Get started
Author

Barry S. Clements

Observed names: B CLEMENTS, B Clements, B S Clements, B. Clements, B. S. Clements, Barry CLEMENTS, Barry Clements, Barry S Clements, Clements, B.
Observed institutions: The Kids Research Institute Australia, The University of Western Australia, Princess Margaret Hospital for Children, Princess Margaret Cancer Centre, Royal Brompton Hospital, Princess Margaret Hospital, Princess Margaret Hospital, Perth Children's Hospital
ORCID: 0000-0002-2794-6563
Observed ORCID: 0000-0002-2794-6563
OpenAlex ID: A5058331959
Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR : a randomised, placebo-controlled phase 3 trial
2017 · Felix Ratjen, Christopher Hug, et al. · The Lancet Respiratory Medicine · 295
Pulmonary sequestration and related congenital bronchopulmonary-vascular malformations: nomenclature and classification based on anatomical and embryological considerations.
1987 · B S Clements, J O Warner · Thorax · 247
PDF
Acquisition and eradication ofP. aeruginosain young children with cystic fibrosis
2008 · T. A. Douglas, S. Brennan, et al. · European Respiratory Journal · 166
Efficacy and safety of elexacaftor plus tezacaftor plus ivacaftor versus tezacaftor plus ivacaftor in people with cystic fibrosis homozygous for F508del-CFTR: a 24-week, multicentre, randomised, double-blind, active-controlled, phase 3b trial
2021 · Sivagurunathan Sutharsan, Edward F McKone, et al. · The Lancet Respiratory Medicine · 148
Diagnosis of cystic fibrosis after newborn screening: The Australasian experience?twenty years and five million babies later: A consensus statement from the Australasian paediatric respiratory group
2005 · John Massie, Barry Clements, et al. · Pediatric Pulmonology · 80
PDF
Congenital bronchopulmonary vascular malformations: clinical application of a simple anatomical approach in 25 cases.
1987 · B S Clements, J O Warner, et al. · Thorax · 46
PDF
The effect of inhaled hypertonic saline on lung structure in children aged 3–6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial
2022 · Harm A W M Tiddens, Yuxin Chen, et al. · The Lancet Respiratory Medicine · 44
The Effect of Azithromycin on Structural Lung Disease in Infants with Cystic Fibrosis (COMBAT CF): A Phase 3, Randomised, Double-Blind, Placebo-Controlled Clinical Trial
2021 · Stephen M Stick, Alexia Foti, et al. · The Lancet Respiratory Medicine · 37
PDF
The crossover lung segment: congenital malformation associated with a variant of scimitar syndrome.
1987 · B S Clements, J O Warner · Thorax · 31
PDF
Changes in airway inflammation with pseudomonas eradication in early cystic fibrosis
2021 · Luke W Garratt, Oded Breuer, et al. · Journal of Cystic Fibrosis · 22
A new asthma spacer device to improve compliance in children: a pilot study
2004 · Gervase CHANEY, Barry CLEMENTS, et al. · Respirology · 16
Impact of Elexacaftor/Tezacaftor/Ivacaftor on Glucose Tolerance and Abnormal Glucose Metabolism: A Phase 3b, Open-Label Clinical Trial
2025 · Isabelle Durieu, Barry Clements, et al. · American Journal of Respiratory and Critical Care Medicine · 7
Role of Tris-CaEDTA as an adjuvant with nebulised tobramycin in cystic fibrosis patients with Pseudomonas aeruginosa lung infections: A randomised controlled trial
2020 · Ramaa Puvvadi, Helga Mikkelsen, et al. · Journal of Cystic Fibrosis · 7
PDF
Exercise-induced hypoxia secondary to an atrial septal defect and cor triatriatum dexter
2015 · Luke G. Eckersley, Barry Clements, et al. · Cardiology in the Young · 7
A phase I clinical trial assessing the safety, tolerability, and pharmacokinetics of inhaled ethanol in humans as a potential treatment for respiratory tract infections
2024 · David G. Hancock, William Ditcham, et al. · Frontiers in Medicine · 5
PDF
Jet versus vibrating mesh nebulizer for tobramycin aerosol in spontaneously breathing children with tracheostomies: A simulation study
2024 · Natalie V.E. Anderson, William G.F. Ditcham, et al. · Anaesthesia Critical Care & Pain Medicine · 2
Treatment with inhaled aerosolised ethanol reduces viral load and potentiates macrophage responses in an established influenza mouse model
2024 · David G. Hancock, Luke Berry, et al. · Experimental Lung Research · 1
PDF
Inhaled nebulised adrenaline delivery in children and adults: A simulation study
2025 · Natalie V. Anderson, William F. Ditcham, et al. · Anaesthesia Critical Care & Pain Medicine
529 Baseline results from the NEMO study: psychometric evaluation of the preschool cystic fibrosis questionnaire-revised in children with cystic fibrosis and caregivers in the United States and Australia
2025 · J. Chmiel, Q. Do, et al. · Journal of Cystic Fibrosis
WS05.03 A phase 3b study of the effects of elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) on glucose tolerance in people with cystic fibrosis (CF) and abnormal glucose metabolism
2023 · I. Durieu, B. Clements, et al. · Journal of Cystic Fibrosis
PDF
Guidelines for Weaning of Bronchodilator Therapy
2005 · LG Roddick, B Clements, et al. · Journal of Paediatrics and Child Health
Evidence that a new incentive spacer device encourages children to take their asthma medication
2001 · Chaney, G., Le Souef, Peter, et al. · UWA Profiles and Research Repository (UWA)
A Definitive Anatomical Classification of Pulmonary Sequestration: Review of 16 Cases
1985 · B S Clements, J O Warner, et al. · Pediatric Research
A Simple Infant Tracheostomy Protector
1985 · B CLEMENTS · The Lancet
Works count: 24
Citation count: 1,161
H-index: 11
I10-index: 11
Year
Topic
Type