Bye PT - Search Results

1

Adults with cystic fibrosis prefer hypertonic saline before or during airway clearance techniques: a randomised crossover trial.

Dentice RL, Elkins MR, Bye PT. Dentice RL, et al. Among authors: bye pt. J Physiother. 2012;58(1):33-40. doi: 10.1016/S1836-9553(12)70070-X. J Physiother. 2012. PMID: 22341380 Free article. Clinical Trial.

2

Cystic fibrosis and pregnancy.

Jankelson D, Robinson M, Parsons S, Torzillo P, Peat B, Bye P. Jankelson D, et al. Aust N Z J Obstet Gynaecol. 1998 May;38(2):180-4. doi: 10.1111/j.1479-828x.1998.tb02997.x. Aust N Z J Obstet Gynaecol. 1998. PMID: 9653856

3

Osmotic stimuli increase clearance of mucus in patients with mucociliary dysfunction.

Daviskas E, Robinson M, Anderson SD, Bye PT. Daviskas E, et al. Among authors: bye pt. J Aerosol Med. 2002 Fall;15(3):331-41. doi: 10.1089/089426802760292681. J Aerosol Med. 2002. PMID: 12396422 Review.

4

Arm positioning alters lung volumes in subjects with COPD and healthy subjects.

McKeough ZJ, Alison JA, Bye PT. McKeough ZJ, et al. Among authors: bye pt. Aust J Physiother. 2003;49(2):133-7. doi: 10.1016/s0004-9514(14)60129-x. Aust J Physiother. 2003. PMID: 12775208 Clinical Trial.

5

Method for detection of respiratory viruses in the sputa of patients with cystic fibrosis.

Punch G, Syrmis MW, Rose BR, Harbour C, Bye PT, Nissen MD, Elkins MR, Sloots TP. Punch G, et al. Among authors: bye pt. Eur J Clin Microbiol Infect Dis. 2005 Jan;24(1):54-7. doi: 10.1007/s10096-004-1273-7. Eur J Clin Microbiol Infect Dis. 2005. PMID: 15616837 Free PMC article.

6

Effect of body position on maximal expiratory pressure and flow in adults with cystic fibrosis.

Elkins MR, Alison JA, Bye PT. Elkins MR, et al. Among authors: bye pt. Pediatr Pulmonol. 2005 Nov;40(5):385-91. doi: 10.1002/ppul.20287. Pediatr Pulmonol. 2005. PMID: 16130087 Clinical Trial.

7

Effect of airway clearance techniques on the efficacy of the sputum induction procedure.

Elkins MR, Lane T, Goldberg H, Pagliuso J, Garske LA, Hector E, Marchetto L, Alison JA, Bye PT. Elkins MR, et al. Among authors: bye pt. Eur Respir J. 2005 Nov;26(5):904-8. doi: 10.1183/09031936.05.00033105. Eur Respir J. 2005. PMID: 16264054 Free article. Clinical Trial.

8

A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis.

Elkins MR, Robinson M, Rose BR, Harbour C, Moriarty CP, Marks GB, Belousova EG, Xuan W, Bye PT; National Hypertonic Saline in Cystic Fibrosis (NHSCF) Study Group. Elkins MR, et al. Among authors: bye pt. N Engl J Med. 2006 Jan 19;354(3):229-40. doi: 10.1056/NEJMoa043900. N Engl J Med. 2006. PMID: 16421364 Free article. Clinical Trial.

9

Inhaled hypertonic saline as a therapy for cystic fibrosis.

Elkins MR, Bye PT. Elkins MR, et al. Among authors: bye pt. Curr Opin Pulm Med. 2006 Nov;12(6):445-52. doi: 10.1097/01.mcp.0000245714.89632.b2. Curr Opin Pulm Med. 2006. PMID: 17053496 Review.

10

Other mucoactive agents for cystic fibrosis.

Bye PT, Elkins MR. Bye PT, et al. Paediatr Respir Rev. 2007 Mar;8(1):30-9. doi: 10.1016/j.prrv.2007.02.008. Epub 2007 Mar 26. Paediatr Respir Rev. 2007. PMID: 17419976 Review.

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