Search Results - "Delaporta, Polyxeni"

Serum Levels of S100b and NSE Proteins in Patients with Non-Transfusion-Dependent Thalassemia as Biomarkers of Brain Ischemia and Cerebral Vasculopathy by Kanavaki, Aikaterini, Spengos, Konstantinos, Moraki, Maria, Delaporta, Polyxeni, Kariyannis, Catherine, Papassotiriou, Ioannis, Kattamis, Antonis

“…Patients with non-transfusion-dependent thalassemia (NTDT) are at risk of developing brain ischemia. Transcranial Doppler (TCD) has been established as a…”
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Genotype-phenotype association and variant characterization in Diamond-Blackfan anemia caused by pathogenic variants in RPL35A by Gianferante, Matthew D, Wlodarski, Marcin W, Atsidaftos, Evangelia, Da Costa, Lydie, Delaporta, Polyxeni, Farrar, Jason E, Goldman, Frederick D, Hussain, Maryam, Kattamis, Antonis, Leblanc, Thierry, Lipton, Jeffrey M, Niemeyer, Charlotte M, Pospisilova, Dagmar, Quarello, Paola, Ramenghi, Ugo, Sankaran, Vijay G, Vlachos, Adrianna, Volejnikova, Jana, Alter, Blanche P, Savage, Sharon A, Giri, Neelam

“…Diamond Blackfan anemia (DBA) is predominantly an autosomal dominant inherited red cell aplasia primarily caused by pathogenic germline variants in ribosomal…”
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P795: NEUTROPENIA IN CHILDHOOD IS MOST FREQUENTLY DUE TO AN AUTOIMMUNE PROCESS AND HAS A BENIGN COURSE by Toutoudaki, Konstantina, Solomou, Elena, Delaporta, Polyxeni, Bregova, Ioanna, Binenbaum, Ilona, Tzanoudaki, Marianna, Kattamis, Antonis

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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 by Veltra, Danai, Marinakis, Nikolaos M, Kotsios, Ioannis, Delaporta, Polyxeni, Kekou, Kyriaki, Kosma, Konstantina, Traeger-Synodinos, Joanne, Sofocleous, Christalena

“…Shwachman Diamond Syndrome (SDS) is a multi-system disease characterized by exocrine pancreatic insufficiency with malabsorption, infantile neutropenia and…”
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Left ventricular deformation mechanics over time in patients with thalassemia major with and without iron overload by Bonios, Michael J, Fountas, Epameinontas, Delaporta, Polyxeni, Kyrzopoulos, Stamatis, Kattamis, Antonis, Adamopoulos, Stamatis N, Tsiapras, Dimitris

“…Myocardial iron overload in patients with thalassemia major (TM) is one of the most important complications. The purpose of the study was to identify advanced…”
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Heterozygosity of the Complex Corfu δ0β+ Thalassemic Allele (HBD Deletion and HBB:c.92+5G>A) Revisited by Kattamis, Christos, Skafida, Myrto, Delaporta, Polyxeni, Vrettou, Christina, Traeger-Synodinos, Joanne, Sofocleous, Christalena, Kattamis, Antonis

“…The Corfu δ β thalassemic allele is a unique thalassemic allele consisting of the simultaneous presence in cis of a deletion of the δ-globin (Hemoglobin…”
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PB2532: VARIABLE HEMATOLOGICAL AND CLINICAL PHENOTYPES IN DOUBLE HETEROZYGOTES OF ΒETA‐THALASSEMIA AND TRIPLICATED ΑLPHA‐GLOBIN GENES by Delaporta, Polyxeni, Vrettou, Christina, Chouliara, Vasiliki, Chatzieleftheriou, Maria‐Ioanna, Kyriakopoulou, Dimitra, Moraki, Maria, Traeger‐Synodinos, Joanne, Kattamis, Antonis

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P798: DIAMOND BLACKFAN ANEMIA MAY ESCAPE DIAGNOSIS UP TO ADULTHOOD; A REPORT FROM THE UPDATED GREEK REGISTRY by Delaporta, Polyxeni, Sofocleous, Christalena, Glentis, Stavros, Veltra, Danai, Polychronopoulou, Sophia, Kossiva, Lydia, Makis, Alexandros, Economou, Marina, Katzilakis, Nikolaos, Steiakaki, Eftychia, Marinakis, Theodoros, Kostaridou, Stavroula, Kattamis, Antonis

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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 by Di Maio, Salvatore, Marzuillo, Pierluigi, Daar, Shahina, Kattamis, Christos, Karimi, Mehran, ough, Saki, Banchev, Atanas, Kaleva, Valeria, Christou, Soteroula, tugno, Carmelo, Delaporta, Polyxeni, Soliman, Ashraf T, Tzoulis, Ploutarchos, de Sanctis, Vincenzo

“…IntroductionTo evaluate the effect of early chelation therapy (≤ 3 years) with a variety of chelating agents on age at menarche and menstrual characteristics…”
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Evolving Changes in the Characteristics of Death in Transfusion Dependent Thalassemia in Greece by Delaporta, Polyxeni, Chatzikalil, Elena, Ladis, Vassilis, Moraki, Maria, Kattamis, Antonis

“…Introduction: During the last decades, improvements in the treatment of transfusion-dependent thalassemia (TDT) with safer transfusion schemas, improved…”
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Diamond-Blackfan Anemia: 2 Cases With a Twist by Kossiva, Lydia, Markande, Aikaterini, Vagianou, Fotini, Delaporta, Polyxeni, Kattamis, Antonis

“…Diamond-Blackfan anemia is a rare inherited bone marrow failure disease. Typical findings include hypoplastic macrocytic anemia, congenital anomalies, and a…”
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Adverse Events Following COVID-19 Vaccination in Transfusion-Dependent -Thalassemia Patients by Delaporta, Polyxeni, Lampropoulou, Eugenia, Moschoviti, Anastasia, Binenbaum, Ilona, Kyriakopoulou, Dimitra, Ioakeimidou, Natalia, Chante, Sofia, Papassotiriou, Ioannis, Kattamis, Antonis

“…Patients with transfusion-dependent-thalassemia (TDT) are considered as increased risk population for severe and/or morbid COVID-19 infection. Timely…”
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Evidence That Platelets from Transfusion-Dependent Thalassemia Patients Induce T Cell Activation by Solomou, Elena E., Delaporta, Polyxeni, Mantzou, Aimilia, Tzannoudaki, Marianna, Diamantopoulos, Panagiotis T, Salamaliki, Christina, Kontandreopoulou, Christina-Nefeli, Vyniou, Athina, Perganti, Foteini, Papassotiriou, Ioannis, Kattamis, Antonis

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High Incidence of Clonal Hematopoiesis in Transfusion-Dependent Thalassemia Patients by Solomou, Elena E., Delaporta, Polyxeni, Stamatia, Laidou, Katsika, Efthymia-Vasilina, Chatzieleftheriou, Marianna, Toutoudaki, Konstantina, Glentis, Stavros, Stamatopoulos, Kostas, Chatzidimitriou, Anastasia, Kattamis, Antonis

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The Greek Registry of Shwachman Diamond‐Syndrome: Molecular and clinical data by Delaporta, Polyxeni, Sofocleous, Christalena, Economou, Marina, Makis, Alexandros, Kostaridou, Stavroula, Kattamis, Antonis

“…This study presents the clinical phenotype and molecular analysis findings from 11 patients recorded in the Greek Shwachman–Diamond syndrome (SDS) Registry…”
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Evidence that platelets from transfusion-dependent β-thalassemia patients induce T cell activation by Solomou, Elena E., Delaporta, Polyxeni, Mantzou, Aimilia, Tzannoudaki, Marianna, Diamantopoulos, Panagiotis, Salamaliki, Christina, Kontandreopoulou, Christina-Nefeli, Vyniou, Nora-Athina, Perganti, Foteini, Papassotiriou, Ioannis, Kattamis, Antonis

“…A hypercoagulable state leading to increased risk for thrombotic events represents one of the most common complications observed in transfusion-dependent…”
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Immune response and adverse events after vaccination against SARS‐CoV‐2 in adult patients with transfusion‐dependent thalassaemia by Delaporta, Polyxeni, Terpos, Evangelos, Solomou, Elena E., Gumeni, Sentiljana, Nitsa, Evangelia, Apostolakou, Filia, Kyriakopoulou, Dimitra, Ntanasis‐Stathopoulos, Ioannis, Papassotiriou, Ioannis, Trougakos, Ioannis P., Dimopoulos, Meletios A., Kattamis, Antonis

“…Summary Patients with transfusion‐dependent thalassaemia (TDT) are considered an at increased‐risk population for severe and/or morbid coronavirus disease 2019…”
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Real-World Data on the Use of Luspatercept in Greek Patients with Transfusion Dependent Thalassemia by Delaporta, Polyxeni, Kourakli, Alexandra, Delicou, Sophia, Diamantidis, Michael D., Kalkana, Chrysoula, Vlachaki, Efthymia, Eftychiadis, Eftychios, Lafiatis, Ioannis, Pantelidou, Despoina, Symeonidis, Argiris, Lazaris, Vasileios, Xydaki, Aikaterini, Manafas, Achilles, Evliati, Loukia, Klonizakis, Filippos, Manika, Ioanna, Papadopoulou, Despoina, Chatzieleftheriou, Marianna, Toutoudaki, Konstantina, Kyriakopoulou, Dimitra, Kattamis, Antonis

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PlGF and sFlt‐1 levels in patients with non‐transfusion‐dependent thalassemia: Correlations with markers of iron burden and endothelial dysfunction by Kelaidi, Charikleia, Kattamis, Antonis, Apostolakou, Filia, Poziopoulos, Christos, Lazaropoulou, Christina, Delaporta, Polyxeni, Kanavaki, Ino, Papassotiriou, Ioannis

“…Background Levels of the angiogenic cytokines placental growth factor (PlGF) and soluble Fms‐like tyrosine kinase‐1 (sFlt‐1) and the angiogenic balance,…”
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Pl GF and sF lt‐1 levels in patients with non‐transfusion‐dependent thalassemia: Correlations with markers of iron burden and endothelial dysfunction by Kelaidi, Charikleia, Kattamis, Antonis, Apostolakou, Filia, Poziopoulos, Christos, Lazaropoulou, Christina, Delaporta, Polyxeni, Kanavaki, Ino, Papassotiriou, Ioannis

“…Abstract Background Levels of the angiogenic cytokines placental growth factor (Pl GF ) and soluble Fms‐like tyrosine kinase‐1 ( sF lt‐1) and the angiogenic…”
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