Cargando…
The establishment and utility of Sweha-Reg: a Swedish population-based registry to understand hereditary angioedema
BACKGROUND: The importance of acquiring comprehensive epidemiological and clinical data on hereditary angioedema has increasingly caught the attention of physicians and scientists around the world. The development of networks and creation of comprehensive policies to improve care of people suffering...
Autores principales: | Mallbris, Lotus, Nordenfelt, Patrik, Björkander, Janne, Lindfors, Anders, Werner, Sonja, Wahlgren, Carl-Fredrik |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151953/ https://www.ncbi.nlm.nih.gov/pubmed/18053127 http://dx.doi.org/10.1186/1471-5945-7-6 |
Ejemplares similares
-
Comorbidities in hereditary angioedema—A population‐based cohort study
por: Sundler Björkman, Linda, et al.
Publicado: (2022) -
Hereditary angioedema
por: Lesser, Helen, et al.
Publicado: (2021) -
Hereditary Angioedema
por: Banerjee, Anjali, et al.
Publicado: (2023) -
2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema
por: Bowen, Tom, et al.
Publicado: (2010) -
The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency
por: Zanichelli, Andrea, et al.
Publicado: (2021)