Results 291 to 300 of about 117,210 (347)

The distribution and the clinical importance of MUC5B and TERT variants in Turkish patients with idiopathic pulmonary fibrosis. [PDF]

BMC Pulm Med
Ödemiş A, Öğüş AC, Toylu A, Dirol H, Çilli A, Özbudak Ö, Altıok Clark Ö, Özdemir T.   +7 more
europepmc   +1 more source

Quality of life in patients with hypersensitivity pneumonitis and with idiopathic pulmonary fibrosis in real-life clinical practice. [PDF]

J Thorac Dis
Suvorova OA, Trushenko NV, Lavginova BB, Levina IA, Chikina SY, Merzhoeva ZM, Nekludova GV, Avdeev SN.   +7 more
europepmc   +1 more source

Cardiovascular disease in idiopathic pulmonary fibrosis: a systematic review and meta-analysis of observational studies. [PDF]

Front Med (Lausanne)
Li Y, Tan W, Zhang Y, Cao F, Wu Z, Jiao Y, Niu J.   +6 more
europepmc   +1 more source

Genome-wide analysis of tandem repeat variation identifies SLC15A4 as a susceptibility gene for idiopathic pulmonary fibrosis

Oketch JW, Albahimah A, Barca A, Allen R, Shrine N, Walewski B, Sidekli O, Alyassi A, Romano A, Jenkins RG, Maher TM, Molyneaux PL, Stewart I, Verri T, Wain LV, Hollox EJ.   +15 more
europepmc   +1 more source

Masthead: (View 6/2025)

VIEW, Volume 6, Issue 6, December 2025.
wiley   +1 more source

Polygenic Risk and Rare Variants in Endotypes of Idiopathic Pulmonary Fibrosis

Duckworth A, Jackson L, Green H, Khan A, Wang C, Condescu A, Hawkes G, Noth I, Martinez FJ, Raghu G, Newton CA, Moll M, Cho M, Gibbons M, Scotton CJ, Columbia Genomics Consortium, Kiryluk K, Garcia CK, Zhang D.   +18 more
europepmc   +1 more source

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Idiopathic Pulmonary Fibrosis

Seminars in Respiratory and Critical Care Medicine, 2012
Idiopathic pulmonary fibrosis (IPF) is a specific form of progressive, chronic fibrosing interstitial lung disease occurring primarily in older adults and limited to the lungs. The prognosis is dire, with half of all patients progressing to death from respiratory failure within 3 to 5 years from initial diagnosis. The pathogenesis of IPF is complex and
Jessica M, Adkins, Harold R, Collard
openaire   +4 more sources

Idiopathic Pulmonary Fibrosis and Progressive Pulmonary Fibrosis

Immunology and Allergy Clinics of North America, 2023
Idiopathic pulmonary fibrosis (IPF), a common interstitial lung disease (ILD), is a chronic, progressive fibrosing interstitial pneumonia, with an unknown cause. IPF has been linked to several genetic and environmental risk factors. Disease progression is common and associated with worse outcomes.
Rachel, Strykowski, Ayodeji, Adegunsoye
openaire   +2 more sources