Publications for Peter Bye
Publications for Peter Bye
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. <a
href="http://dx.doi.org/10.1136/thoraxjnl-2014-2
06716">[More Information]</a>
2015
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.
<a
href="http://dx.doi.org/10.1016/j.jphys.2015.05.0
19">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1177/1479972315587
518">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1186/1471-2466-14-1
80">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.jcf.2013.10.003
">[More Information]</a>
2013
Dale, M., McKeough, Z., Munoz, P., Corte, P.,
Bye, P., Alison, J. (2013). Functional exercise
capacity and health-related
pseudomonas aeruginosa genotypes are common
in australian cystic fibrosis centres. European
Respiratory Journal, 41(5), 1091-1100. <a
href="http://dx.doi.org/10.1183/09031936.00060
512">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/S1836-9553(12)
70070-X">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1177/1479972312440
814">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.micpath.2012.0
3.011">[More Information]</a>
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. <a
href="http://dx.doi.org/10.5694/mja11.10719">[
More Information]</a>
pleural disease: an observational study. BMC
Pulmonary Medicine, 13(1), 1-7. <a
href="http://dx.doi.org/10.1186/1471-2466-13-1"
>[More Information]</a>
Lau, E., Cooper, W., Bye, P., Yan, K. (2011).
Difficult asthma and Churg-Strauss-like
syndrome: A cautionary tale. Respirology, 16(1),
180-181. <a
href="http://dx.doi.org/10.1111/j.1440-1843.201
0.01884.x">[More Information]</a>
Kidd, T., Ramsay, K., Hu, H., Marks, G.,
Wainwright, C., Bye, P., Elkins, M., Robinson,
P., Rose, B., Wilson, J., et al (2013). Shared
Dwyer, T., Alison, J., McKeough, Z., Daviskas,
E., Bye, P. (2011). Effects of Exercise on
Respiratory Flow and Sputum Properties in
quality of life in people with asbestos related
Publications for Peter Bye
Patients With Cystic Fibrosis. Chest, 139(4),
870-877. <a
href="http://dx.doi.org/10.1378/chest.10-1158">[
More Information]</a>
on arm exercise capacity in people with chronic
obstructive pulmonary disease: a randomised
controlled trial. APA Physiotherapy Conference
2011, NA.
Dale, M., McKeough, Z., Munoz, P., Corte, P.,
Bye, P., Alison, J. (2011). Exercise training
improves exercise capacity and
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. <a
href="http://dx.doi.org/10.1097/MCP.0b013e328
34b6af4">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1002/14651858.CD00
9385">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1002/cphy.c090012">[
More Information]</a>
Elkins, M., Bye, P. (2011). Mechanisms and
applications of hypertonic saline. Journal of the
Royal Society of Medicine, 104 suppl 1, s2-s5. <a
href="http://dx.doi.org/10.1258/jrsm.2011.s1110
1">[More Information]</a>
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.
<a
href="http://dx.doi.org/10.1111/j.1479-828X.201
0.01287.x">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1371/journal.pone.002
4526">[More Information]</a>
McKeough, Z., Bye, P., Alison, J. (2011). The
effect of endurance training and strength training
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. <a
href="http://dx.doi.org/10.1111/j.1440-1843.201
0.01792.x">[More Information]</a>
Lau, E., Moriarty, C., Ogle, R., Bye, P. (2010).
Pregnancy and Cystic Fibrosis. Paediatric
Respiratory Reviews, 11(2), 90-94. <a
href="http://dx.doi.org/10.1016/j.prrv.2010.01.00
8">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.rmed.2009.04.0
13">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1111/j.1574-6968.200
8.01472.x">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1128/JCM.00014-09"
>[More Information]</a>
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),
Publications for Peter Bye
761-768. <a
href="http://dx.doi.org/10.1164/rccm.200903-04
21OC">[More Information]</a>
021">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1378/chest.08-2948">[
More Information]</a>
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. <a
href="http://dx.doi.org/10.1099/jmm.0.2008/005
009-0">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.jcf.2009.05.005
">[More Information]</a>
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.
2008
2007
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.
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17392389">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=18604741">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1378/chest.07-2294">[
More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.healun.2008.01.
Bye, P., Elkins, M. (2007). Other mucoactive
agents for cystic fibrosis. Paediatric Respiratory
Reviews, 8(1), 30-39. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17419976">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17392437">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16421364">[More Information]</a>
McKeough, Z., Alison, J., Bye, P., Trenell, M.,
Publications for Peter Bye
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16516454">[More Information]</a>
Elkins, M., Bye, P. (2006). Inhaled hypertonic
saline as a therapy for cystic fibrosis. Current
Opinion in Pulmonary Medicine, 12(6), 445-452.
<a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17053496">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=17108265">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=15901828">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16207967">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16084254">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16264054">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16166615">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=16279152">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1002/ppul.20287">[M
ore Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=15831839">[More Information]</a>
2004
Vedam, H., Moriarty, C., Torzillo, P.,
McWilliam, D., Bye, P. (2004). Improved
Publications for Peter Bye
Outcomes Of Patients With Cystic Fibrosis
Admitted To The Intensive Care Unit. Journal of
Cystic Fibrosis, 3(1), 8-14. <a
href="http://dx.doi.org/10.1016/j.jcf.2003.12.003
">[More Information]</a>
(2003). Prevalence of haemoptysis in adults with
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.
2002
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. <a
href="http://dx.doi.org/10.1016/j.jcf.2004.07.002
">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.jhin.2004.01.00
3">[More Information]</a>
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. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=15068459">[More Information]</a>
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.
pulmonary atresia and ventricular septal defect,
and the role of mammary artery collateral
vessels. Heart, 89(8), 937-938.
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. <a
href="http://dx.doi.org/10.1002/ppul.10079">[M
ore Information]</a>
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,
Publications for Peter Bye
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.