Polyxeni Delaporta

National and Kapodistrian University of Athens — Greece

Medicine · Health Sciences

10h-index288citations58works0.72yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(40), Iron Metabolism and Disorders(19), Blood groups and transfusion(12), Cancer-related gene regulation(7), RNA modifications and cancer(6)

Publications57 total

Romosozumab for the treatment of thalassemia-associated osteoporosis in two female patients
JBMR Plus·2026Open Access
Abrupt ferritin increases as a marker of cancer in transfusion-dependent thalassemia
Haematologica·2026Open Access
The ‘αO2-PRBCThal’ trial on the use of hemanext One® for blood transfusion support transfusion-dependent thalassemia
Blood·2025
Assessment of the angiogenic proteins placental growth factor (PlGF) and soluble fms-like tyrosine kinase 1 (sFlt-1) in patients with hereditary spherocytosis
Blood·2025Open Access
Low hematologic event-free survival with age in shwachman-diamond syndrome
Blood·2025
The international diamond blackfan anemia syndrome cancer consortium: Preliminary results
Blood·2025
Oral glucose tolerance test remains the gold standard for diagnosis of glucose metabolism disturbances in thalassemia patients
Blood·2025Open Access
COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet
Orphanet Journal of Rare Diseases·2025Open Access
Comparative analysis of mortality patterns and treatment strategies in thalassaemia and sickle cell disease patients: A 12‐year study
British Journal of Haematology·2025· 4 citedOpen Access
Incidence of Myeloid Malignancy in Shwachman-Diamond Syndrome: An International Cohort Study
Blood·2024· 1 citedOpen Access
Abrupt Increases in Ferritin Levels May Indicate a Malignant Process and Not Changes in Iron Overload in Thalassemic Patients
Blood·2024· 3 cited
COVID-19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet
2024Open Access
Lethal Complications and Complex Genotypes in Shwachman Diamond Syndrome: Report of a Family with Recurrent Neonatal Deaths and a Case-Based Brief Review of the Literature
Children·2024· 1 citedOpen Access
Evolving Changes in the Characteristics of Death in Transfusion Dependent Thalassemia in Greece
Blood·2023· 4 cited
A multicenter ICET-A study on age at menarche and menstrual cycles in patients with transfusion-dependent thalassemia (TDT) who started early chelation therapy with different chelating agents
Mediterranean Journal of Hematology and Infectious Diseases·2023· 2 citedOpen Access
PB2532: VARIABLE HEMATOLOGICAL AND CLINICAL PHENOTYPES IN DOUBLE HETEROZYGOTES OF ΒETA-THALASSEMIA AND TRIPLICATED ΑLPHA-GLOBIN GENES
HemaSphere·2023Open Access
P795: NEUTROPENIA IN CHILDHOOD IS MOST FREQUENTLY DUE TO AN AUTOIMMUNE PROCESS AND HAS A BENIGN COURSE.
HemaSphere·2023Open Access
P798: DIAMOND BLACKFAN ANEMIA MAY ESCAPE DIAGNOSIS UP TO ADULTHOOD; A REPORT FROM THE UPDATED GREEK REGISTRY
HemaSphere·2023Open Access
Evidence that platelets from transfusion-dependent β-thalassemia patients induce T cell activation
Clinical Immunology·2023
Real-World Data on the Use of Luspatercept in Greek Patients with Transfusion Dependent Thalassemia
Blood·2022· 5 cited
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Frequent Co-authors

Antonis Kattamis(34), Ioannis Papassotiriou(18), Dimitra Kyriakopoulou(11), Antonios Kattamis(10), Christalena Sofocleous(7), Michael D. Diamantidis(7), Christos Kattamis(6), Saveria Campisi(6), Filia Apostolakou(5), Marina Economou(5), Elena E. Solomou(5), Konstantina Toutoudaki(5), Pagona Flevari(5), Stavroula Kostaridou(4), Elena Chatzikalil(4), Pablo Velasco(4), Tatiana Besse‐Hammer(4), Simona Raso(4), Anna Spasiano(4), Laurence Dedeken(4)