Autoantibodies to multiple cytokines have been identified and some, including antibodies
against granulocyte-macrophage colony-stimulating factor (GM-CSF), have been associated …

Pulmonary alveolar proteinosis (PAP) is a rare, diffuse lung disease characterized by
accumulation of lipoprotein in lung surfactant in the alveolar space and terminal bronchioles …

Pulmonary alveolar proteinosis (PAP) is a rare lung disease where there is accumulation of
surfactant in the alveoli. It can be classified based on the underlying aetiology into three …

Abstract A 67-year-old male, with a history of severe COVID-19 infection and exposure to
talc was seen for worsening shortness of breath for months, requiring supplemental oxygen …

Acute respiratory distress syndrome (ARDS) is a serious pulmonary reaction with well-
defined clinical parameters in humans triggered by many causes besides bacterial and viral …

Autoimmune pulmonary alveolar proteinosis (APAP) is caused by macrophage dysfunction
owing to the presence of anti-granulocyte-macrophage colony-stimulating factor (GM-CSF) …

Los autoanticuerpos anticitocinas (ACAA) han sido reportados como causa importante de
inmunodeficiencias secundarias. Altos títulos de autoanticuerpos neutralizantes pueden …

Resumen CORTES-ACEVEDO, Paulina; MENDOZA-ELVIRA, Susana E.; DOFFINGER,
Rainer y BARCENAS-MORALES, Gabriela. Secondary immunodeficiencies related to the …

La proteinosis alveolar pulmonar es una enfermedad difusa que se debe a la acumulación
de surfactante en los alveolos y que puede causar disnea y de manera progresiva llegar a …

Proteinosis alveolar pulmonar y lesión pulmonar inducida por uso de cigarrillo o vapeador
electrónico (EVALI) Page 1 ISSN 2072-8174 versión impresa Rev. Nac. (Itauguá). 2023;15(1):059-067 …