Professor Peter Bye

Clinical Professor
Medicine, Central Clinical School

Telephone +61 2 9515 7427
Fax +61 2 9515 8196

Map

Selected grants

2010

  • Novel interventions for the Diverse Population of Australians with Bronchiectasis; Bye P, Bell S, McCormack J, Elkins M, Marks G, Torzillo P, Harbour C, Wark P; National Health and Medical Research Council (NHMRC)/Project Grants.
  • Hypertonic saline for people with bronchiectasis; Bye P, Wark P, Elkins M, Harbour C, Bell S, McCormack J, Wark P, Torzillo P; Australian Respiratory Council/Harry Windsor Research Grants Scheme.
  • A randomised placebo-controlled trialof nebulised hypertonic saline in patients with Bronchiectasis; Bye P; DVC Research/Bridging Support Grant.

2008

  • Effect of exercise training on quality of life and exercise capacityin dust-related lung disease; Alison J, Corte P, McKeough Z, Bye P; Workers Compensation Dust Diseases Board of New South Wales/Research and Community Support Grants Scheme.
  • Effect of exercise training on quality of life and exercise capacity in people with dust-related lun; Alison J, McKeough Z, Corte P, Bye P; Workers Compensation Dust Diseases Board of New South Wales/Research Support.

2006

  • Sequencing of transmissible Pseudomonas aeruginosa from patients with cystic fibrosis; Harbour C, Rose B, Manos J, Arthur J, Bye P; Australian Cystic Fibrosis Research Trust/Research Support.

2005

  • Respiratory and Sleep Medicine; Jenkins C, Hensley M, Alison J, Britton W, Irwig L, Rogers N, Rose B, Marks G, Grunstein R, Bye P, Anderson S, King G, Berend N, Gibson P; National Health and Medical Research Council (NHMRC)/Centre of Clinical Research Excellence.
  • Viasys Impulse Oscillometer System with Pentium Device; Bye P, Elkins M, Alison J, McCarren B, Anderson S, Daviskas E; National Health and Medical Research Council (NHMRC)/Equipment Grants.

2003

  • Characterisation of P. aeruginosa isolates infecting CF patients: their capacity for transmission and antibiotic resistance; Harbour C, Rose B, Bye P, Robinson M, Bye P; Philip Bushell Foundation/Research Grant.
  • Evaluation of individual components of pulmonary rehabilitation in subjects with COPD; Thompson C, Alison J, Bye P; Community Health and Tuberculosis Australia (CHATA)/Harry Windsor Research Grant.

2002

  • Filancemeter (Tensiomat Semiautomatic Surface Tension Meter); Anderson S, Alison J, Daviskas L, Elkins M, Bye P, Robinson M; National Health and Medical Research Council (NHMRC)/Equipment Grants.
  • Evaluation of Lung Volume Reduction Surgery and Pulmonary Rehabilitation on Exercise Capacity, Upper; Spencer L, Barker-Whittle Z, Alison J, Bye P; Physiotherapy Research Foundation/Research Grant.
  • Evaluation of Lung Volume Reduction Surgery and Pulmonary Rehabilitation in Subjects with Chronic Ai; Barker-Whittle Z, Alison J, Bye P; Physiotherapists Registration Board (NSW Health)/Ian Collier Memorial Scolarship.
  • Assessment of physical therapies to improve secretion clearance in patients with cystic fibrosis; Robinson M, Bye P, Alison J, Eberl S; National Health and Medical Research Council (NHMRC)/Project Grants.

Selected publications

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Book Chapters

  • 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.

Journals

  • 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]
  • 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]
  • 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. The European Respiratory Journal, 41(5), 1091-1100. [More Information]
  • 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]
  • 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., 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]
  • 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]
  • 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]
  • 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]
  • 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]
  • 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]
  • 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.
  • 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]
  • 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]
  • 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.
  • 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. [More Information]
  • 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.
  • 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.
  • 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]
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.

Conferences

  • 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.
  • 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.
  • 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.
  • 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.

2014

  • 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]
  • 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. The European Respiratory Journal, 41(5), 1091-1100. [More Information]

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]

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]
  • 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]
  • 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.
  • 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. [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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.

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