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Glycosaminoglycans and glycoproteins in bronchoalveolar lavage fluid from patients with pulmonary alveolar proteinosis

โœ Scribed by Ken Satoh; Hideo Arai; Tsukasa Yoshida; Masayuki Ito; Hiromi Nagai; Hirosi Sato; Masakichi Motomiya; Kiyoshi Konno


Publisher
Springer
Year
1983
Tongue
English
Weight
417 KB
Volume
7
Category
Article
ISSN
0360-3997

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Pulmonary alveolar proteinosis with myel
โœ Seth M. Pollack; Guillermo Gutierrez; Joao Ascensao ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 208 KB ๐Ÿ‘ 1 views

Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by surfactant component accumulation in the alveolar space. Primary PAP is likely an autoimmune disorder caused by antibodies to granulocyte-macrophage colony stimulating factor (GM-CSF). When an underlying disease causes PAP, thi