Kyriaki Legbelou-Papadopoulou

Thessaloniki, ESYE12, Greece

Last Updated: 09/26/2026

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Found 28 publications

An Outbreak of Myocarditis and Asymptomatic Troponinemia in Children Following Parvovirus B19 Infections in Northern Greece and a Scoping Review.

An Outbreak of Myocarditis and Asymptomatic Troponinemia in Children Following Parvovirus B19 Infections in Northern Greece and a Scoping Review.

Journal: The Pediatric infectious disease journal

Published: January 14, 2026

Severe tortuosity but not altered retinal vessel diameters in children and young adults with Familial Mediterranean Fever: a case-control study.

Severe tortuosity but not altered retinal vessel diameters in children and young adults with Familial Mediterranean Fever: a case-control study.

Journal: Rheumatology international

Published: January 07, 2026

Subclinical Myocardial Dysfunction in Pediatric and Adolescent Celiac Disease Patients: A Systematic Review and Meta-Analysis.

Subclinical Myocardial Dysfunction in Pediatric and Adolescent Celiac Disease Patients: A Systematic Review and Meta-Analysis.

Journal: Children (Basel, Switzerland)

Published: January 09, 2025

A 17-month-old girl with fetal valproate syndrome and ocular coloboma.

A 17-month-old girl with fetal valproate syndrome and ocular coloboma.

Journal: Clinical dysmorphology

Published: February 27, 2024

Multisystem inflammatory syndrome in children (MIS-C): A nationwide collaborative study in the Greek population.

Multisystem inflammatory syndrome in children (MIS-C): A nationwide collaborative study in the Greek population.

Journal: European journal of pediatrics

Published: August 10, 2023

Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome.

Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome.

Journal: Case reports in genetics

Published: June 12, 2023

Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene.

Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene.

Journal: American journal of medical genetics. Part A

Published: June 09, 2023

A pediatric case of atypical hemolytic uremic syndrome (aHUS): Could any infection play a triggering role?

A pediatric case of atypical hemolytic uremic syndrome (aHUS): Could any infection play a triggering role?

Journal: Clinical nephrology. Case studies

Published: May 22, 2023

Beckwith-Wiedemann syndrome with multiple hepatic and cutaneous hemangiomas in a female patient of Albanian origin: Diagnostic and therapeutic considerations.

Beckwith-Wiedemann syndrome with multiple hepatic and cutaneous hemangiomas in a female patient of Albanian origin: Diagnostic and therapeutic considerations.

Journal: American journal of medical genetics. Part A

Published: February 06, 2023

Decreasing Incidence of the Multisystem Inflammatory Syndrome in Children Over 3 Pandemic Waves.

Decreasing Incidence of the Multisystem Inflammatory Syndrome in Children Over 3 Pandemic Waves.

Journal: The Pediatric infectious disease journal

Published: January 13, 2023

Association of rs738409 Polymorphism in Adiponutrin Gene with Liver Steatosis and Atherosclerosis Risk Factors in Greek Children and Adolescents.

Association of rs738409 Polymorphism in Adiponutrin Gene with Liver Steatosis and Atherosclerosis Risk Factors in Greek Children and Adolescents.

Journal: Nutrients

Published: July 17, 2022

Multisystem inflammatory syndrome in a child with low inflammatory markers, persistent hyponatremia, and natriuresis.

Multisystem inflammatory syndrome in a child with low inflammatory markers, persistent hyponatremia, and natriuresis.

Journal: Hippokratia

Published: April 01, 2022

Showing 1-12 of 28

Last Updated: 09/26/2026