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International Journal of Hematology|February 8, 2014
Concurrent presentation of nodal myeloid sarcoma and bone marrow chronic lymphocytic leukemia/small lymphocytic lymphoma: a unique associationVasilios Perifanis, Michael D Diamantidis, Kyriaki Chalvatzi, et al.
Hematology Reports|August 22, 2023
Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature ReviewMichael D Diamantidis, Stefania Pitsava, Omar Zayed, et al.
Acta Haematologica|January 4, 2011
Aggressive systemic mastocytosis associated with mesangioproliferative glomerulonephritisMichael D Diamantidis, Athena D Myrou, Georgia D Kaiafa, et al.
International Journal of Hematology|June 24, 2009
Differential diagnosis and treatment of primary, cutaneous, anaplastic large cell lymphoma: not always an easy taskMichael D Diamantidis, Athanasios Papadopoulos, Georgia Kaiafa, et al.
Acta Haematologica|October 13, 2010
High prevalence of Helicobacter pylori infection in Greek patients with myelodysplastic syndromesMichael D Diamantidis, Elizabeth Ioannidou-Papagiannaki, Jannis Kountouras, et al.
Ejhaem|August 21, 2023
Real-world complication burden and disease management paradigms in transfusion-related β-thalassaemia in Greece: Results from ULYSSES, an epidemiological, multicentre, retrospective cross-sectional studyAntonis Kattamis, Ersi Voskaridou, Sophia Delicou, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 7, 2023
Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotypeMichael D Diamantidis, Rebecca-Anastasia Karanikola, Chrysoula Polyzoudi, et al.
Blood Advances|June 4, 2026
Phase 2a randomized study to evaluate sapablursen in patients with non-transfusion dependent β-thalassemia intermediaAli Taher, Michael D Diamantidis, Antonis Kattamis, et al.
British Journal of Haematology|March 16, 2025
Comparative analysis of mortality patterns and treatment strategies in thalassaemia and sickle cell disease patients: A 12-year studySophia Delicou, Konstantinos Manganas, Michael D Diamantidis, et al.
Orphanet Journal of Rare Diseases|April 16, 2025
COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNetPablo Velasco Puyo, Soteroula Christou, Saveria Campisi, et al.
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