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549 Management of Twenty-Five Pediatric Patients with Hereditary Angioedema (Hae) Undergoing Home Treatment—A Clinical Surveillance Program

BACKGROUND: Hereditary angioedema (HAE) is a rare disorder characterized by C1 esterase inhibitor (C1-INH) deficiency. Clinically, HAE is characterized by relapsing episodes of edema at various body sites followed by disease-free intervals of variable duration. Episodes of upper airway obstruction (...

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Detalhes bibliográficos
Main Authors: Martinez-Saguer, Inmaculada, Aygören-Pürsün, Emel, Rusicke, Eva, Klingebiel, Thomas, Kreuz, Wolfhart
Formato: Artigo
Idioma:Inglês
Publicado em: World Allergy Organization Journal 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3512583/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.WOX.0000411664.07634.b7
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