Serum surfactant proteins A and D as prognostic factors in idiopathic pulmonary fibrosis and their relationship to disease extent

Idiopathic pulmonary fibrosis (IPF) is a progressive, life-threatening, interstitial lung disease of unknown etiology. For optimal therapeutic management of IPF an accurate tool is required for discrimination between reversible and irreversible types of the disease. However, such noninvasive tools a...

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Veröffentlicht in:	American journal of respiratory and critical care medicine 2000-09, Vol.162 (3), p.1109-1114
Hauptverfasser:	TAKAHASHI, Hiroki, FUJISHIMA, Takuya, KOBA, Hiroyuki, MURAKAMI, Seiji, KUROKAWA, Keizo, SHIBUYA, Yoshie, SHIRATORI, Masanori, KUROKI, Yoshio, ABE, Shosaku
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Biological and medical sciences Disease Progression Female Humans Male Medical sciences Middle Aged Pneumology Prognosis Proteolipids - blood Pulmonary Fibrosis - blood Pulmonary Fibrosis - diagnosis Pulmonary Fibrosis - mortality Pulmonary Surfactant-Associated Protein A Pulmonary Surfactant-Associated Proteins Pulmonary Surfactants - blood Reference Values Respiratory system : syndromes and miscellaneous diseases Smoking - adverse effects Survival Rate
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