Cargando…
Clinical Characteristics and Management of Angioedema Attacks in Polish Adult Patients with Hereditary Angioedema Due to C1-Inhibitor Deficiency
Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency is a rare disease characterized by recurrent swellings. This study aims to determine (i) the clinical characteristics of the HAE patient population from Poland, and (ii) real-life patients’ treatment practices. A cross-sectional stu...
Autores principales: | Piotrowicz-Wójcik, Katarzyna, Bulanda, Małgorzata, Juchacz, Aldona, Jamróz-Brzeska, Joanna, Gocki, Jacek, Kuziemski, Krzysztof, Pawłowicz, Robert, Porebski, Grzegorz |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658320/ https://www.ncbi.nlm.nih.gov/pubmed/34884311 http://dx.doi.org/10.3390/jcm10235609 |
Ejemplares similares
-
Biomarkers in Hereditary Angioedema
por: Porebski, Grzegorz, et al.
Publicado: (2021) -
Genetic variants of SERPING1 gene in Polish patients with hereditary angioedema due to C1 inhibitor deficiency
por: OBTULOWICZ, KRYSTYNA, et al.
Publicado: (2020) -
Abdominal and pelvic imaging in the diagnosis of acute abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency
por: Obtułowicz, Piotr, et al.
Publicado: (2021) -
Food as a trigger for abdominal angioedema attacks in patients with hereditary angioedema
por: Steiner, Urs C., et al.
Publicado: (2018) -
Advances in Hereditary Angioedema: The Prevention of Angioedema Attacks With Subcutaneous C1-Inhibitor Replacement Therapy
por: Lumry, William, et al.
Publicado: (2020)