Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nirelcio, Galao"'
Publikováno v:
Allergologia et Immunopathologia. 49:1-3
Hereditary angioedema (HAE) is an autosomal dominant disease, characterized by edema attacks resulting from quantitative and/or functional deficiency of the C1 inhibitor (C1-INH), which acts in controlling the complement, coagulation, fibrinolysis, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0c30439bbe68fa0037fba6d5945fc94
https://doi.org/10.15586/aei.v49i4.57
https://doi.org/10.15586/aei.v49i4.57
Publikováno v:
Allergologia et immunopathologia. 49(4)
Hereditary angioedema (HAE) is an autosomal dominant disease, characterized by edema attacks resulting from quantitative and/or functional deficiency of the C1 inhibitor (C1-INH), which acts in controlling the complement, coagulation, fibrinolysis, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5674c07a1e78ef9c1c6037ae59be813c
https://pubmed.ncbi.nlm.nih.gov/34224212
https://pubmed.ncbi.nlm.nih.gov/34224212