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Disease burden associated with alpha-1 antitrypsin deficiency: systematic and structured literature reviews
Alpha-1 antitrypsin deficiency (AATD) is a rare genetic disorder characterised by reduced levels of circulating alpha-1 antitrypsin and an increased risk of lung and liver disease. Recent reviews of AATD have focused on diagnosis, epidemiology and clinical management; comprehensive reviews examining...
Autores principales: | Miravitlles, Marc, Herepath, Mike, Priyendu, Asim, Sharma, Sheetal, Vilchez, Tatiana, Vit, Oliver, Haensel, Michaela, Lepage, Virginie, Gens, Helena, Greulich, Timm |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488933/ https://www.ncbi.nlm.nih.gov/pubmed/35321931 http://dx.doi.org/10.1183/16000617.0262-2021 |
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