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Long-term experience in the treatment of α(1)-antitrypsin deficiency: 25 years of augmentation therapy

Although it is often under-recognised, α(1)-antitrypsin deficiency (AATD) represents one of the most common genetic respiratory disorders worldwide. Since the publication of studies in the late 1980s, which demonstrated that plasma-derived augmentation therapy with intravenous α(1)-antitrypsin (AAT)...

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Detalles Bibliográficos
Autor principal: Teschler, Helmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9487776/
https://www.ncbi.nlm.nih.gov/pubmed/25726554
http://dx.doi.org/10.1183/09059180.10010714