Zobrazeno 1 - 3
of 3
pro vyhledávání: '"functional polymorphism KLKB1-428G/A"'
Введение. Врожденный ангионевротический отек (ВАО) – редкое генетическое заболевание с аутосомно-доминантным типом наследования, хара
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8439d86434bf53508998718a902f25ea
Autor:
Gianni, Panagiota, Loules, Gedeon, Zamanakou, Maria, Kompoti, Maria, Csuka, Dorottya, Psarros, Fotis, Magerl, Markus, Moldovan, Dimitru, Maurer, Marcus, Speletas, Matthaios G., Farkas, Henriette, Germenis, anastasios E.
Publikováno v:
International Archives of Allergy & Immunology; Dec2017, Vol. 174 Issue 3/4, p200-204, 5p
Autor:
Henriette Farkas, Dorottya Csuka, Anastasios E. Germenis, Fotis Psarros, Markus Magerl, Gedeon Loules, Marcus Maurer, Maria Zamanakou, Matthaios Speletas, Panagiota Gianni, Maria Kompoti, Dimitru Moldovan
Publikováno v:
International Archives of Allergy and Immunology. 174:200-204
Background: In view of the large heterogeneity in the clinical presentation of hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE), great efforts are being made towards detecting measurable biological determinants of disease severity th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0b6eaa8e4f3bade0e896030fa20392f
https://doi.org/10.1159/000481987
https://doi.org/10.1159/000481987