Paraskevi Papadogeorgou

Neonatal Sepsis-Induced Coagulopathy in the Light of Developmental Hemostasis: Friend or Foe?

Paraskevi Papadogeorgou, Rozeta Sokou, Sotirios P. Fortis, Vasiliki Mougiou et autres

The concept of 'developmental hemostasis' from birth to infancy and onwards to childhood and adulthood was introduced in the 1980s and is used to indicate the fundamental discrepancies of hemostatic mechanism between children and adults. The underlying differentiations are more pronounced in …

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Coagulation Profile in Neonates with Congenital Heart Disease: A Pilot Study

Paraskevi Papadogeorgou, Serena Valsami, Maria Boutsikou, Helen Pergantou et autres

Background and Objectives: congenital heart disease (CHD), cyanotic and, to a lesser degree, acyanotic, often are accompanied by coagulation abnormalities, impacting substantially morbidity and mortality. Until now, no consistent hemostatic patterns have been demonstrated in neonates and children with CHD because they …

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A Global Assessment of Coagulation Profile and a Novel Insight into Adamts-13 Implication in Neonatal Sepsis

Paraskevi Papadogeorgou, Τheodora Boutsikou, Maria Boutsikou, Eleni Pergantou et autres

Neonatal sepsis is a life-threatening condition associated with significant morbidity and mortality. Sepsis-induced coagulopathy is a well-recognized entity, signifying the strong cross-talk between inflammation and coagulation. The aim of the present study was to compare the coagulation profile between the acute phase …

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Epidemiology and Risk Factors for Coronary Artery Abnormalities in Children With Complete and Incomplete Kawasaki Disease During a 10-Year Period

Georgia Giannouli, Chryssa Tzoumaka‐Bakoula, Ioannis Kopsidas, Paraskevi Papadogeorgou et autres

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Chylomicron retention disease: report of two cases from a Greek Island

Paraskevi Papadogeorgou, Elefthería Roma, Agnès Sassolas, Irene Orfanou et autres

Chylomicron retention disease (CRD), or Anderson disease, is a rare, hereditary cause of fat malabsorption. It is one of the familial hypocholesterolaemia syndromes, along with homozygous hypobetalipoproteinaemia (HBL) and abetalipoproteinaemia (ABL). We report clinical, laboratory and histological data as well as molecular …

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