Φορτώνει......
Self-administered C1 esterase inhibitor concentrates for the management of hereditary angioedema: usability and patient acceptance
Hereditary angioedema (HAE) is a rare genetic disease characterized by episodic subcutaneous or submucosal swelling. The primary cause for the most common form of HAE is a deficiency in functional C1 esterase inhibitor (C1-INH). The swelling caused by HAE can be painful, disfiguring, and life-threat...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Patient Prefer Adherence |
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| Κύριος συγγραφέας: | |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Dove Medical Press
2016
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5019432/ https://ncbi.nlm.nih.gov/pubmed/27660422 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PPA.S86379 |
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