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Quoted phrase not found in phrase index: "Surfactant metabolism dysfunction, pulmonary, 5"
Page 1
Higher versus lower positive end-expiratory pressures in patients with the acute respiratory distress syndrome.
Brower RG, Lanken PN, MacIntyre N, Matthay MA, Morris A, Ancukiewicz M, Schoenfeld D, Thompson BT; National Heart, Lung, and Blood Institute ARDS Clinical Trials Network. Brower RG, et al. N Engl J Med. 2004 Jul 22;351(4):327-36. doi: 10.1056/NEJMoa032193. N Engl J Med. 2004. PMID: 15269312 Free article. Clinical Trial.
Higher PEEP levels may improve oxygenation and reduce ventilator-induced lung injury but may also cause circulatory depression and lung injury from overdistention. ...CONCLUSIONS: These results suggest that in patients with acute lung injury and ARDS who rece …
Higher PEEP levels may improve oxygenation and reduce ventilator-induced lung injury but may also cause circulatory depression and …
Pulmonary alveolar proteinosis.
Wang T, Lazar CA, Fishbein MC, Lynch JP 3rd. Wang T, et al. Semin Respir Crit Care Med. 2012 Oct;33(5):498-508. doi: 10.1055/s-0032-1325160. Epub 2012 Sep 21. Semin Respir Crit Care Med. 2012. PMID: 23001804
Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by the accumulation of surfactant lipids and protein in the alveolar spaces, with resultant impairment in gas exchange. ...Inherited or congenital forms of PAP are exceptionally rare and caused by
Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by the accumulation of surfactant lipids and protein in
Early life surfactant protein-D levels in bronchoalveolar lavage fluids of extremely preterm neonates.
De Luca D, Arroyo R, Foligno S, Autilio C, Touqui L, Kingma PS. De Luca D, et al. Am J Physiol Lung Cell Mol Physiol. 2023 Oct 1;325(4):L411-L418. doi: 10.1152/ajplung.00079.2023. Epub 2023 Jul 25. Am J Physiol Lung Cell Mol Physiol. 2023. PMID: 37489844
Surfactant protein-D (SP-D) is a hydrophilic protein with multiple crucial anti-inflammatory and immunological functions. It might play a role in the development and course of pulmonary infections, acute respiratory distress syndrome, and other respiratory di
Surfactant protein-D (SP-D) is a hydrophilic protein with multiple crucial anti-inflammatory and immunological functions. It might pl
ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system.
Peca D, Cutrera R, Masotti A, Boldrini R, Danhaive O. Peca D, et al. Biochem Soc Trans. 2015 Oct;43(5):913-9. doi: 10.1042/BST20150100. Biochem Soc Trans. 2015. PMID: 26517903 Free article. Review.
ABCA3 [ATP-binding cassette (ABC), subfamily A, member 3] is a lung-specific phospholipid transporter critical for intracellular surfactant synthesis and storage in lamellar bodies (LBs). ...Bi-allelic mutations of the ABCA3 gene represent the most frequent cause of …
ABCA3 [ATP-binding cassette (ABC), subfamily A, member 3] is a lung-specific phospholipid transporter critical for intracellular s
Performance of Candidate Serum Biomarkers for Systemic Sclerosis-Associated Interstitial Lung Disease.
Elhai M, Hoffmann-Vold AM, Avouac J, Pezet S, Cauvet A, Leblond A, Fretheim H, Garen T, Kuwana M, Molberg Ø, Allanore Y. Elhai M, et al. Arthritis Rheumatol. 2019 Jun;71(6):972-982. doi: 10.1002/art.40815. Epub 2019 Apr 26. Arthritis Rheumatol. 2019. PMID: 30624031
OBJECTIVE: Interstitial lung disease (ILD) in systemic sclerosis (SSc) runs a highly variable course, and prediction tools are highly desired. ...Lung fibrosis was measured by high-resolution computed tomography and pulmonary function tests. ...
OBJECTIVE: Interstitial lung disease (ILD) in systemic sclerosis (SSc) runs a highly variable course, and prediction to …
Pulmonary surfactant, lung function, and endobronchial inflammation in cystic fibrosis.
Griese M, Essl R, Schmidt R, Rietschel E, Ratjen F, Ballmann M, Paul K; BEAT Study Group. Griese M, et al. Am J Respir Crit Care Med. 2004 Nov 1;170(9):1000-5. doi: 10.1164/rccm.200405-575OC. Epub 2004 Jul 21. Am J Respir Crit Care Med. 2004. PMID: 15271694
Cystic fibrosis (CF) lung disease is primarily a disease of the small airways. We hypothesized that even in patients with normal lung function, a reduced surfactant function would be present and favor small airway obstruction. ...These findings in a large coh …
Cystic fibrosis (CF) lung disease is primarily a disease of the small airways. We hypothesized that even in patients with normal l
Tissue and Bronchoalveolar Lavage Biomarkers in Idiopathic Pulmonary Fibrosis Patients on Pirfenidone.
Ronan N, Bennett DM, Khan KA, McCarthy Y, Dahly D, Bourke L, Chelliah A, Cavazza A, O'Regan K, Moloney F, Plant BJ, Henry MT. Ronan N, et al. Lung. 2018 Oct;196(5):543-552. doi: 10.1007/s00408-018-0140-8. Epub 2018 Jul 31. Lung. 2018. PMID: 30066212
METHODS: Thirteen patients with confirmed idiopathic pulmonary fibrosis (IPF) underwent full physiological and radiological assessment at diagnosis and after 6-month pirfenidone therapy. ...We found an increase in three bronchoalveolar lavage angiogenesis cytokines, Placen …
METHODS: Thirteen patients with confirmed idiopathic pulmonary fibrosis (IPF) underwent full physiological and radiological assessmen …
Smoking reduces surfactant protein D and phospholipids in patients with and without chronic obstructive pulmonary disease.
Moré JM, Voelker DR, Silveira LJ, Edwards MG, Chan ED, Bowler RP. Moré JM, et al. BMC Pulm Med. 2010 Oct 25;10:53. doi: 10.1186/1471-2466-10-53. BMC Pulm Med. 2010. PMID: 20973980 Free PMC article.
BACKGROUND: Pulmonary surfactant D (SP-D) has important regulatory functions for innate immunity and has been implicated as a biomarker for chronic obstructive pulmonary disease (COPD). ...Among smokers with COPD, BAL SP-D correlated significantly with FEV1% …
BACKGROUND: Pulmonary surfactant D (SP-D) has important regulatory functions for innate immunity and has been implicated as a …
Protein expression profiling suggests relevance of noncanonical pathways in isolated pulmonary embolism.
Ten Cate V, Prochaska JH, Schulz A, Koeck T, Pallares Robles A, Lenz M, Eggebrecht L, Rapp S, Panova-Noeva M, Ghofrani HA, Meyer FJ, Espinola-Klein C, Lackner KJ, Michal M, Schuster AK, Strauch K, Zink AM, Laux V, Heitmeier S, Konstantinides SV, Münzel T, Andrade-Navarro MA, Leineweber K, Wild PS. Ten Cate V, et al. Blood. 2021 May 13;137(19):2681-2693. doi: 10.1182/blood.2019004571. Blood. 2021. PMID: 33529319 Free PMC article.
Patients with isolated pulmonary embolism (PE) have a distinct clinical profile from those with deep vein thrombosis (DVT)-associated PE, with more pulmonary conditions and atherosclerosis. ...Shared processes included upregulation of inflammation, response to oxida …
Patients with isolated pulmonary embolism (PE) have a distinct clinical profile from those with deep vein thrombosis (DVT)-associated …
Surfactant administration for neonatal respiratory distress does not improve lung interstitial fluid clearance: echographic and experimental evidence.
Cattarossi L, Copetti R, Poskurica B, Miserocchi G. Cattarossi L, et al. J Perinat Med. 2010 Sep;38(5):557-63. doi: 10.1515/jpm.2010.096. J Perinat Med. 2010. PMID: 20629494
In premature rabbits (28-29 days' gestational age), either receiving or not receiving surfactant, we followed the time course of lung water balance considering the wet weight/dry weight ratio, the morphology and compliance of alveoli and pulmonary inte …
In premature rabbits (28-29 days' gestational age), either receiving or not receiving surfactant, we followed the time course
58 results