Πλοήγηση ανά Θέμα "Hereditary angioedema"
Αποτελέσματα 1-3 από 3
-
F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema
(2015)The factors influencing the heterogeneous clinical manifestation of hereditary angioedema due to C1-INH deficiency (C1-INH-HAE) represent one of the oldest unsolved problems of the disease. Considering that factor XII ... -
Hereditary Angioedema in Greece: The First Results of the Greek Hereditary Angioedema Registry
(2014)Background: No published data presently exist concerning hereditary angioedema (HAE) in Greece. The aim of this study was to present the results from patients recorded by the Greek Hereditary Angioedema Registry over the ... -
Hereditary angioedema in Greek families caused by novel and recurrent mutations
(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 ...