Lannefors L - Search Results

1

Lung function in the aging Swedish cystic fibrosis population.

Dennersten U, Lannefors L, Höglund P, Hellberg K, Johansson H, Lagerkvist AL, Ortfelt M, Sahlberg M, Eriksson L. Dennersten U, et al. Among authors: lannefors l. Respir Med. 2009 Jul;103(7):1076-82. doi: 10.1016/j.rmed.2009.01.020. Epub 2009 Feb 23. Respir Med. 2009. PMID: 19233629 Free article.

2

Demographic transition of the Swedish cystic fibrosis community--results of modern care.

Lannefors L, Lindgren A. Lannefors L, et al. Respir Med. 2002 Sep;96(9):681-5. doi: 10.1053/rmed.2002.1329. Respir Med. 2002. PMID: 12243313 Free article.

3

Mucus clearance with three chest physiotherapy regimes in cystic fibrosis: a comparison between postural drainage, PEP and physical exercise.

Lannefors L, Wollmer P. Lannefors L, et al. Eur Respir J. 1992 Jun;5(6):748-53. Eur Respir J. 1992. PMID: 1628733

4

Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I.

Schaedel C, Andersson AM, Kristoffersson AC, Kornfält R, Lannefors L, Holmberg L. Schaedel C, et al. Among authors: lannefors l. Clin Genet. 1998 May;53(5):383-6. doi: 10.1111/j.1399-0004.1998.tb02750.x. Clin Genet. 1998. PMID: 9660057

5

Physiotherapy in infants and young children with cystic fibrosis: current practice and future developments.

Lannefors L, Button BM, McIlwaine M. Lannefors L, et al. J R Soc Med. 2004;97 Suppl 44(Suppl 44):8-25. J R Soc Med. 2004. PMID: 15239290 Free PMC article. Review. No abstract available.

6

Thoracic configuration in patients ageing with cystic fibrosis: A retrospective single-blinded cohort study.

Sinderholm Sposato N, Rossi Norrlund R, Gilljam M, Bjerså K, Lannefors L, Fagevik Olsén M. Sinderholm Sposato N, et al. Among authors: lannefors l. Respir Physiol Neurobiol. 2023 Jan;307:103976. doi: 10.1016/j.resp.2022.103976. Epub 2022 Oct 4. Respir Physiol Neurobiol. 2023. PMID: 36206973 Free article. Clinical Trial.

7

Positive expiratory pressure - Common clinical applications and physiological effects.

Fagevik Olsén M, Lannefors L, Westerdahl E. Fagevik Olsén M, et al. Among authors: lannefors l. Respir Med. 2015 Mar;109(3):297-307. doi: 10.1016/j.rmed.2014.11.003. Epub 2014 Nov 12. Respir Med. 2015. PMID: 25573419 Free article. Review.

8

The neutrophil-recruiting chemokine GCP-2/CXCL6 is expressed in cystic fibrosis airways and retains its functional properties after binding to extracellular DNA.

Jovic S, Linge HM, Shikhagaie MM, Olin AI, Lannefors L, Erjefält JS, Mörgelin M, Egesten A. Jovic S, et al. Among authors: lannefors l. Mucosal Immunol. 2016 Jan;9(1):112-23. doi: 10.1038/mi.2015.43. Epub 2015 May 20. Mucosal Immunol. 2016. PMID: 25993443 Free article.

9

Identification of MUC5B, MUC5AC and small amounts of MUC2 mucins in cystic fibrosis airway secretions.

Davies JR, Svitacheva N, Lannefors L, Kornfält R, Carlstedt I. Davies JR, et al. Among authors: lannefors l. Biochem J. 1999 Dec 1;344 Pt 2(Pt 2):321-30. Biochem J. 1999. PMID: 10567212 Free PMC article.

10

Physical activity assessment in cystic fibrosis: A position statement.

Bradley J, O'Neill B, Kent L, Hulzebos EH, Arets B, Hebestreit H; Exercise Working Group European CF Society, for publication in Journal of CF; Exercise Working Group European CF Society. Bradley J, et al. J Cyst Fibros. 2015 Nov;14(6):e25-32. doi: 10.1016/j.jcf.2015.05.011. Epub 2015 Jul 26. J Cyst Fibros. 2015. PMID: 26219990 Free article. Review.

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