Search Results - "Tzouvara, E."

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    A single-center, retrospective study of management and outcome of 45 elderly AML patients, diagnosed in 2001 by Alymara, V, Tzouvara, E, Vartholomatos, G, Chaidos, A, Tsiara, St, Bourantas, K L

    “…Acute myeloid leukemia (AML) predominantly affects older adults, a population with a poor prognosis, due to age, comorbidities and forms of disease. We present…”
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    Journal Article
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    Antierythropoietin antibodies in thalassemia patients by Voulgari, P V, Chaidos, A, Tzouvara, E, Alymara, V, Alamanos, Y, Drosos, A A, Bourantas, K L

    Published in Annals of hematology (01-01-2004)
    “…We evaluated sera from 58 thalassemic patients for the presence of antierythropoietin antibodies to investigate whether these autoantibodies may relate with…”
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    Alemtuzumab 20 mg only in vivo confers efficient GvHD prophylaxis in sibling and matched unrelated HCT by Spyridonidis, A, Karakantza, M, Symeonidis, A, Triantafyllou, E, Tzouvara, E, Kourakli, A, Tiniakou, M, Zoumbos, N

    Published in Bone marrow transplantation (Basingstoke) (01-03-2009)
    “…Despite standard CyA/MTX GvHD prophylaxis, severe acute GVHD occurs after ~35% of matched sibling HCT. MTX is associated with mucositis, delayed engraftment…”
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    Solitary extramedullary plasmacytoma of the maxillary sinus. Case report by Exarchakos, G, Korantzopoulos, P, Bai, M, Xanthopoulos, J, Tzouvara, E, Skevas, A

    “…Solitary extramedullary plasmacytomas are rare tumors that often affect head and neck region. Because of the non-specific associated symptomatology, they…”
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    Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules by Chaidos, Aristeidis, Makis, Alexandros, Hatzimichael, Eleftheria, Tsiara, Stavroula, Gouva, Maria, Tzouvara, Evangelia, Bourantas, Konstantinos L

    Published in Acta haematologica (01-01-2004)
    “…The most common single genetic disorder and a major public health issue in Greece and other Mediterranean countries is beta-thalassemia. Current therapeutic…”
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