion: MIS-C is a novel, infrequent but serious disease entity. Cardiac manifestations included myocarditis and pericarditis, which resolved in most patients before discharge. Timely initiation of immunomodulatory therapy was shown...
5.
Moutafi M, Gkiourtzis N, Ververi A, Kavga M, Morichovitou A, Papadopoulou-Legbelou K, et al.
Am J Med Genet A
. 2023 Aug;
194(1):88-93.
PMID: 37632712
We describe a 2-month-old female infant with macroglossia, macrosomia, omphalocele, neonatal hypoglycemia, earlobe creases, low nasal bridge, midface retrusion, syndromic facies and multiple cutaneous and hepatic hemangiomas (HH). Genetic evaluation...
6.
Gkiourtzis N, Tramma D, Papadopoulou-Legbelou K, Moutafi M, Evangeliou A
Am J Med Genet A
. 2023 Aug;
191(12):2843-2849.
PMID: 37565517
Mitochondrial myopathy is a severe metabolic myopathy related to nuclear or mitochondrial DNA dysfunction. We present a rare case of mitochondrial myopathy, presented with multiple episodes of proximal muscle weakness,...
7.
Eleftheriou I, Maritsi D, Lampidi S, Charisi K, Vantsi P, Skourti K, et al.
Pediatr Infect Dis J
. 2023 Jan;
42(2):122-124.
PMID: 36638397
In this nationwide retrospective study, a substantial decline in the incidence of multisystem inflammatory syndrome in children over 3 successive pandemic waves characterized by different severe acute respiratory syndrome coronavirus...
8.
Stasinou E, Emmanouilidou-Fotoulaki E, Kavga M, Sotiriadou F, Lambropoulos A, Fotoulaki M, et al.
Nutrients
. 2022 Sep;
14(17).
PMID: 36079710
Non-alcoholic fatty liver disease (NAFLD) shares several risk factors with atherosclerosis, as it is associated with components of the metabolic syndrome. However, genetic variations have also been linked to the...
9.
Papadopoulou-Legbelou K, Triantafyllou A, Vampertzi O, Koletsos N, Douma S, Papadopoulou-Alataki E
Pulse (Basel)
. 2022 Jan;
9(3-4):64-71.
PMID: 35083172
Background And Aims: This study investigated the possible correlation between elevated lipoprotein (a) (Lp(a)) levels and early vascular aging biomarkers in healthy children and adolescents. Methods: Twenty-seven healthy children/adolescents, mean...
10.
Vampertzi O, Papadopoulou-Legbelou K, Triantafyllou A, Koletsos N, Alataki S, Douma S, et al.
Rheumatol Int
. 2021 Nov;
42(1):59-69.
PMID: 34739572
Familial Mediterranean Fever (FMF) is the most frequent autoinflammatory disease. This study aimed to evaluate the risk of subclinical vascular damage in FMF children, and young adults, using both imaging...