Parcourir par auteur "Magerl M., Germenis A.E., Maas C., Maurer M."
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Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment
Magerl M., Germenis A.E., Maas C., Maurer M. (2017)A new form of hereditary angioedema (HAE) was identified in the year 2000. Its clinical appearance resembles HAE types I and II, which are caused by mutations that result in a deficiency of C1 inhibitor (C1-INH). In patients ...