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Acta Dermato-Venereologica|June 5, 2023
Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek ChildrenLamprini Nasi, Alexios Alexopoulos, Eleftheria Kokkinou, et al.
Current Molecular Medicine|March 15, 2019
Bone Metabolism Markers in Thalassemia Major-Induced Osteoporosis: Results from a Cross-Sectional Observational StudyAthanasios N Tsartsalis, George I Lambrou, Dimitrios N Tsartsalis, et al.
Haematologica|January 15, 2026
Abrupt ferritin increases as a marker of cancer in transfusion-dependent thalassemiaElena Chatzikalil, Polyxeni Delaporta, Ilona Binenbaum, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 24, 2005
R2 relaxometry with MRI for the quantification of tissue iron overload in beta-thalassemic patientsEfthymia Alexopoulou, Fotini Stripeli, Panagiotis Baras, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 17, 2013
Pituitary stalk lesion in a 13-year-old femaleMihail Zilbermint, Mary S Ramnitz, Maya B Lodish, et al.
Cureus|July 28, 2025
Deciphering Atypical Signals Present in Fluorescent In Situ Hybridization Assays in the Diagnosis of Soft Tissue SarcomasAlexandra B Papakosta, Louisa G Mahaira, Eftimios S Dimitriadis, et al.
Children (Basel, Switzerland)|July 29, 2023
A Novel Variant in the TP53 Gene Causing Li-Fraumeni SyndromeDimitrios T Papadimitriou, Constantine A Stratakis, Antonis Kattamis, et al.
Clinical Immunology (Orlando, Fla.)|June 3, 2023
Evidence that platelets from transfusion-dependent β-thalassemia patients induce T cell activationElena E Solomou, Polyxeni Delaporta, Aimilia Mantzou, et al.
Systems Biology in Reproductive Medicine|December 5, 2015
Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typingGeorgia Kakourou, Christina Vrettou, Antonis Kattamis, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 16, 2008
Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletionJoaquim Calado, Yves Sznajer, Daniel Metzger, et al.
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