Listar por autor "Koutsostathis, N."
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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema
Speletas, M.; Szilágyi, Á; Csuka, D.; Koutsostathis, N.; Psarros, F.; Moldovan, D.; Magerl, M.; Kompoti, M.; Varga, L.; Maurer, M.; Farkas, H.; Germenis, A. E. (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
Psarros, F.; Koutsostathis, N.; Farmaki, E.; Speletas, M. G.; Germenis, A. E. (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 ...