Results 31 to 40 of about 999,769 (295)

Promoter variants in tissue inhibitor of metalloproteinase-3 (TIMP-3) protect against susceptibility in pigeon breeders' disease. [PDF]

, 2004
BACKGROUND: Tissue inhibitors of metalloproteinases (TIMPs) play a major role in extracellular matrix turnover in the lung. However, in chronic lung disorders such as idiopathic pulmonary fibrosis (IPF) and pigeon breeders' disease (PBD), TIMPs may ...
Briggs, L, Montaño, MM, Pardo, A, Estrada, A, Laurent, GJ, Selman, M, Hill, MR, Pardo-Cemo, Annie   +7 more
core   +1 more source

Targeting PI3K/AKT signaling for treatment of idiopathic pulmonary fibrosis

Acta Pharmaceutica Sinica B, 2021
Idiopathic pulmonary fibrosis (IPF) is a chronic progressive fibrotic interstitial pneumonia with unknown causes. The incidence rate increases year by year and the prognosis is poor without cure.
Jin-Cheng Wang, Kai-Li Hu, Xuanyan Cai, Bo Yang, Qiao-Jun He, Jia-Jia Wang, Qin-Jie Weng   +6 more
semanticscholar   +1 more source

Mechanochemical alterations in lung cells during fibrogenesis [PDF]

, 2009
Màster en BiofísicaIdiopath pulmonary fibrosis (IPF) is a usually fatal disease associated with hardening of the lung tissue, epithelial injury and abnormal wound healing.
Pavelescu, Irina
core   +6 more sources

A sigmoidal fit for pressure-volume curves of idiopathic pulmonary fibrosis patients on mechanical ventilation: clinical implications

Clinics, 2011
OBJECTIVE: Respiratory pressure-volume curves fitted to exponential equations have been used to assess disease severity and prognosis in spontaneously breathing patients with idiopathic pulmonary fibrosis.
Juliana C. Ferreira, Fabio E. M. Benseñor, Marcelo J. J. Rocha, Joao M. Salge, R. Scott Harris, Atul Malhotra, Ronaldo A. Kairalla, Robert M. Kacmarek, Carlos R. R. Carvalho   +8 more
doaj   +1 more source

Idiopathic Pulmonary Fibrosis.

Presse medicale, 2023
Idiopathic pulmonary fibrosis (IPF) is a progressive devastating lung disease with substantial morbidity. It is associated with cough, dyspnea and impaired quality of life. If left untreated, IPF has a median survival of 3 years.
T. Koudstaal, M. Wijsenbeek
semanticscholar   +1 more source

Acute worsening of native lung fibrosis after single lung transplantation for pulmonary fibrosis: two case reports

Journal of Medical Case Reports, 2022
Background In patients receiving single lung transplantation for idiopathic pulmonary fibrosis, worsening of fibrosis of the native lung is usually progressive over time, with no significant effects on gas exchange.
Tiphaine Goletto, Sixtine Decaux, Vincent Bunel, Gaëlle Weisenburger, Jonathan Messika, Samer Najem, Chahine Medraoui, Cendrine Godet, Marie Pierre Debray, Brice Lortat-Jacob, Pierre Mordant, Yves Castier, Lila Bouadma, Raphael Borie, Hervé Mal   +14 more
doaj   +1 more source

IDIOPATHIC PULMONARY FIBROSIS. CORRECTION OF ERRORS

Вестник рентгенологии и радиологии, 2018
Substantial changes have been recently made in the concept of the diagnosis of idiopathic pulmonary fibrosis. The concept of disease pathogenesis and the pathomorphologic criteria for diagnosing usual interstitial pneumonia have been revised.
A. L. Yudin, Yu. A. Abovich, N. I. Afanas’eva   +2 more
doaj   +1 more source

Efficacy of Pirfenidone and Nintedanib in Interstitial Lung Diseases Other than Idiopathic Pulmonary Fibrosis: A Systematic Review

International Journal of Molecular Sciences, 2023
Pirfenidone and nintedanib are antifibrotic medications approved for idiopathic pulmonary fibrosis treatment by regulatory agencies and available for clinical use worldwide.
F. Amati, A. Stainer, Veronica Polelli, M. Mantero, A. Gramegna, Francesco Blasi, S. Aliberti   +6 more
semanticscholar   +1 more source

Rare and common variants in KIF15 contribute to genetic risk of idiopathic pulmonary fibrosis [PDF]

, 2022
RATIONALE: Genetic studies of Idiopathic Pulmonary Fibrosis (IPF) have improved our understanding of this disease, but not all causal loci have been identified.
Newton, Chad A, Povysil, Gundula, Martinez, Fernando J, Garcia, Joseph A, Petrovski, Slavé, Li, Qi, Maher, Toby M, Garcia, Christine Kim, Kobeissy, Philippe H, Raghu, Ganesh, Amelotte, Mason, Goldstein, David B, Haefliger, Carolina, Wang, Binhan, Molyneaux, Philip L, Jaouadi, Hager, Noth, Imre, Todd, Jamie L, Palmer, Scott M, Platt, Adam, Zhang, David   +20 more
core   +1 more source

Idiopathic pulmonary fibrosis: evaluation of progression and prognosis after the ATS/ERS/JRS/ALAT statement 2011 [PDF]

, 2012
Objectives The prediction of usual interstitial pneumonia (UIP) progression and prognosis by the a application of HRCT criteria pattern recommended by ATS/ERS/JALAT guidelines 2011 Materials and methods Two radiologists after assessing the baseline HRCT ...
ROMEI, CHIARA
core   +1 more source