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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 4
1964 12
1968 2
1971 1
1972 1
1973 2
1974 2
1975 1
1977 1
1978 1
1979 4
1980 2
1981 3
1982 2
1983 6
1984 6
1985 7
1986 6
1987 7
1988 9
1989 7
1990 5
1991 13
1992 16
1993 13
1994 15
1995 24
1996 19
1997 24
1998 13
1999 22
2000 17
2001 29
2002 21
2003 37
2004 31
2005 44
2006 49
2007 62
2008 46
2009 45
2010 59
2011 58
2012 73
2013 80
2014 99
2015 90
2016 118
2017 107
2018 123
2019 123
2020 147
2021 129
2022 135
2023 110
2024 104
2025 16

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1,927 results

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Page 1
Factors Associated With Multi-Drug Resistant Organisms Among Bronchiectasis Patients: A Retrospective Study of Bronchiectasis Patients in Jordan.
Al Oweidat K, Toubasi AA, Khraisat FA, Al-Sayegh TN, Al-Harasis LM, Albtoosh AS. Al Oweidat K, et al. Int J Gen Med. 2025 Jan 25;18:391-402. doi: 10.2147/IJGM.S490196. eCollection 2025. Int J Gen Med. 2025. PMID: 39881954 Free PMC article.
BACKGROUND: Bronchiectasis, a respiratory ailment, significantly impacts the life expectancy of individuals. ...METHODS: A retrospective observational analysis was conducted on adult bronchiectasis patients attending clinics at Jordan University Hospital. The diagno …
BACKGROUND: Bronchiectasis, a respiratory ailment, significantly impacts the life expectancy of individuals. ...METHODS: A retrospect …
Application of low-dose FDG-PET/MRI for quantification of lung changes in pediatric patients with cystic fibrosis: a new inflammatory index.
Schwarz R, Schäfer JF, Utz P, Graepler-Mainka U, Dittmann H, Kraus MS, Esser M. Schwarz R, et al. Quant Imaging Med Surg. 2025 Jan 2;15(1):189-202. doi: 10.21037/qims-24-989. Epub 2024 Dec 30. Quant Imaging Med Surg. 2025. PMID: 39838989 Free PMC article.
BACKGROUND: Clinical severity and progression of lung disease in cystic fibrosis (CF) are significantly influenced by the degree of lung inflammation. ...Therefore, the present study assesses the quantification of inflammatory lung changes using …
BACKGROUND: Clinical severity and progression of lung disease in cystic fibrosis (CF) are significantly influenced by t …
Successful Treatment of a Patient With Chronic Bronchiectasis Using an Induced Native Phage Cocktail: A Case Report.
Jernigan DA, Hentish RD. Jernigan DA, et al. Cureus. 2025 Jan 19;17(1):e77681. doi: 10.7759/cureus.77681. eCollection 2025 Jan. Cureus. 2025. PMID: 39834667 Free PMC article.
Bronchiectasis is a well-recognized chronic respiratory disease characterized by a productive cough and multi-microbial activation syndrome (MMAS) of various respiratory infections due to what can be the permanent dilatation of the bronchi. ...The introduction of In
Bronchiectasis is a well-recognized chronic respiratory disease characterized by a productive cough and multi-microbial activation sy
Nanoscale Viscometry Reveals an Inherent Mucus Defect in Cystic Fibrosis.
Ponomarchuk O, Boudreault F, Gryczynski I, Lee B, Dzyuba SV, Fudala R, Gryczynski Z, Hanrahan JW, Grygorczyk R. Ponomarchuk O, et al. ACS Nano. 2025 Feb 4;19(4):4637-4649. doi: 10.1021/acsnano.4c14927. Epub 2025 Jan 18. ACS Nano. 2025. PMID: 39825840
The abnormally viscous and thick mucus is a hallmark of cystic fibrosis (CF). How the mutated CF gene causes abnormal mucus remains an unanswered question of paramount interest. ...It encourages the development of therapeutics that target presecretory mechanisms in …
The abnormally viscous and thick mucus is a hallmark of cystic fibrosis (CF). How the mutated CF gene causes abnormal mucus re …
Establishment of a 3D-Printed Tissue-on-a-Chip Model for Live Imaging of Bacterial Infections.
Fuglsang-Madsen A, Haagensen JAJ, De Rudder C, Simões FB, Molin S, Johansen HK. Fuglsang-Madsen A, et al. Adv Exp Med Biol. 2025 Jan 18. doi: 10.1007/5584_2024_829. Online ahead of print. Adv Exp Med Biol. 2025. PMID: 39825043
In this communication, we briefly present existing in vivo models for cystic fibrosis and their limitations in replicating human respiratory infections. We then present a novel, 3D-printed, cytocompatible microfluidic lung-on-a-chip device, designed to simula …
In this communication, we briefly present existing in vivo models for cystic fibrosis and their limitations in replicating hum …
Baseline characteristics of patients in the Chinese Bronchiectasis Registry (BE-China): a multicentre prospective cohort study.
Xu JF, Zheng HZ, Lu HW, Wang LW, Wu B, Lv XD, Luo H, Feng J, Li YY, Liu L, Jia JG, Mo WQ, Gu HY, Jiang JB, Wang DX, Wang B, Li L, Yuan Z, Li W, Xie M, Jie ZJ, Fan XY, Li D, Tian X, Zhang M, Guan WJ, Fan H, Song YL, He J, Chu DJ, Du CL, Zhang JQ, Cao C, Qu JM, Chalmers JD; BE-China Registry Investigators. Xu JF, et al. Lancet Respir Med. 2025 Feb;13(2):166-176. doi: 10.1016/S2213-2600(24)00364-3. Epub 2025 Jan 10. Lancet Respir Med. 2025. PMID: 39805296 Free article.
We aimed to describe the clinical characteristics of patients with bronchiectasis in China. METHODS: The Chinese Bronchiectasis Registry (BE-China) is a prospective, observational cohort enrolling patients from 111 hospitals in China. Data on demographics, comorbidi …
We aimed to describe the clinical characteristics of patients with bronchiectasis in China. METHODS: The Chinese Bronchiectasis
Association Between Lung Parenchymal Attenuation in Computed Tomography and Airflow Limitation in Adults with Cystic Fibrosis.
Esteban Baloira L, Zamarrón de Lucas E, Segura CC, Lerín Baratas M, Fernández Velilla M, Torres Sánchez MI, Pinilla Fernández I, Mariscal Aguilar P, Álvarez-Sala Walther R, Prados Sánchez C. Esteban Baloira L, et al. Diagnostics (Basel). 2025 Jan 4;15(1):107. doi: 10.3390/diagnostics15010107. Diagnostics (Basel). 2025. PMID: 39795635 Free PMC article.
Objectives: To determine the association between airflow limitation and the quantification of lung attenuation in computed tomography (CT) in adult patients with cystic fibrosis (CF). ...We collected clinical data and the results of spiro …
Objectives: To determine the association between airflow limitation and the quantification of lung attenuation in computed
Introduction of Ivacaftor/Lumacaftor in Children With Cystic Fibrosis Homozygous for F508del in the Netherlands: A Nationwide Real-Life Study.
Zwitserloot AM, Aziz SZ, Chen Y, Bannier MAGE, Janssens HM, Merkus PFJM, Nuijsink M, Terheggen-Lagro SWJ, Tiddens HAWM, Zomer-van Ommen DD, Vonk JM, de Winter-de Groot KM, Willemse BWM, Koppelman GH. Zwitserloot AM, et al. Pediatr Pulmonol. 2025 Jan;60(1):e27473. doi: 10.1002/ppul.27473. Pediatr Pulmonol. 2025. PMID: 39785291 Free PMC article.
We investigated 1-year efficacy of lum/iva on lung function and small airway and structural lung disease evaluated by multiple breath nitrogen washout and CT scan. ...In a subgroup, markers of small airway function and structural lung disease, such as …
We investigated 1-year efficacy of lum/iva on lung function and small airway and structural lung disease evaluated by multiple …
Airway Remodeling in Cystic Fibrosis Is Heterogeneous.
Vermaut A, Geudens V, Willems L, Aerts G, Kerckhof P, Hooft C, Beeckmans H, Kaes J, Jin X, De Fays C, Mohamady Y, Van Slambrouck J, Aversa L, Verhaegen J, Cortesi EE, Weynand B, Boone MN, McDonough JE, Van Raemdonck DE, Ceulemans LJ, Wuyts WA, Vos R, Gayan-Ramirez G, Vermeulen F, Proesmans M, Vanaudenaerde BM, Dupont LJ, Boon M. Vermaut A, et al. Ann Am Thorac Soc. 2024 Dec 19. doi: 10.1513/AnnalsATS.202404-446OC. Online ahead of print. Ann Am Thorac Soc. 2024. PMID: 39700513
RATIONALE+OBJECTIVE/ Cystic fibrosis (CF) is characterized by bronchiectasis on imaging, while functionally evolving towards obstructive impairment. Despite its assumed importance in CF, small airway remodeling and its relation to bronchiectasis
RATIONALE+OBJECTIVE/ Cystic fibrosis (CF) is characterized by bronchiectasis on imaging, while functionally evol …
1,927 results