Area of research
Pulmonary and Respiratory Medicine · Physiology
Research interest
Research interests include Cystic Fibrosis Research Advances, Chronic Obstructive Pulmonary Disease (COPD) Research, Neonatal Respiratory Health Research, and Asthma and respiratory diseases.
Detection of Bronchiolitis Obliterans Syndrome after Pediatric Hematopoietic Stem Cell Transplantation: An Official American Thoracic Society Clinical Practice Guideline
Phage Therapy of <i>Mycobacterium</i> Infections: Compassionate Use of Phages in 20 Patients With Drug-Resistant Mycobacterial Disease
Clinical significance and applications of oscillometry
Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for <i>F508del</i> and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study
Phase Transformation and Switching Behavior of Magnetron Plasma Sputtered Ge<sub>2</sub>Sb<sub>2</sub>Se<sub>4</sub>Te
Transient Tap Couplers for Wafer-Level Photonic Testing Based on Optical Phase Change Materials
Multiple breath washout: measuring early manifestations of lung pathology
Exposure to Stress and Air Pollution from Bushfires during Pregnancy: Could Epigenetic Changes Explain Effects on the Offspring?
Integrating the multiple breath washout test into international multicentre trials
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
Variability of lung clearance index in clinically stable cystic fibrosis lung disease in school age children
Effectiveness and response predictors of omalizumab in a severe allergic asthma population with a high prevalence of comorbidities: the Australian Xolair Registry
A Systematic Approach to Multiple Breath Nitrogen Washout Test Quality
Clinical characteristics of adult asthma associated with small airway dysfunction
Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report
Long-Term Outcomes of Children with Intermediate Sweat Chloride Values in Infancy
Lung clearance index in cystic fibrosis subjects treated for pulmonary exacerbations
Viral infections and asthma: an inflammatory interface?
Omalizumab in the management of steroid dependent Allergic Bronchopulmonary Aspergillosis (ABPA) complicating Cystic Fibrosis