Athanasios Anastasiadis

ORCID: 0000-0003-1873-3491
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About
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Research Areas
  • Contemporary and Historical Greek Studies
  • Chronic Lymphocytic Leukemia Research
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Immunodeficiency and Autoimmune Disorders
  • Byzantine Studies and History
  • Hemoglobinopathies and Related Disorders
  • Eosinophilic Disorders and Syndromes
  • Acute Myeloid Leukemia Research
  • Blood groups and transfusion
  • Biosimilars and Bioanalytical Methods
  • Multiple Myeloma Research and Treatments
  • Balkans: History, Politics, Society
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Iron Metabolism and Disorders
  • Identification and Quantification in Food
  • Marine Ecology and Invasive Species
  • Balkan and Eastern European Studies
  • Lymphoma Diagnosis and Treatment
  • Cytokine Signaling Pathways and Interactions
  • Erythrocyte Function and Pathophysiology
  • European history and politics
  • European Monetary and Fiscal Policies
  • Identity, Memory, and Therapy
  • Blood disorders and treatments
  • Housing, Finance, and Neoliberalism

Papageorgiou General Hospital
2024

University of Patras
2021-2023

G. Papanikolaou General Hospital
2021

University Hospital of Alexandroupolis
2011-2018

Universität Hamburg
2011

Democritus University of Thrace
2006-2009

We analyzed the expression of CD1d, an antigen-presenting molecule, on peripheral blood leukemic cells cases chronic lymphocytic leukemia (CLL) by flow cytometry. demonstrated variable CD1d lymphocytes and association between high with shorter time to treatment overall survival patients. was positively associated CD38 expression, but not unmutated heavy chain (VH) mutational status or adverse cytogenetics lymphocytes. Our findings support that is a prognostic marker for CLL.

10.3109/10428194.2013.803222 article EN Leukemia & lymphoma/Leukemia and lymphoma 2013-05-14

Hyperhemolytic Syndrome or Transfusion Reaction (HHTR), a life-threatening subset of Delayed Hemolytic (DHTR) is characterized by destruction both transfused and autologous erythrocytes evidenced fall in post transfusion hemoglobin below the pre-transfusion level.We describe case DHTR due to anti-P1 alloimmunization manifesting with hyperhemolysis 30-year-old Greek Pomak woman thalassemia intermedia (HbO-Arab/β-thalassemia), during the11th week her first gestation. She was successfully...

10.4084/mjhid.2016.053 article EN cc-by-nc Mediterranean Journal of Hematology and Infectious Diseases 2016-10-18

Furthermore, AG has no myelotoxic or leukemogenic potential to add that of HU. Based on these considerations, we reviewed the records patients with PV ET treated in our institution and analyzed characteristics those HU plus order assess feasibility combination terms efficacy safety. We identified 16 cases which a had been used at some point their course between June 2003 February 2008. Diagnosis was made according WHO criteria for ET, idiopathic myelofibrosis (IM). Thirteen were investigated...

10.1159/000189381 article EN Acta Haematologica 2008-01-01

Chondrichthyans are apex predators influencing the trophic web through a top-down process thus their depletion will affect remaining biota. Notwithstanding that, research on chondrichthyans is sparse or data-limited in several biogeographic areas worldwide, including Levantine Sea. We revise and update knowledge of Cyprus based bibliographic review that gains information retrieved from peer-reviewed grey literature, Global Biodiversity Information Facility (135 records at least 18 species)...

10.3390/fishes6030024 article EN cc-by Fishes 2021-07-26

10.1515/jlt-2011-0005 article EN Journal of Literary Theory 2012-01-01

It has been proposed that vitamin D may play a role in prevention and treatment of cancer while epidemiological studies have linked insufficiency to adverse disease outcomes various B cell malignancies, including chronic lymphocytic leukemia (CLL). In this study, we sought obtain deeper biological insight into the its receptor (VDR) pathophysiology CLL. To end, performed expression analysis pathway molecules; complemented by RNA-Sequencing primary CLL cells were treated vitro with...

10.3390/cancers13020285 article EN Cancers 2021-01-14

In recent years, the trauma concept has been applied to fiction in several literary studies. This article discusses narrative mediation of traumatic experiences selected Civil War novels, using narratological tools and focusing on complex relationship between trauma, memory narration. The authors use innovative representational strategies, such as a disrupted chronological order or intertextual references, illustrate paradoxical character remembering narrating trauma. These works highlight...

10.1179/030701311x12906801091674 article EN Byzantine and Modern Greek Studies 2011-01-01

Acquired pure red cell aplasia is a rare disorder, usually appearing secondary to various pathologic conditions such as thymoma, systemic autoimmune diseases or in the course of lymphomas. Conventional treatment consists immunosuppression with corticosteroids, antithymocyte globulin cyclosporin-A. 8 weekly courses rituximab were administered patient who presented newly diagnosed splenic marginal zone lymphoma. Transfusion independence was achieved after 6th course, and receded completely...

10.4076/1757-1626-2-6913 article EN cc-by Cases Journal 2009-01-01

<i>Background:</i> Farnesyltransferase inhibitors (FTIs) target proteins needing prenylation for functioning. Tipifarnib (Zarnestra®), a potent and specific inhibitor of farnesyltransferase, showed considerable activity in phase I II studies myelodysplastic syndrome (MDS), but the optimal regimen achieving high response rates with minor myelosuppression remains to be determined. Additionally, direct effect on purified human MDS progenitors has not yet been shown.<i>...

10.1159/000158577 article EN Acta Haematologica 2008-01-01

<i>Background/Aims:</i> Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs) share the same acquired lesion JAK2<sup>V617F</sup> and may exhibit substantial overlap. Variability in JAK activation allele burden, complemented by host, genetic non-genetic modifiers, determine phenotype. The aim of this study was to investigate presence JAK2 mutation association with ratio metallopeptidases inhibitors (TIMPs) tissue (MMPs) MPNs, where inhibitory rather...

10.1159/000324436 article EN Acta Haematologica 2011-01-01

Abstract Background: Hyperhemolytic Syndrome or Transfusion Reaction (HHTR), a life-threatening subset of Delayed Hemolytic (DHTR) is characterized by destruction both transfused and autologous erythrocytes evidenced fall in post transfusion hemoglobin below the pre-transfusion level.Case report: We describe case DHTR due to anti-P1 alloimmunization manifesting with hyperhemolysis 30-year-old Greek Pomak woman thalassemia intermedia (HbO-Arab/β-thalassemia), during the11th week her first...

10.4084/mjhid.2016.53 article EN cc-by-nc Mediterranean Journal of Hematology and Infectious Diseases 2016-10-18

The above authors remove these recent publications due to remaining uncertainty because they are based on a visual observation by citizen (citizen science), without specimen being available. available information was not adequate support this record solely photographic evidence and direct contact between the citizen.

10.12681/mms.34033 article EN cc-by-nc Mediterranean Marine Science 2023-03-22
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