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Nouvelle Revue Francaise D'Hematologie|January 1, 1983
[Erythrocyte volume and 2,3-DPG level. A study on a primary polycythemia model]T Tassiopoulos, P Fessas, G Pangalis, et al.Cancer|May 1, 1977
Angio-immunoblastic lymphadenopathy terminating as Hodgkin's diseaseX Yataganas, C Papadimitriou, G Pangalis, et al.British Journal of Haematology|July 1, 1978
A unique thalassaemic syndrome: homozygous alpha-thalassaemia + homozygous beta-thalassaemiaD Loukopoulos, A Loutradi, P FessasAnnals of the New York Academy of Sciences|January 1, 1980
Proteolysis in thalassemia: studies with protease inhibitorsD Loukopoulos, A Karoulias, P FessasSchweizerische Medizinische Wochenschrift|October 8, 1983
Prevention of thalassemiaD Loukopoulos, A Kaltsoya-Tassiopoulou, P FessasBlood|April 1, 1980
Glycerol-3-phosphate dehydrogenase activity in the red cells of patients with thalassemiaP Fessas, N P Anagnou, D LoukopoulosHemoglobin|January 1, 1991
The origin of the sickle mutation in Greece; evidence from beta S globin gene cluster polymorphismsM Boussiou, D Loukopoulos, J Christakis, et al.British Journal of Haematology|August 1, 1982
'Silent' beta-thalassaemia caused by a 'silent' beta-chain mutant: the pathogenesis of a syndrome of thalassaemia intermediaP Fessas, D Loukopoulos, A Loutradi-Anagnostou, et al.American Journal of Hematology|February 1, 1986
Hemoglobin Knossos: a clinical, laboratory, and epidemiological studyP Fessas, D Loukopoulos, S Kokkinou, et al.Haematologia|January 1, 1995
Low incidence of acute myocardial infarction in beta-thalassaemia trait carriersT Tassiopoulos, G Stamatelos, N Zakopoulos, et al.Pageof 16