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pro vyhledávání: '"Elisabeth M. Bendstrup"'
Publikováno v:
Respiratory Medicine Case Reports, Vol 23, Iss , Pp 167-169 (2018)
Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare parenchymal lung disease characterized by accumulation of surfactant in the airways with high levels of granulocyte-macrophage colony stimulating factor (GM-CSF) antibodies in blood. Disease
Externí odkaz:
https://doaj.org/article/ad655950708a404a96e123cd77088d3c
