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2019 1
2020 37
2021 138
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Fungal lung disease.
Koltsida G, Zaoutis T. Koltsida G, et al. Paediatr Respir Rev. 2021 Mar;37:99-104. doi: 10.1016/j.prrv.2020.04.009. Epub 2020 Apr 22. Paediatr Respir Rev. 2021. PMID: 32527608 Review.
Fungal lung disease in the paediatric population occurs with distinct features in the immunocompetent, in immunocompromised patients and in people with cystic fibrosis. Pulmonary mycoses are the least prevalent in immunocompetent children, with the most common disea …
Fungal lung disease in the paediatric population occurs with distinct features in the immunocompetent, in immunocompromised patients and in …
WNT-β-catenin signalling - a versatile player in kidney injury and repair.
Schunk SJ, Floege J, Fliser D, Speer T. Schunk SJ, et al. Nat Rev Nephrol. 2021 Mar;17(3):172-184. doi: 10.1038/s41581-020-00343-w. Epub 2020 Sep 28. Nat Rev Nephrol. 2021. PMID: 32989282 Review.
Transient WNT-beta-catenin activation stimulates tissue regeneration after acute kidney injury, whereas sustained (uncontrolled) WNT-beta-catenin signalling promotes kidney fibrosis in chronic kidney disease (CKD), podocyte injury and proteinuria, persistent tissue damage …
Transient WNT-beta-catenin activation stimulates tissue regeneration after acute kidney injury, whereas sustained (uncontrolled) WNT-beta-ca …
Macrophage dysfunction in cystic fibrosis: Nature or nurture?
Turton KB, Ingram RJ, Valvano MA. Turton KB, et al. J Leukoc Biol. 2021 Mar;109(3):573-582. doi: 10.1002/JLB.4RU0620-245R. Epub 2020 Jul 17. J Leukoc Biol. 2021. PMID: 32678926 Review.
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) affect the homeostasis of chloride flux by epithelial cells. This has deleterious consequences, especially in respiratory epithelia, where the defect results in mucus accumulation distinctiv …
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) affect the homeostasis of chloride flux by epithel …
Noninvasive Ventilation in Cystic Fibrosis: Clinical Indications and Outcomes in a Large UK Adult Cystic Fibrosis Center.
Spoletini G, Pollard K, Watson R, Darby MJ, Johnstone A, Etherington C, Whitaker P, Clifton IJ, Peckham DG. Spoletini G, et al. Respir Care. 2021 Mar;66(3):466-474. doi: 10.4187/respcare.07862. Epub 2020 Sep 8. Respir Care. 2021. PMID: 32900912
BACKGROUND: Noninvasive ventilation (NIV) is routinely used to treat patients with cystic fibrosis and respiratory failure. However, evidence on its use is limited, with no data on its role in disease progression and outcomes. ...All patients with cystic f
BACKGROUND: Noninvasive ventilation (NIV) is routinely used to treat patients with cystic fibrosis and respiratory failure. Ho …
Living and dying with cystic fibrosis.
Miller M. Miller M. BMJ Support Palliat Care. 2021 Mar;11(1):86-88. doi: 10.1136/bmjspcare-2020-002631. Epub 2020 Sep 11. BMJ Support Palliat Care. 2021. PMID: 32917651 No abstract available.
Redesign of the Australian Cystic Fibrosis Data Registry: A multidisciplinary collaboration.
Ahern S, Dean J, Liman J, Ruseckaite R, Burke N, Gollan M, Keatley L, King S, Kotsimbos T, Middleton PG, Schultz A, Wainwright C, Wark P, Bell S. Ahern S, et al. Paediatr Respir Rev. 2021 Mar;37:37-43. doi: 10.1016/j.prrv.2020.03.001. Epub 2020 Mar 26. Paediatr Respir Rev. 2021. PMID: 32331762 Review.
Clinical registries that monitor and review outcomes for patients with cystic fibrosis have existed internationally for many decades. However, their purpose continues to evolve and now includes the capability to support clinical effectiveness research, clinical tria …
Clinical registries that monitor and review outcomes for patients with cystic fibrosis have existed internationally for many d …
Pathways, practices and architectures: Containing antimicrobial resistance in the cystic fibrosis clinic.
Brown N, Buse C, Lewis A, Martin D, Nettleton S. Brown N, et al. Health (London). 2021 Mar;25(2):196-213. doi: 10.1177/1363459319866894. Epub 2019 Aug 7. Health (London). 2021. PMID: 31387378
Preventing antimicrobial resistance and cross-infection in cystic fibrosis increasingly depends on the spatiotemporal isolation of both people and pathogens. ...Finally, we take up the question of air, the intangibility of airborne risks and their material mitigatio …
Preventing antimicrobial resistance and cross-infection in cystic fibrosis increasingly depends on the spatiotemporal isolatio …
Molar mass effect in food and health.
Nishinari K, Fang Y. Nishinari K, et al. Food Hydrocoll. 2021 Mar;112:106110. doi: 10.1016/j.foodhyd.2020.106110. Epub 2020 Sep 3. Food Hydrocoll. 2021. PMID: 32895590 Free PMC article. Review.
In these functions, the molar mass is one of the key factors, and therefore, the effects of molar mass on various health problems related to noncommunicable diseases or symptoms such as cancer, hyperlipidemia, hyperglycemia, constipation, high blood pressure, knee pain, osteoporo …
In these functions, the molar mass is one of the key factors, and therefore, the effects of molar mass on various health problems related to …
A bird eye view on cystic fibrosis: An underestimated multifaceted chronic disorder.
Kotnala S, Dhasmana A, Kashyap VK, Chauhan SC, Yallapu MM, Jaggi M. Kotnala S, et al. Life Sci. 2021 Mar 1;268:118959. doi: 10.1016/j.lfs.2020.118959. Epub 2020 Dec 28. Life Sci. 2021. PMID: 33383045 Review.
Cystic fibrosis (CF) is an autosomal recessive disease which involves the mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. ...
Cystic fibrosis (CF) is an autosomal recessive disease which involves the mutations in the cystic fibrosis trans
Cystic fibrosis newborn screening: the importance of bloodspot sample quality.
Doull I, Course CW, Hanks RE, Southern KW, Forton JT, Thia LP, Moat SJ. Doull I, et al. Arch Dis Child. 2021 Mar;106(3):253-257. doi: 10.1136/archdischild-2020-318999. Epub 2020 Aug 28. Arch Dis Child. 2021. PMID: 32859613
OBJECTIVE: Wales has an immunoreactive trypsin (IRT)-DNA cystic fibrosis (CF) newborn screening (NBS) programme. Most CF NBS false negative cases are due to an IRT concentration below the screening threshold. ...Eighteen potential false negatives were identified, of …
OBJECTIVE: Wales has an immunoreactive trypsin (IRT)-DNA cystic fibrosis (CF) newborn screening (NBS) programme. Most CF NBS f …
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