Πλοήγηση ανά Συγγραφέα "Papadopoulou-Alataki, E."
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Hereditary angioedema in Greek families caused by novel and recurrent mutations
Speletas, M.; Boukas, K.; Papadopoulou-Alataki, E.; Tsitsami, E.; Germenis, A. E. (2009)This study constitutes the first molecular analysis of hereditary angioedema (HAE) in Greece, where 11 patients from three unrelated families with recurrent angioedema attacks and decreased C1 inhibitor antigenic levels ... -
Influence of mannose-binding lectin (MBL) deficiency on the clinical presentation of patients with antibody deficiencies
Speletas, M.; Iordanakis, G.; Mamara, A.; Florou, Z.; Papadopoulou-Alataki, E.; Germenis, A. E. (2012) -
SIALIC ACID ACETYLESTERASE (SIAE) MUTATIONS ARE NOT ASSOCIATED WITH AUTOIMMUNE DISEASE RISK IN PATIENTS WITH ANTIBODY DEFICIENCIES
Speletas, M.; Sevdali, E.; Zisimatos, A.; Papadopoulou-Alataki, E.; Germenis, A. E. (2012) -
TNFRSF13B/TACI Alterations in Greek Patients with Antibody Deficiencies
Speletas, M.; Mamara, A.; Papadopoulou-Alataki, E.; Iordanakis, G.; Liadaki, K.; Bardaka, F.; Kanariou, M.; Germenis, A. E. (2011)TNFRSF13B/TACI defects have recently been associated with common variable immunodeficiency (CVID) pathogenesis. Considering that TNFRSF13B/TACI is very polymorphic and the frequency of its alterations may be different in ...