2023

• Dwyer, T., Bye, P., Elkins, M., Dentice, R., Forbes, S., Cooper, P., Jaffe, A., Bishop, J., Middleton, P., Wark, P. (2023). Saline at lower tonicity in cystic fibrosis (SALTI-CF) trial comparing 0.9% versus 3% versus 6% nebulised saline. European Respiratory Journal, 62(1), 2100960. [More Information]

2021

• Aiyer, A., Visser, S., Bye, P., Britton, W., Whiteley, G., Glasbey, T., Kriel, F., Farrell, J., Ashish Kumar, T., Manos, J. (2021). Effect of n-acetylcysteine in combination with antibiotics on the biofilms of three cystic fibrosis pathogens of emerging importance. Antibiotics, 10(10), 1176. [More Information]

2020

• Dwyer, T., Griffin, B., Bye, P., Alison, J. (2020). Elicitation interview study to identify salient beliefs about exercise participation in adults with cystic fibrosis. Physiotherapy, 107, 286-291. [More Information]

2019

• Visser, S., Bye, P., Fox, G., Burr, L., Chang, A., Holmes-Liew, C., King, P., Middleton, P., Maguire, G., Smith, D., Britton, W., Morgan, L., et al (2019). Australian adults with bronchiectasis: The first report from the Australian Bronchiectasis Registry. Respiratory Medicine, 155, 97-103. [More Information]
• Dwyer, T., Daviskas, E., Zainuldin, M., Verschuer, J., Eberl, S., Bye, P., Alison, J. (2019). Effects of exercise and airway clearance (positive expiratory pressure) on mucus clearance in cystic fibrosis: a randomised crossover trial. European Respiratory Journal, 53(4), 1-11. [More Information]
• Visser, S., Bye, P., Fox, G., Burr, L., Chang, A., Holmes‑Liew, C., King, P., Middleton, P., Maguire, G., Smith, D., Britton, W., Morgan, L., et al (2019). Management of Australian Adults with Bronchiectasis in Tertiary Care: Evidence-Based or Access-Driven? Lung, 197(6), 803-810. [More Information]
• Milross, M., Piper, A., Dwyer, T., Wong, K., Bell, S., Bye, P. (2019). Non-invasive ventilation versus oxygen therapy in cystic fibrosis: A 12-month randomized trial. Respirology, 24(12), 1191-1197. [More Information]
• Milross, M., Piper, A., Dwyer, T., Bye, P. (2019). Non-invasive ventilation versus oxygen therapy in cystic fibrosis: Long-term effects - Reply. Respirology, 24(12), 1222-1223. [More Information]
• Dentice, R., Elkins, M., Verschuer, J., Eberl, S., Dwyer, G., Bye, P. (2019). Side lying during nebulisation can significantly improve apical deposition in healthy adults and adults with mild cystic fibrosis lung disease: A randomised crossover trial. BMC Pulmonary Medicine, 19(1), 1-7. [More Information]

2018

• Visser, S., Bye, P., Morgan, L. (2018). Management of bronchiectasis in adults. Medical Journal of Australia, 209(4), 177-183. [More Information]
• Dentice, R., Elkins, M., Dwyer, G., Bye, P. (2018). The use of an alternate side lying positioning strategy during inhalation therapy does not prolong nebulisation time in adults with Cystic Fibrosis: A randomised crossover trial. BMC Pulmonary Medicine, 18(1), 1-6. [More Information]
• Sivam, S., Dentice, R., Reddy, N., Moriarty, C., Yozghatlian, V., Mellis, C., Torzillo, P., Glanville, A., Gattas, D., Bye, P. (2018). Use of extracorporeal membrane oxygenation in cystic fibrosis in an Australian cystic fibrosis centre. Internal Medicine Journal, 48(3), 340-343. [More Information]

2017

• Daviskas, E., Sivam, S., Elkins, M., Dwyer, T., Dentice, R., Bye, P. (2017). Drug therapies that augment airway surface liquid. In Arata Azuma, Michael S. Schechter (Eds.), Treatment of Cystic Fibrosis and Other Rare Lung Diseases, (pp. 119-138). Cham: Springer International Publishing. [More Information]
• Dwyer, T., Zainuldin, M., Daviskas, E., Bye, P., Alison, J. (2017). Effects of treadmill exercise versus Flutter on respiratory flow and sputum properties in adults with cystic fibrosis: a randomised, controlled, cross-over trial. BMC Pulmonary Medicine, 17(1), 1-8. [More Information]

2016

• Dentice, R., Elkins, M., Middleton, P., Bishop, J., Wark, P., Dorahy, D., Harmer, C., Hu, H., Bye, P. (2016). A randomised trial of hypertonic saline during hospitalisation for exacerbation of cystic fibrosis. Thorax, 71(2), 141-147. [More Information]
• 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., Bye, P., et al (2016). Liver and lung transplantation in cystic fibrosis: an adult cystic fibrosis centre's experience. Internal Medicine Journal, 46(7), 852-854. [More Information]

2015

• Dale, M., McKeough, Z., Troosters, T., Bye, P., Alison, J. (2015). Exercise training to improve exercise capacity and quality oflife in people with non-malignant dust-related respiratorydiseases (Review). Cochrane Database of Systematic Reviews, 2015 (Issue 11. Art. No.: CD009385.), 1-48. [More Information]
• Dwyer, T., Robbins, L., Kelly, P., Piper, A., Bell, S., Bye, P. (2015). Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: a randomised trial. Journal of Physiotherapy, 61(3), 142-147. [More Information]
• Dale, M., McKeough, Z., Munoz, P., Corte, P., Bye, P., Alison, J. (2015). Physical activity in people with asbestos related pleural disease and dust-related interstitial lung disease: an observational study. Chronic Respiratory Disease, 12(4), 291-298. [More Information]

2014

• Dale, M., McKeough, Z., Munoz, P., Corte, P., Bye, P., Alison, J. (2014). Exercise training for asbestos-related and other dust-related respiratory diseases: a randomised controlled trial. BMC Pulmonary Medicine, 14(1), 1-9. [More Information]
• Sivam, S., Yozghatlian, V., Moriarty, C., Bye, P., Rees, D., Dentice, R. (2014). Spontaneous coronary artery dissection associated with coughing. Journal of Cystic Fibrosis, 13(2), 235-237. [More Information]

2013

• Dale, M., McKeough, Z., Munoz, P., Corte, P., Bye, P., Alison, J. (2013). Functional exercise capacity and health-related quality of life in people with asbestos related pleural disease: an observational study. BMC Pulmonary Medicine, 13(1), 1-7. [More Information]
• Harmer, C., Alnassafi, K., Hu, H., Elkins, M., Bye, P., Rose, B., Cordwell, S., Triccas, J., Harbour, C., Manos, J. (2013). Modulation of gene expression by Pseudomonas aeruginosa during chronic infection in the adult cystic fibrosis lung. Microbiology, 159(11), 2354-2363. [More Information]
• Kidd, T., Ramsay, K., Hu, H., Marks, G., Wainwright, C., Bye, P., Elkins, M., Robinson, P., Rose, B., Wilson, J., et al (2013). Shared pseudomonas aeruginosa genotypes are common in australian cystic fibrosis centres. European Respiratory Journal, 41(5), 1091-1100. [More Information]
• Alison, J., Bye, P., McKeough, Z. (2013). Upper limb strength and lung function as determinants of upper limb work capacity in chronic obstructive pulmonary disease. APA Conference 2013 'New Moves', Melbourne: Australian Physiotherapy Association.

2012

• Dentice, R., Elkins, M., Bye, P. (2012). Adults with cystic fibrosis prefer hypertonic saline before or during airway clearance techniques: a randomised crossover trial. Journal of Physiotherapy, 58(1), 33-40. [More Information]
• McKeough, Z., Bye, P., Alison, J. (2012). Arm exercise training in chronic obstructive pulmonary disease: A randomised controlled trial. Chronic Respiratory Disease, 9(3), 153-162. [More Information]
• Harmer, C., Triccas, J., Hu, H., Rose, B., Bye, P., Elkins, M., Manos, J. (2012). Pseudomonas aeruginosa strains from the chronically infected cystic fibrosis lung display increased invasiveness of A549 epithelial cells over time. Microbial Pathogenesis, 53(1), 37-43. [More Information]
• Alison, J., Bye, P., McKeough, Z. (2012). Upper limb strength and lung function as determinants of upper limb work capacity in COPD. European Respiratory Society Annual Congress 2012, United Kingdom: European Respiratory Society.

2011

• Bell, S., Bye, P., Cooper, P., Martin, A., McKay, K., Robinson, P., Ryan, G., Sims, G. (2011). Cystic fibrosis in Australia, 2009: results from a data registry. Medical Journal of Australia, 195(7), 396-400. [More Information]
• Lau, E., Cooper, W., Bye, P., Yan, K. (2011). Difficult asthma and Churg-Strauss-like syndrome: A cautionary tale. Respirology, 16(1), 180-181. [More Information]
• Dwyer, T., Alison, J., McKeough, Z., Daviskas, E., Bye, P. (2011). Effects of Exercise on Respiratory Flow and Sputum Properties in Patients With Cystic Fibrosis. Chest, 139(4), 870-877. [More Information]
• Dale, M., McKeough, Z., Munoz, P., Corte, P., Bye, P., Alison, J. (2011). Exercise training improves exercise capacity and quality of life in people with dust-related respiratory diseases: a randomised controlled trial. APA Physiotherapy Conference 2011, NA.
• Dale, M., McKeough, Z., Troosters, T., Bye, P., Alison, J. (2011). Exercise training to improve exercise capacity and quality of life in people with non-malignant dust-related respiratory diseases (Protocol). Cochrane Database of Systematic Reviews, (10), CD009385-1-CD009385-8. [More Information]
• Young, I., Bye, P. (2011). Gas Exchange in Disease: Asthma, Chronic Obstructive Pulmonary Disease, Cystic Fibrosis, and Interstitial Lung Disease. Comprehensive Physiology, 1(2), 663-697. [More Information]
• Elkins, M., Bye, P. (2011). Mechanisms and applications of hypertonic saline. Journal of the Royal Society of Medicine, 104 suppl 1, s2-s5. [More Information]
• Bye, P., Lau, E., Elkins, M. (2011). Pharmacological airway clearance strategies in bronchiectasis. European Respiratory Monograph, , 239-247.
• Lau, E., Barnes, D., Moriarty, C., Ogle, R., Dentice, R., Civitico, J., Avedello, A., Torzillo, P., Bye, P. (2011). Pregnancy outcomes in the current era of cystic fibrosis care: A 15-year experience. Australian and New Zealand Journal of Obstetrics and Gynaecology, 51(3), 220-224. [More Information]
• Naughton, S., Parker, D., Seemann, T., Thomas, T., Turnbull, L., Rose, B., Bye, P., Cordwell, S., Whitchurch, C., Manos, J. (2011). Pseudomonas aeruginosa AES-1 Exhibits Increased Virulence Gene Expression during Chronic Infection of Cystic Fibrosis Lung. PloS One, 6(9), e24526-1-e24526-8. [More Information]
• McKeough, Z., Bye, P., Alison, J. (2011). The effect of endurance training and strength training on arm exercise capacity in people with chronic obstructive pulmonary disease: a randomised controlled trial. APA Physiotherapy Conference 2011, NA.
• Dwyer, T., Elkins, M., Bye, P. (2011). The role of exercise in maintaining health in cystic fibrosis. Current Opinion in Pulmonary Medicine, 17(6), 455-460. [More Information]

2010

• Tingpej, P., Elkins, M., Rose, B., Hu, H., Moriarty, C., Manos, J., Barras, B., Bye, P., Harbour, C. (2010). Clinical profile of adult cystic fibrosis patients with frequent epidemic clones of Pseudomonas aeruginosa. Respirology, 15(6), 923-929. [More Information]
• Lau, E., Moriarty, C., Ogle, R., Bye, P. (2010). Pregnancy and Cystic Fibrosis. Paediatric Respiratory Reviews, 11(2), 90-94. [More Information]

2009

• Dwyer, T., Alison, J., McKeough, Z., Elkins, M., Bye, P. (2009). Evaluation of the SenseWear activity monitor during exercise in cystic fibrosis and in health. Respiratory Medicine, 103(10), 1511-1517. [More Information]
• Manos, J., Arthur, J., Rose, B., Bell, S., Tingpej, P., Hu, H., Webb, J., Kjelleberg, S., Gorrell, M., Bye, P., Harbour, C. (2009). Gene expression characteristics of a cystic fibrosis epidemic strain of Pseudomonas aeruginosa during biofilm and planktonic growth. FEMS Microbiology Letters, 292(1), 107-114. [More Information]
• Kidd, T., Ramsay, K., Hu, H., Bye, P., Elkins, M., Grimwood, K., Harbour, C., Marks, G., Nissen, M., Robinson, P., Rose, B., et al (2009). Low rates of Pseudomonas aeruginosa misidentification in isolates from cystic fibrosis patients. Journal of Clinical Microbiology, 47(5), 1503-1509. [More Information]
• Kidd, T., Marks, G., Bye, P., Wainwright, C., Robinson, P., Rose, B., Harbour, C., Bell, S. (2009). Multi-centre research in Australia: analysis of a recent National Health and Medical Research Council-funded project. Respirology, 14(7), 1051-1055. [More Information]
• Vandemheen, K., O'Connor, A., Bell, S., Freitag, A., Bye, P., Jeanneret, A., Berthiaume, Y., Brown, N., Wilcox, P., Middleton, P. (2009). Randomized Trial of a Decision Aid for Patients with Cystic Fibrosis Considering Lung Transplantation. American Journal of Respiratory and Critical Care Medicine, 180(8), 761-768. [More Information]
• Lau, E., Yozghatlian, V., Kosky, C., Moriarty, C., Dentice, R., Waugh, R., Torzillo, P., Bye, P. (2009). Recombinant activated factor VII for massive hemoptysis in patients with cystic fibrosis. Chest, 136(1), 277-281. [More Information]
• Sawyer, S., Farrant, B., Wilson, J., Ryan, G., O'Carroll, M., Bye, P., Bell, S. (2009). Sexual and reproductive health in men with cystic fibrosis: Consistent preferences, inconsistent practices. Journal of Cystic Fibrosis, 8(4), 264-269. [More Information]

2008

• Dwyer, T., Alison, J., McKeough, Z., Elkins, M., Bye, P. (2008). Evaluation of the SenseWear Pro3 Armband to measure energy expenditure during treadmill walking in CF and healthy age-matched control subjects. Pediatric Pulmonology, 43(supplement 31), p386: A514-p386.
• Dwyer, T., Alison, J., McKeough, Z., Daviskas, E., Bye, P. (2008). Exercise aids airway clearance by increasing respiratory flow rates and decreasing mucus viscoelasticity in CF. Pediatric Pulmonology, 43(Supplement31), p386: A513-p386.
• Syrmis, M., Bell, S., Bye, P., Coulter, C., Harbour, C., Iredell, J., Kidd, T., O'Carroll, M., Rose, B., Wainwright, C., Nissen, M., et al (2008). High prevalence of a class 1 integron-associated aadB gene cassette in Pseudomonas aeruginosa isolates from an Australian cystic fibrosis patient population. Pathology, 40(5), 524-525. [More Information]
• Jacques, A., Daviskas, E., Turton, J., McKay, K., Cooper, P., Stirling, R., Robertson, C., Bye, P., LeSouëf, P., Shadbolt, B., et al (2008). Inhaled Mannitol Improves Lung Function in Cystic Fibrosis. Chest, 133(6), 1388-1396. [More Information]
• McKeough, Z., Alison, J., Speers, B., Bye, P. (2008). Physiological responses to high intensity, constant-load arm exercise in COPD. Respiratory Medicine, 102, 348-353. [More Information]
• Malouf, M., Milross, M., Grunstein, R., Wong, K., Prashant, C., Jankelson, D., Aboyoun, C., Bye, P., Glanville, A. (2008). Sleep-disordered breathing before and after lung transplantation. Journal Of Heart And Lung Transplantation, 27(5), 540-546. [More Information]
• Manos, J., Arthur, J., Rose, B., Tingpej, P., Fung, C., Curtis, M., Webb, J., Hu, H., Kjelleberg, S., Gorrell, M., Bye, P., Harbour, C. (2008). Transcriptome analyses and biofilm-forming characteristics of a clonal Pseudomonas aeruginosa from the cystic fibrosis lung. Journal of Medical Microbiology, 57(12), 1454-1465. [More Information]
• Dwyer, T., Alison, J., McKeough, Z., Daviskas, E., Bye, P. (2008). Within-subject variability of mucus viscoelasticity and solids content of spontaneously expectorated sputum is higher in samples collected on different days than in samples collected on the same day for CF adults. Pediatric Pulmonology, 43(supplement 31), p242-A121.

2007

• Schulz, B., Sloane, A., Robinson, L., Prasad, S., Lindner, R., Robinson, M., Bye, P., Nielson, D., Harry, J., Packer, N., et al (2007). Glycosylation of sputum mucins is altered in cystic fibrosis patients. Glycobiology, 17(7), 698-712. [More Information]
• Bye, P., Elkins, M. (2007). Other mucoactive agents for cystic fibrosis. Paediatric Respiratory Reviews, 8(1), 30-39. [More Information]
• Tingpej, P., Smith, L., Rose, B., Zhu, H., Conibear, T., Al Nassafi, K., Manos, J., Elkins, M., Bye, P., Willcox, M., Harbour, C., et al (2007). Phenotypic characterization of clonal and nonclonal Pseudomonas aeruginosa strains isolated from lungs of adults with cystic fibrosis. Journal of Clinical Microbiology, 45(6), 1697-1704. [More Information]

2006

• Elkins, M., Robinson, M., Rose, B., Harbour, C., Moriarty, C., Marks, G., Belousova, E., Xuan, W., Bye, P., National Hypertonic Saline in Cystic Fibrosis (NHSCF) Study Group. (2006). A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. New England Journal of Medicine, 354(3), 229-240. [More Information]
• McKeough, Z., Alison, J., Bye, P., Trenell, M., Sachinwalla, T., Thompson, C., Kemp, G. (2006). Exercise capacity and quadriceps muscle metabolism following training in subjects with COPD. Respiratory Medicine, 100(10), 1817-1825. [More Information]
• Elkins, M., Bye, P. (2006). Inhaled hypertonic saline as a therapy for cystic fibrosis. Current Opinion in Pulmonary Medicine, 12(6), 445-452. [More Information]
• Smith, L., Rose, B., Tingpej, P., Zhu, H., Conibear, T., Manos, J., Bye, P., Elkins, M., Willcox, M., Bell, S., Harbour, C., et al (2006). Protease IV production in Pseudomonas aeruginosa from the lungs of adults with cystic fibrosis. Journal of Medical Microbiology, 55(Pt 12), 1641-1644. [More Information]

2005

• Pedersen, S., Sloane, A., Prasad, S., Sebastian, L., Lindner, R., Robinson, M., Hsu, M., Bye, P., Weinberger, R., Harry, J. (2005). An immunoproteomic approach for identification of clinical biomarkers for monitoring disease: application to cystic fibrosis. Molecular and Cellular Proteomics, 4(8), 1052-1060. [More Information]
• Hill, D., Rose, B., Pajkos, A., Robinson, M., Bye, P., Bell, S., Elkins, M., Thompson, B., Macleod, C., Aaron, S., Harbour, C. (2005). Antibiotic susceptibilities of Pseudomonas aeruginosa isolates derived from patients with cystic fibrosis under aerobic, anaerobic, and biofilm conditions. Journal of Clinical Microbiology, 43(10), 5085-5090. [More Information]
• Aaron, S., Vandemheen, K., Ferris, W., Fergusson, D., Tullis, E., Haase, D., Berthiaume, Y., Brown, N., Wilcox, P., Bye, P., Rose, B., Harbour, C., et al (2005). Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: a randomised, double-blind, controlled clinical trial. The Lancet, 366(9484), 463-471. [More Information]
• Elkins, M., Lane, T., Goldberg, H., Pagliuso, J., Garske, L., Hector, E., Marchetto, L., Alison, J., Bye, P. (2005). Effect of airway clearance techniques on the efficacy of the sputum induction procedure. European Respiratory Journal, 26(5), 904-908. [More Information]
• Punch, G., Syrmis, M., Rose, B., Harbour, C., Bye, P., Nissen, M., Elkins, M., Sloots, T. (2005). Method for detection of respiratory viruses in the sputa of patients with cystic fibrosis. European Journal of Clinical Microbiology and Infectious Diseases, 24(1), 54-57. [More Information]
• Bye, P., Elkins, M. (2005). Mucociliary Clearance and Cystic Fibrosis. In Q. Hamid, J. Shannon, J. Martin (Eds.), Physiologic Basis of Respiratory Disease, (pp. 417-428). United States of America: BC Decker Inc.
• Bye, P., Sloane, A., Lindner, R., Prasad, S., Sebastian, L., Pedersen, S., Robinson, M., Nielson, D., Harry, J. (2005). Proteomic analysis of sputum from adults and children with cystic fibrosis and from control subjects. American Journal of Respiratory and Critical Care Medicine, 172(11), 1416-26. [More Information]
• McKeough, Z., Alison, J., Bayfield, M., Bye, P. (2005). Supported and unsupported arm exercise capacity following lung volume reduction surgery: a pilot study. Chronic Respiratory Disease, 2(2), 59-65. [More Information]
• Elkins, M., Alison, J., Bye, P. (2005). The effect of body position on maximal expiratory pressure and flow in adults with cystic fibrosis. Pediatric Pulmonology, 40(5), 385-391. [More Information]
• Dobbin, C., Bartlett, D., Melehan, K., Grunstein, R., Bye, P. (2005). The Effect of Infective Exacerbations on Sleep and Neurobehavioral Function in Cystic Fibrosis. American Journal of Respiratory and Critical Care Medicine, 172(1), 99-104. [More Information]

2004

• Vedam, H., Moriarty, C., Torzillo, P., McWilliam, D., Bye, P. (2004). Improved Outcomes Of Patients With Cystic Fibrosis Admitted To The Intensive Care Unit. Journal of Cystic Fibrosis, 3(1), 8-14. [More Information]
• McKeough, Z., Alison, J., Bayfield, M., Bye, P. (2004). Reduction in resting energy expenditure following lung volume reduction surgery in subjects with Chronic Obstructive Pulmonary Disease. Chronic Respiratory Disease, 1(4), 197-202. [More Information]
• Dobbin, C., Milross, M., Piper, A., Sullivan, C., Grunstein, R., Bye, P. (2004). Sequential Use Of Oxygen And Bi-Level Ventilation For Respiratory Failure In Cystic Fibrosis. Journal of Cystic Fibrosis, 3(4), 237-242. [More Information]
• Milross, M., Piper, A., Dobbin, C., Bye, P., Grunstein, R. (2004). Sleep Disordered Breathing In Cystic Fibrosis. Sleep Medicine Reviews, 8(4), 295-308. [More Information]
• Dobbin, C., Maley, M., Harkness, J., Benn, R., Malouf, M., Glanville, A., Bye, P. (2004). The Impact Of Pan-Resistant Bacterial Pathogens On Survival After Lung Transplantation In Cystic Fibrosis: Results From A Single Large Referral Centre. Journal of Hospital Infection, 56, 277-82. [More Information]
• Wells, J., Kosky, C., Scolyer, R., Lee, S., Bye, P., Young, G., Davies, L. (2004). Unusual Case Of Subcutaneous Panniculitis-Like T-Cell Lymphoma. Australasian Journal of Dermatology, 45(2), 114-118. [More Information]

2003

• McKeough, Z., Alison, J., Bye, P. (2003). Arm exercise capacity and dyspnea ratings in subjects with chronic obstructive pulmonary disease. Journal of Cardiopulmonary Rehabilitation, 23, 218-225. [More Information]
• McKeough, Z., Alison, J., Bye, P. (2003). Arm positioning alters lung volumes in subjects with COPD and healthy subjects. Australian Journal of Physiotherapy, 49(2), 133-137. [More Information]
• Armstrong, D., Bell, S., Robinson, M., Bye, P., Rose, B., Harbour, C., Lee, C., Service, H., Nissen, M., Syrmis, M., et al (2003). Evidence for spread of a clonal strain of Pseudomonas aeruginosa among cystic fibrosis clinics. Journal of Clinical Microbiology, 41(5), 2266-2267. [More Information]
• Greaves, K., Bye, P., Parker, G., Celermajer, D. (2003). Prevalence of haemoptysis in adults with pulmonary atresia and ventricular septal defect, and the role of mammary artery collateral vessels. Heart, 89(8), 937-938.

2002

• Barker-Whittle, Z., Alison, J., Bye, P. (2002). Arm exercise capacity four to eight months after lung volume reduction surgery in subjects with chronic obstructive pulmonary disease. From Cell to Society 3, Sydney: The College of Health Sciences.
• Barker-Whittle, Z., Alison, J., Bye, P. (2002). Comparison of the cardiorespiratory responses between leg exercise, supported arm exercise and unsupported arm exercise in severe chronic airflow limitation (CAL). VIIth International Physiotherapy Congress, Sydney: Australian Physiotherapy Association.
• Soni, R., Marks, G., Henry, D., Robinson, M., Moriarty, C., Parsons, S., Taylor, P., Mahenthiralingam, E., Speert, D., Bye, P. (2002). Effect of Burkholderia cepacia infection in the clinical course of patients with cystic fibrosis: a pilot study in a Sydney clinic. Respirology, 7(3), 241-245. [More Information]
• Anthony, M., Rose, B., Pegler, M., Elkins, M., Service, H., Thamotharampillai, K., Watson, J., Robinson, M., Bye, P., Merlino, J., Harbour, C. (2002). Genetic analysis of Pseudomonas aeruginosa isolates from the sputa of adult Australian cystic fibrosis patients. Journal of Clinical Microbiology, 40(8), 2772-2778. [More Information]
• Robinson, M., Bye, P. (2002). Mucociliary clearance in cystic fibrosis. Pediatric Pulmonology, 33(4), 293-306. [More Information]
• Milross, M., Piper, A., Norman, M., Willson, G., Grunstein, R., Sullivan, C., Bye, P. (2002). Night-to-night variability in sleep in cystic fibrosis. Sleep Medicine, 3(3), 213-219. [More Information]
• Daviskas, E., Robinson, M., Anderson, S., Bye, P. (2002). Osmotic stimuli increase clearance of mucus in patients with mucociliary dysfunction. Journal of Aerosol Medicine, 15(3), 331-341. [More Information]
• Milross, M., Piper, A., Norman, M., Dobbin, C., Grunstein, R., Sullivan, C., Bye, P. (2002). Subjective sleep quality in cystic fibrosis. Sleep Medicine, 3(3), 205-212. [More Information]
• Alison, J., Bye, P., Elkins,, M., Eberl, S., Daviskas, E., Constable, C., Robinson, M. (2002). Three-dimensional quantification of mucociliary clearance in healthy subjects. VIIth International Physiotherapy Congress., Sydney: Australian Physiotherapy Association.

2001

• Milross, M., Norman, M., Willson, G., Grunstein, R., Sullivan, C., Bye, P., Piper, A., Becker,, H. (2001). Low-flow oxygen and bilevel ventilatory support: effects on ventilation during sleep in cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 163, 129-134.
• Milross, M., Norman, M., Willson, G., Grunstein, R., Sullivan, C., Bye, P., Piper, A. (2001). Predicting sleep-disordered breathing in patients with cystic fibrosis. Chest, 120, 1239-1245. [More Information]