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Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a type of chronic scarring lung disease characterized by a progressive and irreversible decline in lung function
Pulmonary fibrosis
suppressive treatment probably do not have idiopathic pulmonary fibrosis, for idiopathic pulmonary fibrosis has no significant treatment or cure. Two pharmacological
Interstitial lung disease
chILD. Prolonged ILD may result in pulmonary fibrosis, but this is not always the case. Idiopathic pulmonary fibrosis is interstitial lung disease for which
Fibrosis
examples include: Lungs Pulmonary fibrosis Cystic fibrosis Idiopathic pulmonary fibrosis (idiopathic meaning the cause is unknown) Radiation-induced lung
Idiopathic pulmonary haemosiderosis
Idiopathic pulmonary haemosiderosis (IPH) is a lung disease of unknown cause that is characterized by alveolar capillary bleeding and accumulation of haemosiderin
Nintedanib
and Vargatef, is an oral medication used for the treatment of idiopathic pulmonary fibrosis and along with other medications for some types of non-small-cell
Pirfenidone
is a medication used for the treatment of idiopathic pulmonary fibrosis. It works by reducing lung fibrosis through downregulation of the production of
Restrictive lung disease
disease are idiopathic (have no known cause). Still, there is generally pulmonary fibrosis. Examples are: Idiopathic pulmonary fibrosis Idiopathic interstitial
Usual interstitial pneumonia
conditions of unknown cause is "idiopathic", the clinical term for UIP of unknown cause is idiopathic pulmonary fibrosis (IPF). Examples of known causes
Idiopathic interstitial pneumonia
200602-019TK. PMID 16738196. Katzenstein AL, Myers JL (1998). "Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification". Am. J. Respir