Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12325-022-02401-0.pdf
Reference64 articles.
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2. Andrejević S, Korošec P, Šilar M, Košnik M, Mijanović R, Bonači-Nikolić B, et al. Hereditary angioedema due to C1 inhibitor deficiency in Serbia: two novel mutations and evidence of genotype–phenotype association. PLoS ONE. 2015;10(11): e0142174.
3. Nasr IH, Manson AL, Al Wahshi HA, Longhurst HJ. Optimizing hereditary angioedema management through tailored treatment approaches. Expert Rev Clin Immunol. 2016;12(1):19–31.
4. Nordenfelt P, Nilsson M, Björkander JF, Mallbris L, Lindfors A, Wahlgren CF. Hereditary angioedema in Swedish adults: report from the national cohort. Acta Derm Venereol. 2016;96(4):540–5.
5. Patel G, Pongracic JA. Hereditary and acquired angioedema. Allergy Asthma Proc. 2019;40(6):441–5. https://doi.org/10.2500/aap.2019.40.4267. PMID: 31690390.
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