Browsing by Keywords "μεσογειακή αναιμία"

Now showing items 1-7 of 7

  • Nutritional problems of patients with B-Thalassemia: Investigating nutritional kowledge in a patient sample.

    T.E.I. of Crete, School of Agriculture, Food and Nutrition (STeGTET), Department of Nutrition and Dietetics
    Authors: Vasilantonaki, Theopoula
    Thesis advisor: Sfakianaki, Eirini
    Publication Date: 2017-12-05
    Cooley's disease or β-thalassemia is among the most common hereditary diseases of the blood. About 1.5% of the world's population is carriers of β-thalassemia. Patients with β-thalassemia may be at increased risk of eating ...

  • Investigation of compliance of thalassemia patients in Crete on the proposed guidelines and living conditions. Health education in thalassemia.

    T.E.I. of Crete, School of Health and Welfare Services (SEYP), Nursing Department
    Authors: Amyrialaki, Maria; Leraki, Dimitra; Sifalaki, Ioulia-Nektaria
    Thesis advisor: Zografakis-Sfakianakis, Michail
    Publication Date: 29-09-2010

  • Research on the quality of life level and psychological burden of people suffering from thalassemia.

    T.E.I. of Crete, School of Health and Welfare Services (SEYP), Nursing Department
    Authors: Giannadaki, Georgia-Konstantina; Spontidaki, Andromachi; Tzagkaraki, Marilena
    Thesis advisor: Rikos, Nikolaos
    Publication Date: 2018-12-27
    Thalassemia is one of the most common genetic disorders and therefore considered to be a serious issue as far as public health is concerned in the region of the Mediterranean. In such chronic conditions survival and ...

  • Thalassemias and modern treatment.

    T.E.I. of Crete, School of Health and Welfare Services (SEYP), Nursing Department
    Authors: Mpaliou, Marouso; Nikolidaki, Eirini; Tsagkouli, Maria
    Thesis advisor: Darivianaki, Eleutheria
    Publication Date: 29-02-2008

  • 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 ...