Browsing EΛ.ΜΕ.ΠΑ. / HMU by Keywords "μεσογειακή αναιμία"
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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.
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Publication Date: 2022-03-29The 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.
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Publication Date: 2021-09-20Introduction: 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.
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Publication Date: 2022-10-27Introduction: 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 ...