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94 Comparison of biofilm characteristics of Pseudomonas aeruginosa isolated from people with cystic fibrosis (CF) and the natural environment

Journal of cystic fibrosis, 2017-06, Vol.16, p.S88-S89

2017

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74 Emergence of a shared Pseudomonas aeruginosa strain within an adult cystic fibrosis centre

Journal of cystic fibrosis, 2016-06, Vol.15, p.S70-S70

2016

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WS14.4 Pseudomonas aeruginosa (Pa) population fluctuation in cystic fibrosis (CF) pulmonary exacerbations – a battle of the strains?

Journal of cystic fibrosis, 2016-06, Vol.15, p.S23-S23

2016

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107 Time trends in clinical indicators for cystic fibrosis (CF) patients at transition to adult care

Journal of cystic fibrosis, 2014-06, Vol.13, p.S73-S73

2014

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IPD1.02 Tropical Australia is a potential reservoir of non-tuberculous mycobacteria (NTM) in cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S55-S55

2017

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Clonal strains of Pseudomonas aeruginosa in paediatric and adult cystic fibrosis units

The European respiratory journal, 2004-07, Vol.24 (1), p.101-106

2004

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WS01.6 Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa sub-lineage in cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S2-S2

2016

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250 Patient-reported outcomes among patients (pts) with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor (IVA) compared with those homozygous for the F508del-CFTR mutation

Journal of cystic fibrosis, 2016-06, Vol.15, p.S115-S115

2016

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WS13.6 GLPG1837 in subjects with cystic fibrosis (CF) and the G551D mutation: results from a phase II study (SAPHIRA1)

Journal of cystic fibrosis, 2017-06, Vol.16, p.S24-S25

2017

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143 The social network in cystic fibrosis centre care and the risk of shared Pseudomonas aeruginosa strain infection

Journal of cystic fibrosis, 2013-06, Vol.12, p.S85-S85

2013

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WS21.5 A comparative study of motility and biofilm production in cystic fibrosis (CF) and environmental Pseudomonas aeruginosa (Pa) isolates

Journal of cystic fibrosis, 2014-06, Vol.13, p.S42-S42

2014

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100 (More) viable cough aerosols from individuals with cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S76-S77

2016

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Frequency Sensitivity and Electromechanical Propagation Simulation Study in Large Power Systems

IEEE transactions on circuits and systems. 1, Fundamental theory and applications, 2007-08, Vol.54 (8), p.1819-1828

2007

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350 A retrospective study of cancer in Australian and New Zealand cystic fibrosis (CF) patients

Journal of cystic fibrosis, 2012-06, Vol.11, p.S146-S146

2012

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230 Review of bowel preparation in adults with cystic fibrosis requiring colonoscopy

Journal of cystic fibrosis, 2012-06, Vol.11, p.S115-S115

2012

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Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation

Journal of cystic fibrosis, 2013-05, Vol.12 (3), p.303-304

2013

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Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review

The Journal of hospital infection, 2019-10, Vol.103 (2), p.175-184

2019

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Patterns of Uterine Cellular Proliferation and Apoptosis in the Implantation Site of the Rat During Pregnancy

Placenta (Eastbourne), 2004-07, Vol.25 (6), p.538-547

2004

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WS17.6 Phase 3 trial of inhaled levofloxacin (Aeroquin™, MP-376, APT-1026) vs. tobramycin inhalation solution (TIS) in intensively treated CF patients over 6 months

Journal of cystic fibrosis, 2013-06, Vol.12, p.S35-S35

2013

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WS7.4 Lumacaftor, an investigational CFTR corrector, in combination with ivacaftor, a CFTR potentiator, in CF patients with the F508del-CFTR mutation: Phase 2 interim analysis

Journal of cystic fibrosis, 2013-06, Vol.12, p.S14-S14

2013

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110 A decade of Burkholderia cepacia complex (Bcc) infection in Queensland, Australia: 2001 to 2010

Journal of cystic fibrosis, 2012-06, Vol.11, p.S84-S84

2012

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129 Comparison of clinical and environmental Pseudomonas aeruginosa: evidence for recombination

Journal of cystic fibrosis, 2011, Vol.10, p.S33-S33

2011

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412: Antibiotic Desensitisation in Cystic Fibrosis Patients with a History of Hypersensitivity Undergoing Lung Transplantation Is Not Mandatory

The Journal of heart and lung transplantation, 2010-02, Vol.29 (2), p.S136-S136

2010

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201: The Outcome of Conventional Lung Volume Reduction Surgery Significantly Exceeds That of Lung Transplantation for Emphysema

The Journal of heart and lung transplantation, 2009-02, Vol.28 (2), p.S136-S136

2009

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WS18.4 Heterogeneity of shared Pseudomonas aeruginosa (Pa) strains between Australian states and centres in cystic fibrosis (CF)

Journal of cystic fibrosis, 2012-06, Vol.11, p.S41-S41

2012

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94 Comparison of biofilm characteristics of Pseudomonas aeruginosa isolated from people with cystic fibrosis (CF) and the natural environment

74 Emergence of a shared Pseudomonas aeruginosa strain within an adult cystic fibrosis centre

WS14.4 Pseudomonas aeruginosa (Pa) population fluctuation in cystic fibrosis (CF) pulmonary exacerbations – a battle of the strains?

107 Time trends in clinical indicators for cystic fibrosis (CF) patients at transition to adult care

IPD1.02 Tropical Australia is a potential reservoir of non-tuberculous mycobacteria (NTM) in cystic fibrosis

Clonal strains of Pseudomonas aeruginosa in paediatric and adult cystic fibrosis units

WS01.6 Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa sub-lineage in cystic fibrosis

250 Patient-reported outcomes among patients (pts) with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor (IVA) compared with those homozygous for the F508del-CFTR mutation

WS13.6 GLPG1837 in subjects with cystic fibrosis (CF) and the G551D mutation: results from a phase II study (SAPHIRA1)

143 The social network in cystic fibrosis centre care and the risk of shared Pseudomonas aeruginosa strain infection

WS21.5 A comparative study of motility and biofilm production in cystic fibrosis (CF) and environmental Pseudomonas aeruginosa (Pa) isolates

100 (More) viable cough aerosols from individuals with cystic fibrosis

Frequency Sensitivity and Electromechanical Propagation Simulation Study in Large Power Systems

350 A retrospective study of cancer in Australian and New Zealand cystic fibrosis (CF) patients

230 Review of bowel preparation in adults with cystic fibrosis requiring colonoscopy

Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation

Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review

Patterns of Uterine Cellular Proliferation and Apoptosis in the Implantation Site of the Rat During Pregnancy

WS17.6 Phase 3 trial of inhaled levofloxacin (Aeroquin™, MP-376, APT-1026) vs. tobramycin inhalation solution (TIS) in intensively treated CF patients over 6 months

WS7.4 Lumacaftor, an investigational CFTR corrector, in combination with ivacaftor, a CFTR potentiator, in CF patients with the F508del-CFTR mutation: Phase 2 interim analysis

110 A decade of Burkholderia cepacia complex (Bcc) infection in Queensland, Australia: 2001 to 2010

129 Comparison of clinical and environmental Pseudomonas aeruginosa: evidence for recombination

412: Antibiotic Desensitisation in Cystic Fibrosis Patients with a History of Hypersensitivity Undergoing Lung Transplantation Is Not Mandatory

201: The Outcome of Conventional Lung Volume Reduction Surgery Significantly Exceeds That of Lung Transplantation for Emphysema

WS18.4 Heterogeneity of shared Pseudomonas aeruginosa (Pa) strains between Australian states and centres in cystic fibrosis (CF)

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