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Items: 1 to 50 of 164

1.

Side lying during nebulisation can significantly improve apical deposition in healthy adults and adults with mild cystic fibrosis lung disease: a randomised crossover trial.

Dentice RL, Elkins MR, Verschuer J, Eberl S, Dwyer G, Bye PTP.

BMC Pulm Med. 2019 Jul 16;19(1):128. doi: 10.1186/s12890-019-0886-7.

2.

Non-invasive ventilation versus oxygen therapy in cystic fibrosis: A 12-month randomized trial.

Milross MA, Piper AJ, Dwyer TJ, Wong K, Bell SC, Bye PTP; Non-Invasive Ventilation in Cystic Fibrosis (NIVCF) Study Group.

Respirology. 2019 Jun 17. doi: 10.1111/resp.13604. [Epub ahead of print]

PMID:
31206975
3.

Effects of exercise and airway clearance (positive expiratory pressure) on mucus clearance in cystic fibrosis: a randomised crossover trial.

Dwyer TJ, Daviskas E, Zainuldin R, Verschuer J, Eberl S, Bye PTP, Alison JA.

Eur Respir J. 2019 Apr 18;53(4). pii: 1801793. doi: 10.1183/13993003.01793-2018. Print 2019 Apr.

PMID:
30846472
4.

Management of bronchiectasis in adults.

Visser SK, Bye P, Morgan L.

Med J Aust. 2018 Aug 20;209(4):177-183. Review.

PMID:
30107772
5.

Use of extracorporeal membrane oxygenation in cystic fibrosis in an Australian cystic fibrosis centre.

Sivam S, Dentice R, Reddy N, Moriarty C, Yozghatlian V, Mellis C, Torzillo P, Glanville A, Gattas D, Bye P.

Intern Med J. 2018 Mar;48(3):340-343. doi: 10.1111/imj.13728.

PMID:
29512325
6.
7.

Hypoglycaemia in cystic fibrosis: An analysis of a single centre adult cystic fibrosis clinic.

Armaghanian N, Markovic TP, Brand-Miller JC, Bye PTP, Moriarty CP, Steinbeck KS.

J Cyst Fibros. 2018 Jul;17(4):542-547. doi: 10.1016/j.jcf.2017.11.015. Epub 2017 Dec 16.

PMID:
29254823
8.

Effects of treadmill exercise versus Flutter® on respiratory flow and sputum properties in adults with cystic fibrosis: a randomised, controlled, cross-over trial.

Dwyer TJ, Zainuldin R, Daviskas E, Bye PT, Alison JA.

BMC Pulm Med. 2017 Jan 11;17(1):14. doi: 10.1186/s12890-016-0360-8.

9.

Bilateral adrenal haemorrhages: a crucial incidental finding.

Cho SM, Bye P.

BJR Case Rep. 2016 Dec 8;3(2):20160107. doi: 10.1259/bjrcr.20160107. eCollection 2017.

10.

Liver and lung transplantation in cystic fibrosis: an adult cystic fibrosis centre's experience.

Sivam S, Al-Hindawi Y, Di Michiel J, Moriarty C, Spratt P, Jansz P, Malouf M, Plit M, Pleass H, Havryk A, Bowen D, Haber P, Glanville AR, Bye PT.

Intern Med J. 2016 Jul;46(7):852-4. doi: 10.1111/imj.13126.

PMID:
27405894
11.

A randomised trial of hypertonic saline during hospitalisation for exacerbation of cystic fibrosis.

Dentice RL, Elkins MR, Middleton PG, Bishop JR, Wark PA, Dorahy DJ, Harmer CJ, Hu H, Bye PT.

Thorax. 2016 Feb;71(2):141-7. doi: 10.1136/thoraxjnl-2014-206716.

PMID:
26769016
12.

Exercise training to improve exercise capacity and quality of life in people with non-malignant dust-related respiratory diseases.

Dale MT, McKeough ZJ, Troosters T, Bye P, Alison JA.

Cochrane Database Syst Rev. 2015 Nov 5;(11):CD009385. doi: 10.1002/14651858.CD009385.pub2. Review.

PMID:
26544672
13.

Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: a randomised trial.

Dwyer TJ, Robbins L, Kelly P, Piper AJ, Bell SC, Bye PT.

J Physiother. 2015 Jul;61(3):142-7. doi: 10.1016/j.jphys.2015.05.019. Epub 2015 Jun 18.

14.

Physical activity in people with asbestos related pleural disease and dust-related interstitial lung disease: An observational study.

Dale MT, McKeough ZJ, Munoz PA, Corte P, Bye PT, Alison JA.

Chron Respir Dis. 2015 Nov;12(4):291-8. doi: 10.1177/1479972315587518. Epub 2015 Jun 5.

PMID:
26048393
15.

Exercise training for asbestos-related and other dust-related respiratory diseases: a randomised controlled trial.

Dale MT, McKeough ZJ, Munoz PA, Corte P, Bye PT, Alison JA.

BMC Pulm Med. 2014 Nov 18;14:180. doi: 10.1186/1471-2466-14-180.

16.

Spontaneous coronary artery dissection associated with coughing.

Sivam S, Yozghatlian V, Dentice R, McGrady M, Moriarty C, Di Michiel J, Bye PT, Rees D.

J Cyst Fibros. 2014 Mar;13(2):235-7. doi: 10.1016/j.jcf.2013.10.003. Epub 2013 Oct 21. No abstract available.

17.

Modulation of gene expression by Pseudomonas aeruginosa during chronic infection in the adult cystic fibrosis lung.

Harmer C, Alnassafi K, Hu H, Elkins M, Bye P, Rose B, Cordwell S, Triccas JA, Harbour C, Manos J.

Microbiology. 2013 Nov;159(Pt 11):2354-63. doi: 10.1099/mic.0.066985-0. Epub 2013 Sep 6.

PMID:
24014664
18.

Functional exercise capacity and health-related quality of life in people with asbestos related pleural disease: an observational study.

Dale MT, McKeough ZJ, Munoz PA, Corte P, Bye PT, Alison JA.

BMC Pulm Med. 2013 Jan 10;13:1. doi: 10.1186/1471-2466-13-1.

19.

Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres.

Kidd TJ, Ramsay KA, Hu H, Marks GB, Wainwright CE, Bye PT, Elkins MR, Robinson PJ, Rose BR, Wilson JW, Grimwood K, Bell SC; ACPinCF Investigator Group.

Eur Respir J. 2013 May;41(5):1091-100. doi: 10.1183/09031936.00060512. Epub 2012 Aug 9.

20.

Pseudomonas aeruginosa strains from the chronically infected cystic fibrosis lung display increased invasiveness of A549 epithelial cells over time.

Harmer CJ, Triccas JA, Hu H, Rose B, Bye P, Elkins M, Manos J.

Microb Pathog. 2012 Jul;53(1):37-43. doi: 10.1016/j.micpath.2012.03.011. Epub 2012 Apr 10.

PMID:
22516803
21.

Arm exercise training in chronic obstructive pulmonary disease: a randomised controlled trial.

McKeough ZJ, Bye PT, Alison JA.

Chron Respir Dis. 2012 Aug;9(3):153-62. doi: 10.1177/1479972312440814. Epub 2012 Mar 27.

PMID:
22452973
22.

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

Dentice RL, Elkins MR, Bye PT.

J Physiother. 2012;58(1):33-40. doi: 10.1016/S1836-9553(12)70070-X.

23.

Cystic fibrosis in Australia, 2009: results from a data registry.

Bell SC, Bye PT, Cooper PJ, Martin AJ, McKay KO, Robinson PJ, Ryan GF, Sims GC.

Med J Aust. 2011 Oct 3;195(7):396-400.

PMID:
21978347
24.

Pseudomonas aeruginosa AES-1 exhibits increased virulence gene expression during chronic infection of cystic fibrosis lung.

Naughton S, Parker D, Seemann T, Thomas T, Turnbull L, Rose B, Bye P, Cordwell S, Whitchurch C, Manos J.

PLoS One. 2011;6(9):e24526. doi: 10.1371/journal.pone.0024526. Epub 2011 Sep 15.

25.

The role of exercise in maintaining health in cystic fibrosis.

Dwyer TJ, Elkins MR, Bye PT.

Curr Opin Pulm Med. 2011 Nov;17(6):455-60. doi: 10.1097/MCP.0b013e32834b6af4. Review.

PMID:
21881514
26.

Mechanisms and applications of hypertonic saline.

Elkins MR, Bye PT.

J R Soc Med. 2011 Jul;104 Suppl 1:S2-5. doi: 10.1258/jrsm.2011.s11101. Review. No abstract available.

27.

Pregnancy outcomes in the current era of cystic fibrosis care: a 15-year experience.

Lau EM, Barnes DJ, Moriarty C, Ogle R, Dentice R, Civitico J, Avedello A, Torzillo PJ, Bye PT.

Aust N Z J Obstet Gynaecol. 2011 Jun;51(3):220-4. doi: 10.1111/j.1479-828X.2010.01287.x. Epub 2011 Feb 7.

PMID:
21631440
28.

Difficult asthma and Churg-Strauss-like syndrome: a cautionary tale.

Lau EM, Cooper W, Bye PT, Yan K.

Respirology. 2011 Jan;16(1):180-1. doi: 10.1111/j.1440-1843.2010.01884.x. No abstract available.

PMID:
21504509
29.

Gas exchange in disease: asthma, chronic obstructive pulmonary disease, cystic fibrosis, and interstitial lung disease.

Young IH, Bye PT.

Compr Physiol. 2011 Apr;1(2):663-97. doi: 10.1002/cphy.c090012. Review.

PMID:
23737199
30.

Effects of exercise on respiratory flow and sputum properties in patients with cystic fibrosis.

Dwyer TJ, Alison JA, McKeough ZJ, Daviskas E, Bye PTP.

Chest. 2011 Apr;139(4):870-877. doi: 10.1378/chest.10-1158. Epub 2010 Sep 9.

PMID:
20829339
31.

Clinical profile of adult cystic fibrosis patients with frequent epidemic clones of Pseudomonas aeruginosa.

Tingpej P, Elkins M, Rose B, Hu H, Moriarty C, Manos J, Barras B, Bye P, Harbour C.

Respirology. 2010 Aug;15(6):923-9. doi: 10.1111/j.1440-1843.2010.01792.x. Epub 2010 Jun 21.

PMID:
20573059
32.

Pregnancy and cystic fibrosis.

Lau EM, Moriarty C, Ogle R, Bye PT.

Paediatr Respir Rev. 2010 Jun;11(2):90-4. doi: 10.1016/j.prrv.2010.01.008. Epub 2010 Feb 25. Review.

PMID:
20416544
33.

Multi-centre research in Australia: analysis of a recent National Health and Medical Research Council-funded project.

Kidd TJ, Marks GB, Bye PT, Wainwright CE, Robinson PJ, Rose BR, Harbour C, Bell SC; ACPinCF INVESTIGATORS.

Respirology. 2009 Sep;14(7):1051-5. doi: 10.1111/j.1440-1843.2009.01595.x.

PMID:
19740265
34.

Randomized trial of a decision aid for patients with cystic fibrosis considering lung transplantation.

Vandemheen KL, O'Connor A, Bell SC, Freitag A, Bye P, Jeanneret A, Berthiaume Y, Brown N, Wilcox P, Ryan G, Brager N, Rabin H, Morrison N, Gibson P, Jackson M, Paterson N, Middleton P, Aaron SD.

Am J Respir Crit Care Med. 2009 Oct 15;180(8):761-8. doi: 10.1164/rccm.200903-0421OC. Epub 2009 Jul 9.

PMID:
19590021
35.

Recombinant activated factor VII for massive hemoptysis in patients with cystic fibrosis.

Lau EMT, Yozghatlian V, Kosky C, Moriarty C, Dentice R, Waugh R, Torzillo PJ, Bye PT.

Chest. 2009 Jul;136(1):277-281. doi: 10.1378/chest.08-2948.

PMID:
19584209
36.

Sexual and reproductive health in men with cystic fibrosis: consistent preferences, inconsistent practices.

Sawyer SM, Farrant B, Wilson J, Ryan G, O'Carroll M, Bye P, Bell S.

J Cyst Fibros. 2009 Jul;8(4):264-9. doi: 10.1016/j.jcf.2009.05.005. Epub 2009 Jun 12.

37.

Evaluation of the SenseWear activity monitor during exercise in cystic fibrosis and in health.

Dwyer TJ, Alison JA, McKeough ZJ, Elkins MR, Bye PT.

Respir Med. 2009 Oct;103(10):1511-7. doi: 10.1016/j.rmed.2009.04.013. Epub 2009 May 23.

38.

Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients.

Kidd TJ, Ramsay KA, Hu H, Bye PT, Elkins MR, Grimwood K, Harbour C, Marks GB, Nissen MD, Robinson PJ, Rose BR, Sloots TP, Wainwright CE, Bell SC; ACPinCF Investigators.

J Clin Microbiol. 2009 May;47(5):1503-9. doi: 10.1128/JCM.00014-09. Epub 2009 Mar 4.

39.

Gene expression characteristics of a cystic fibrosis epidemic strain of Pseudomonas aeruginosa during biofilm and planktonic growth.

Manos J, Arthur J, Rose B, Bell S, Tingpej P, Hu H, Webb J, Kjelleberg S, Gorrell MD, Bye P, Harbour C.

FEMS Microbiol Lett. 2009 Mar;292(1):107-14. doi: 10.1111/j.1574-6968.2008.01472.x.

40.

Phonetic duration, phonological quantity and prosodic structure in Inari Saami.

Bye P, Sagulin E, Toivonen I.

Phonetica. 2009;66(4):199-221. doi: 10.1159/000298583. Epub 2010 Apr 23.

PMID:
20431321
41.

Transcriptome analyses and biofilm-forming characteristics of a clonal Pseudomonas aeruginosa from the cystic fibrosis lung.

Manos J, Arthur J, Rose B, Tingpej P, Fung C, Curtis M, Webb JS, Hu H, Kjelleberg S, Gorrell MD, Bye P, Harbour C.

J Med Microbiol. 2008 Dec;57(Pt 12):1454-65. doi: 10.1099/jmm.0.2008/005009-0.

PMID:
19018014
42.

Gas exchange in stable patients with moderate-to-severe lung disease from cystic fibrosis.

Soni R, Dobbin CJ, Milross MA, Young IH, Bye PP.

J Cyst Fibros. 2008 Jul;7(4):285-91.

43.

High prevalence of a class 1 integron-associated aadB gene cassette in Pseudomonas aeruginosa isolates from an Australian cystic fibrosis patient population.

Syrmis M, Bell S, Bye P, Coulter C, Harbour C, Iredell J, Kidd T, O'Carroll M, Rose B, Wainwright C, Sloots T, Nissen M.

Pathology. 2008 Aug;40(5):524-5. doi: 10.1080/00313020802197921. No abstract available.

PMID:
18604741
44.

Sleep-disordered breathing before and after lung transplantation.

Malouf MA, Milrose MA, Grunstein RR, Wong K, Prashant C, Jankelson DM, Aboyoun CL, Bye PT, Glanville AR.

J Heart Lung Transplant. 2008 May;27(5):540-6. doi: 10.1016/j.healun.2008.01.021. Erratum in: J Heart Lung Transplant. 2008 Oct;27(10):1190. Milross, Maree A [corrected to Milrose, Maree A].

PMID:
18442721
45.

Inhaled mannitol improves lung function in cystic fibrosis.

Jaques A, Daviskas E, Turton JA, McKay K, Cooper P, Stirling RG, Robertson CF, Bye PTP, LeSouëf PN, Shadbolt B, Anderson SD, Charlton B.

Chest. 2008 Jun;133(6):1388-1396. doi: 10.1378/chest.07-2294. Epub 2008 Mar 13.

PMID:
18339790
46.

Physiological responses to high intensity, constant-load arm exercise in COPD.

McKeough ZJ, Alison JA, Speers BA, Bye PT.

Respir Med. 2008 Mar;102(3):348-53. Epub 2007 Dec 11.

47.

Other mucoactive agents for cystic fibrosis.

Bye PT, Elkins MR.

Paediatr Respir Rev. 2007 Mar;8(1):30-9. Epub 2007 Mar 26. Review.

PMID:
17419976
48.

Phenotypic characterization of clonal and nonclonal Pseudomonas aeruginosa strains isolated from lungs of adults with cystic fibrosis.

Tingpej P, Smith L, Rose B, Zhu H, Conibear T, Al Nassafi K, Manos J, Elkins M, Bye P, Willcox M, Bell S, Wainwright C, Harbour C.

J Clin Microbiol. 2007 Jun;45(6):1697-704. Epub 2007 Mar 28.

49.

Glycosylation of sputum mucins is altered in cystic fibrosis patients.

Schulz BL, Sloane AJ, Robinson LJ, Prasad SS, Lindner RA, Robinson M, Bye PT, Nielson DW, Harry JL, Packer NH, Karlsson NG.

Glycobiology. 2007 Jul;17(7):698-712. Epub 2007 Mar 28.

PMID:
17392389
50.

Protease IV production in Pseudomonas aeruginosa from the lungs of adults with cystic fibrosis.

Smith L, Rose B, Tingpej P, Zhu H, Conibear T, Manos J, Bye P, Elkins M, Willcox M, Bell S, Wainwright C, Harbour C.

J Med Microbiol. 2006 Dec;55(Pt 12):1641-4.

PMID:
17108265

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