Inflammatory markers in chronic obstructive pulmonary disease patients with different α1 antitrypsin genotypes

INTRODUCTION: Chronic obstructive pulmonary disease (COPD) has been recently defined as a systemic pulmonary inflammatory disease, and congenital α1 antitrypsin deficiency is one of the well-established genetic risk factors for chronic obstructive pulmonary disease. The aim of our study was to evalu...

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Detalles Bibliográficos
Autores principales: Serapinas, Danielius, Sitkauskiene, Brigita, Sakalauskas, Raimundas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2012
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542496/
https://www.ncbi.nlm.nih.gov/pubmed/23319981
http://dx.doi.org/10.5114/aoms.2012.32414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542496/
https://www.ncbi.nlm.nih.gov/pubmed/23319981
http://dx.doi.org/10.5114/aoms.2012.32414

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