Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study

BACKGROUND: Registration of trigger factors, prodromal symptoms, swelling localization, therapeutic behavior and gender-specific differences of the largest cohort of patients with hereditary angioedema due to C1-Inhibitor deficiency (C1-INH-HAE) in Switzerland. METHODS: Questionnaire survey within a...

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Publicado en:Orphanet J Rare Dis
Autores principales: Steiner, Urs C., Weber-Chrysochoou, Christina, Helbling, Arthur, Scherer, Kathrin, Grendelmeier, Peter Schmid, Wuillemin, Walter A.
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4839073/
https://ncbi.nlm.nih.gov/pubmed/27101900
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0423-1
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