sábado, 29 de agosto de 2020

A Germany-wide survey study on the patient journey of patients with hereditary angioedema | Orphanet Journal of Rare Diseases | Full Text

A Germany-wide survey study on the patient journey of patients with hereditary angioedema | Orphanet Journal of Rare Diseases | Full Text

Hereditary angioedema (HAE) is a rare genetic disease and characterized by clinical features such as paroxysmal, recurrent angioedema of the skin, the gastrointestinal tract, and the upper airways. Swelling of...
Authors:Markus Magerl, Holger Gothe, Simon Krupka, Anja Lachmann and Christoph Ohlmeier
Citation:Orphanet Journal of Rare Diseases 2020 15:221
Content type:Research
 
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