Search Results - "Kattamis, Antonios"

Refine Results
  1. 1

    Invasive Fungal Infections in Children with Haematological Malignancies: Diagnostic and Therapeutic Challenges by Tragiannidis, Athanasios, Kattamis, Antonios, Vyzantiadis, Timoleon-Achilleas

    Published in Journal of fungi (Basel) (28-06-2021)
    “…The incidence of invasive fungal infections (IFIs) has dramatically increased over the last few decades in parallel with the increased number of…”
    Get full text
    Journal Article
  2. 2
  3. 3
  4. 4
  5. 5

    Low- and High-Attenuation Lung Volume in Quantitative Chest CT in Children without Lung Disease by Moutafidis, Dimitrios, Gavra, Maria, Golfinopoulos, Sotirios, Kattamis, Antonios, Chrousos, George, Kanaka-Gantenbein, Christina, Kaditis, Athanasios G

    Published in Children (Basel) (10-12-2021)
    “…In contrast to studies of adults with emphysema, application of fixed thresholds to determine low- and high-attenuation areas (air-trapping and parenchymal…”
    Get full text
    Journal Article
  6. 6
  7. 7
  8. 8
  9. 9

    Pregnancy Complications in a-Thalassemia (Hemoglobinopathy H): A Case Study by Vlahos, Nikos F., Tsaroucha, Athanasia, Triantafyllou, Faidra-Evangelia, Valsami, Serena, Efstathopoulou, Maria, Dryllis, Giorgos, Politou, Marianna, Kattamis, Antonis

    “…Thalassemia intermedia (TI) is a clinical definition which represents a wide spectrum of thalassemia genotypes but mainly includes patients who do not require…”
    Get full text
    Journal Article
  10. 10

    Predisposing factors for advanced liver fibrosis in patients with sickle cell disease by Manganas, Konstantinos, Delicou, Sophia, Xydaki, Aikaterini, Kourakli, Alexandra, Evliati, Loukia, Vlachaki, Efthymia, Klironomos, Evangelos, Diamantidis, Michail, Lafiatis, Ioannis, Kattamis, Antonios, Koskinas, John

    Published in British journal of haematology (01-09-2023)
    “…Sickle cell disease (SCD) is one of the most common monogenic disorders worldwide and liver complications are common in this group of patients. Our study aims…”
    Get full text
    Journal Article
  11. 11

    Abdominal ultrasonographic findings in patients with sickle-cell anaemia and thalassaemia intermedia by PAPADAKI, Marina G, KATTAMIS, Antonios C, PAPADAKI, Irene G, MENEGAS, Damianos G, GEORGAKOPOULOU, Theano P, MAVROMMATI-METAXOTOU, Anna, KATTAMIS, Christos A

    Published in Pediatric radiology (01-08-2003)
    “…The high prevalence and heterogeneity of clinical and haematological phenotypes of sickle-cell anaemia and thalassaemia intermedia (TI) syndromes in the Greek…”
    Get full text
    Journal Article
  12. 12
  13. 13
  14. 14

    Increased T Follicular Helper Cells in Patients with Aplastic Anemia by Verigou, Evgenia, Galanopoulos, Athanasios, Kattamis, Antonios, Symeonidis, Argiris, Solomou, Elena E.

    Published in Blood (02-12-2016)
    “…Introduction:T-follicular helper cells represent a sub-population of CD4+helper T cells (TFH), and they are characterized by the surface expression of CXCR5,…”
    Get full text
    Journal Article
  15. 15

    The Effect of Hepatitis C - Direct-Acting Antiviral Treatment on the Hematogical Profile of Thalassemic Patients by Bristogiannis, Sotirios, Kattamis, Antonios, Kyriakopoulou, Dimitra, Moraki, Maria, Kountouras, Dimitrios, Alexiou, Nikolaos

    Published in Blood (02-12-2016)
    “…Background: The prevalence ofhepatitis C (HCV) infection remains high among transfusion-dependent thalassemic patients. Chronic Hepatitis C, along with iron…”
    Get full text
    Journal Article
  16. 16
  17. 17
  18. 18
  19. 19

    Neutrophil Gelatinase-Associated Lipocalin Levels in Patients with Thalassemia and Sickle Cell Disease: Correlation with Renal Injury by Papassotiriou, Ioannis, Ersi, Voskaridou, Margeli, Alexandra, Nwagha, Theresa, Kotrotsou, Athanassia, Kyriakopoulou, Dimitra, Poziopoulos, Christos, Kattamis, Antonios

    Published in Blood (06-12-2014)
    “…Background and Aims: Neutrophil gelatinase-associated lipocalin (NGAL) is a protein belonging to the lipocalin superfamily initially found in activated…”
    Get full text
    Journal Article
  20. 20

    Combination Therapy of Deferasirox and Deferoxamine As Paregoric Treatment of Severe Iron Overload in Patients with Thalassemia Major by Ladis, Vassilis, Kyriacopoulou, Dimitra, Stokidis, Konstantinos, Moira, Aggeliki, Kattamis, Antonios

    Published in Blood (16-11-2012)
    “…Abstract 5181 Despite the recent availability of multiple therapeutic options for chelation therapy, severe iron overload remains a significant cause of…”
    Get full text
    Journal Article