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Inhaled Mannitol (Bronchitol) for Cystic Fibrosis.
Nolan SJ, Thornton J, Murray CS, Dwyer T. Nolan SJ, et al. Paediatr Respir Rev. 2016 Mar;18:52-4. doi: 10.1016/j.prrv.2015.12.001. Epub 2015 Dec 29. Paediatr Respir Rev. 2016. PMID: 26867712 Review. No abstract available.
Physiotherapy for cystic fibrosis in Australia and New Zealand: A clinical practice guideline.
Button BM, Wilson C, Dentice R, Cox NS, Middleton A, Tannenbaum E, Bishop J, Cobb R, Burton K, Wood M, Moran F, Black R, Bowen S, Day R, Depiazzi J, Doiron K, Doumit M, Dwyer T, Elliot A, Fuller L, Hall K, Hutchins M, Kerr M, Lee AL, Mans C, O'Connor L, Steward R, Potter A, Rasekaba T, Scoones R, Tarrant B, Ward N, West S, White D, Wilson L, Wood J, Holland AE. Button BM, et al. Respirology. 2016 May;21(4):656-67. doi: 10.1111/resp.12764. Epub 2016 Apr 18. Respirology. 2016. PMID: 27086904 Free PMC article.
CFTR Genotype and Maximal Exercise Capacity in Cystic Fibrosis: A Cross-sectional Study.
Radtke T, Hebestreit H, Gallati S, Schneiderman JE, Braun J, Stevens D, Hulzebos EH, Takken T, Boas SR, Urquhart DS, Lands LC, Tejero S, Sovtic A, Dwyer T, Petrovic M, Harris RA, Karila C, Savi D, Usemann J, Mei-Zahav M, Hatziagorou E, Ratjen F, Kriemler S; CFTR-Exercise study group. Radtke T, et al. Ann Am Thorac Soc. 2018 Feb;15(2):209-216. doi: 10.1513/AnnalsATS.201707-570OC. Epub 2017 Nov 15. Ann Am Thorac Soc. 2018. PMID: 29140739 Free article.
Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic Fibrosis.
Hebestreit H, Hulzebos EHJ, Schneiderman JE, Karila C, Boas SR, Kriemler S, Dwyer T, Sahlberg M, Urquhart DS, Lands LC, Ratjen F, Takken T, Varanistkaya L, Rücker V, Hebestreit A, Usemann J, Radtke T; Prognostic Value of CPET in CF Study Group. Hebestreit H, et al. Am J Respir Crit Care Med. 2019 Apr 15;199(8):987-995. doi: 10.1164/rccm.201806-1110OC. Am J Respir Crit Care Med. 2019. PMID: 30321487 Free article.
39 results