Browsing EΛ.ΜΕ.ΠΑ. / HMU by Keywords "thalassemia"

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  • Factors associated with the quality of life of patients with thalassaemia.

    Η.Μ.U, School of Health Sciences (SHS), Social Work Dept.
    Authors: Spantidaki, Eirini
    Thesis advisor: Koukouli, Sofia
    Publication Date: 2022-03-29
    The purpose of this study is to understand the factors related to the quality of life of people with thalassemia, for example: a) if they have acquired changes in their appearance and if this makes them feel different from ...

  • Quality of life of people with homozygous major β-thalassemia in Europe.

    Η.Μ.U, School of Health Sciences (SHS), Nursing Dept.
    Authors: Diarmisi, Styliani; Tsikritsakis, Nikolaos
    Thesis advisor: Christodoulakis, Antonios
    Publication Date: 2021-09-20
    Introduction: Thalassemia is one of the most common hematological hereditary diseases worldwide. It manifests itself in two forms, homozygous and heterozygous bMediterranean Anemia. The homozygous β- M.A. affects the ...

  • Μost frequent complications of patients with Mediterranean anemia.

    Η.Μ.U, School of Health Sciences (SHS), Nursing Dept.
    Authors: Nikoli, Nikoletta-Parthena; Trypidaki, Georgia; Chatzidakis, Spyros
    Thesis advisor: Rikos, Nikolaos
    Publication Date: 2022-10-27
    Introduction: Thalassaemias are inherited hemolytic anemias with autosomal recessive heredity characterized by the inability to produce one or more globin chains that form a hemoglobin molecule. Regular blood transfusions ...