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Hereditary angioedema C1-esterase inhibitor replacement therapy and coexisting autoimmune disorders: findings from a claims database

In this letter to the editor, we present results of claims data analysis. This claims data analysis supports a hypothesis that in patients with hereditary angioedema due to C1-esterase inhibitor (C1-INH) deficiency, the occurrence and/or symptomatology of coexisting autoimmune disease may be positiv...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Allergy Asthma Clin Immunol
Prif Awduron: Farkas, Henriette, Levy, Donald, Supina, Dylan, Berger, Melvin, Prusty, Subhransu, Fridman, Moshe
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2020
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7254637/
https://ncbi.nlm.nih.gov/pubmed/32514273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13223-020-00439-9
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