Results 41 to 50 of about 28,410 (256)

Development of a Consensus Statement for the Definition, Diagnosis, and Treatment of Acute Exacerbations of Idiopathic Pulmonary Fibrosis Using the Delphi Technique. [PDF]

, 2015
© 2015, The Author(s).Introduction: There is a lack of agreed and established guidelines for the treatment of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF).
Bennett, BM, Hoyles, RK, Maher, TM, Mathieson, N, Ochiai, Y, Parfrey, H, Turnbull, A, Whyte, MK, Williamson, N   +8 more
core   +2 more sources

State of the Art in Idiopathic Pulmonary Fibrosis

Cells, 2022
Idiopathic pulmonary fibrosis (IPF) is a form of usual interstitial pneumonia (UIP), though its origin is unknown [...]
Elie El Agha, Malgorzata Wygrecka
doaj   +1 more source

Increased expression of 5-hydroxytryptamine(2A/B) receptors in idiopathic pulmonary fibrosis: a rationale for therapeutic intervention [PDF]

, 2010
Background Idiopathic pulmonary fibrosis (IPF) has a poor prognosis and limited responsiveness to available treatments. It is characterised by epithelial cell injury, fibroblast activation and proliferation and extracellular matrix deposition ...
Amarie, Oana Veronica, Dumitrascu, Rio, Eickelberg, Oliver, Grimminger, Friedrich, Königshoff, Melanie, Reiter, Rudolf, Schermuly, Ralph Theo, Seeger, Werner, Udalov, Sergey   +8 more
core   +1 more source

Clinical Course of Usual Interstitial Pneumonia [PDF]

Tuberculosis and Respiratory Diseases, 2000
Background : Idiopathic pulmonary fibrosis (IPF) is a fatal progressive fibrous disease of the lung of unknown etiology. Recently it has been classified into several distinct entities on the basis of pathologic and clinical characteristics, ie : usual interstitial pneumonia (UIP), desquamative interstitial pneumonia (DIP), acute interstitial pneumonia (
Woo Sung Kim, Younsuck Koh, Tae Sun Shim, Chae Man Lim, Sang Do Lee, Dong Soon Kim, Joo Hun Park, Masanori Kitaichi, Won Dong Kim, Ho Kee Yum   +9 more
openaire   +1 more source

Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood [PDF]

, 2018
Background: Hermansky-Pudlak syndrome (HPS), a hereditary multisystem disorder with oculocutaneous albinism, may be caused by mutations in one of at least 10 separate genes.
Brasch, F. (Frank), Griese, M. (Matthias), Grosse-Onnebrink, J. (Joerg), Guenther, A. (Andreas), Hengst, M. (Meike), Ley-Zaporozhan, J. (Julia), Mahavadi, P. (Poornima), Naehrlich, L. (Lutz), Reu, S. (Simone), Schuch, L.A. (Luise A.), Skanke, L.Hø. (Lars Høsøien), Terheggen-Lagro, S. (Suzanne)   +11 more
core   +2 more sources

Idiopathic Interstitial Pneumonias and COVID-19 Pneumonia: Review of the Main Radiological Features and Differential Diagnosis

Tomography, 2021
COVID-19 pneumonia represents a challenging health emergency, due to the disproportion between the high transmissibility, morbidity, and mortality of the virus and healthcare systems possibilities.
Alessia Guarnera, Elena Santini, Pierfrancesco Podda   +2 more
doaj   +1 more source

Histological features and survival in idiopathic pulmonary fibrosis [PDF]

, 2003
BACKGROUND: Idiopathic pulmonary fibrosis was recently redefined as usual interstitial pneumonia of unknown etiology. Consequently, the prognostic value of histological findings needs to be reassessed.
Coletta, Ester Nei Aparecida Martins, Ferreira, Rimarcs Gomes, Nunes, Tatiana Santos Malheiros, Pereira, Carlos Alberto de Castro, Rubin, Adalberto Sperb, Stávale, João Norberto, Villela, Lucimara Sonja   +6 more
core   +2 more sources

Video-Assisted Thoracoscopic Lung Biopsy as a Possible Cause of Acute Interstitial Pneumonia in a Patient with Nonspecific Interstitial Pneumonia

Canadian Respiratory Journal, 2004
The present case report describes a 44-year-old woman who presented with dyspnea due to diffuse interstitial lung disease. High-resolution computed tomography showed features of usual interstitial pneumonia, but the lung biopsy obtained by video-assisted
D Jeffrey Moore, Colm P McParland, Martin J Bullock, Yannick Cartier, Paul Hernandez   +4 more
doaj   +1 more source

Comorbid Conditions in Idiopathic Pulmonary Fibrosis: Recognition and Management. [PDF]

, 2017
Idiopathic pulmonary fibrosis (IPF), a fibrosing interstitial pneumonia of unknown etiology, primarily affects older adults and leads to a progressive decline in lung function and quality of life.
Collard, Harold R, Oldham, Justin M
core   +2 more sources

Evaluation of the histological parameters in usual interstitial pneumonia (idiopathic pulmonary fibrosis) [PDF]

, 2000
Idiopathic pulmonary fibrosis (cryptogenic fibrosing alveolitis) is a progressive interstitial pulmonary disease of unknown etiology. Since Hamman's and Rich's (1944) reports, many studies have tried to find a histological marker for the correlation ...
Coletta, Ester Nei Aparecida Martins, Ferreira, Rimarcs Gomes, Giannotti Filho, Osvaldo   +2 more
core   +3 more sources