Cardiovascular risk in patients with alpha-1-antitrypsin deficiency

BACKGROUND: Alpha-1-antitrypsin deficiency (AATD) is a rare inherited condition caused by mutations of the SERPINA1 gene that is associated with the development of a COPD like lung disease. The comorbidities in patients with AATD-related lung diseases are not well defined. The aim of this study was...

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Detalles Bibliográficos
Autores principales: Fähndrich, Sebastian, Biertz, Frank, Karch, Annika, Kleibrink, Björn, Koch, Armin, Teschler, Helmut, Welte, Tobias, Kauczor, Hans-Ulrich, Janciauskiene, Sabina, Jörres, Rudolf A., Greulich, Timm, Vogelmeier, Claus F., Bals, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602961/
https://www.ncbi.nlm.nih.gov/pubmed/28915894
http://dx.doi.org/10.1186/s12931-017-0655-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602961/
https://www.ncbi.nlm.nih.gov/pubmed/28915894
http://dx.doi.org/10.1186/s12931-017-0655-1

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