Canadian Respiratory Journal, 2004 The case of a patient that developed pulmonary fibrosis two months after initiation of danazol for treatment of idiopathic thrombocytopenic purpura is described.
Smita Pakhale +3 more
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The pulmonary vasculature in lethal COVID-19 and idiopathic pulmonary fibrosis at single-cell resolution [PDF]
, 2022 Laura de Rooij +47 more
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Idiopathic Pulmonary Fibrosis and Lung Cancer: Mechanisms and Molecular Targets
International Journal of Molecular Sciences, 2019 Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pulmonary disease with a median survival of 2–4 years after diagnosis.
Beatriz Ballester, J. Milara, J. Cortijo
semanticscholar +1 more source
LONG TERM EXPERIENCE WITH BOSENTAN IN PATIENTS WITH PULMONARY ARTERIAL HYPERTENSION (PAH) ASSOCIATED WITH ADVANCED IDIOPATHIC PULMONARY FIBROSIS (IPF) AND INTERSTITIAL LUNG DISEASE (ILD): A RETROSPECTIVE CASE SERIES [PDF]
, 2005 Ganesh Raghu +4 more
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Familial idiopathic pulmonary fibrosis in a young female
Respiratory Medicine Case Reports, 2018 Idiopathic pulmonary fibrosis is a chronic interstitial lung disease of unknown cause. In the past years there have been observations of clustering of pulmonary fibrosis in families, indicating the disease can be inherited.
Sajitha S. Sritharan +4 more
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P9 Cough Is Prevalent In Higher Proportion Of Older Patients With Both Idiopathic Pulmonary Fibrosis And Non-specific Interstitial Lung Disease [PDF]
, 2014 G. Saini +7 more
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Modeling Progressive Fibrosis with Pluripotent Stem Cells Identifies an Anti-fibrotic Small Molecule. [PDF]
, 2019 Progressive organ fibrosis accounts for one-third of all deaths worldwide, yet preclinical models that mimic the complex, progressive nature of the disease are lacking, and hence, there are no curative therapies. Progressive fibrosis across organs shares
Ahadome, Sarah D +21 more
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High serum concentrations of autoantibodies to HSP47 in nonspecific interstitial pneumonia compared with idiopathic pulmonary fibrosis [PDF]
, 2008 Tomoyuki Kakugawa +10 more
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Dyskeratosis Congenita Associated Non-Specific Interstitial Pneumonia [PDF]
Journal of Krishna Institute of Medical Sciences University, 2017 Dyskeratosis Congenita (DC) is a rare inherited disorder of ectodermal dysplasia. It consists of a classical mucocutaneous triad of abnormal skin pigmentation, nail dystrophy and leukoplakia. Pulmonary disease is seen in 10-15%.
Unnati D. Desai , Jyotsna M. Joshi
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