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  • 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 ...