Adam Jaffe

Distress during airway sampling in children with cystic fibrosis.

Early glucose abnormalities in cystic fibrosis are preceded by poor weight gain.

The role of azithromycin in patients with cystic fibrosis.

Chemosensory function and food preferences of children with cystic fibrosis.

Noninvasive monitoring of glucose levels: is exhaled breath the answer?

Update of faecal markers of inflammation in children with cystic fibrosis.

Increased paediatric hospitalizations for empyema in Australia after introduction of the 7-valent pneumococcal conjugate vaccine.

Annual Review Clinic improves care in children with cystic fibrosis.

Childhood interstitial lung disease due to surfactant protein C deficiency: frequent use and costs of hospital services for a single case in Australia.

Fat-soluble vitamin deficiency in children and adolescents with cystic fibrosis.

Cannabis smoking and respiratory health: consideration of the literature.

Markers of inflammation in the breath in paediatric inflammatory bowel disease.

Primary ciliary dyskinesia: overlooked and undertreated in children.

A pilot study of inhaled dry-powder mannitol during cystic fibrosis-related pulmonary exacerbation.

Elevated fecal M2-pyruvate kinase in children with cystic fibrosis: a clue to the increased risk of intestinal malignancy in adulthood?

Markers of pancreatic function in the breath.

Rhinoviruses significantly affect day-to-day respiratory symptoms of children with asthma.

Use of the Lung Flute for sputum induction in children with cystic fibrosis: a pilot study.

Presentation of primary ciliary dyskinesia in children: 30 years' experience.

Intestinal inflammation and impact on growth in children with cystic fibrosis.

CareTrack Kids-part 1. Assessing the appropriateness of healthcare delivered to Australian children: study protocol for clinical indicator development.

CareTrack Kids-part 2. Assessing the appropriateness of the healthcare delivered to Australian children: study protocol for a retrospective medical record review.

CareTrack Kids-part 3. Adverse events in children's healthcare in Australia: study protocol for a retrospective medical record review.

Childhood interstitial lung disease: A systematic review.

Advances in the detection and management of cystic fibrosis related diabetes.

Fecal Human β-Defensin 2 in Children with Cystic Fibrosis: Is There a Diminished Intestinal Innate Immune Response?

Absence of back to school peaks in human rhinovirus detections and respiratory symptoms in a cohort of children with asthma.

Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis.

A population study of respiratory rehospitalisation in very preterm infants in the first 3 years of life.

Diagnosing cystic fibrosis-related diabetes: current methods and challenges.

Is there a role for stool metabolomics in cystic fibrosis?

Threat interpretation and parental influences for children with asthma and anxiety.

Attentional Bias in Children with Asthma with and without Anxiety Disorders.

Validation of a quantitative method to measure neural respiratory drive in children during sleep.

Association of rhinovirus with exacerbations in young children affected by cystic fibrosis: Preliminary data.

Age-dependent variation of fecal calprotectin in cystic fibrosis and healthy children.

Protective factors for social-emotional well-being of refugee children in the first three years of settlement in Australia.

Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: a decade's experience.

Anxiety in youth with asthma: A meta-analysis.

Age-related levels of fecal M2-pyruvate kinase in children with cystic fibrosis and healthy children 0 to 10years old.

Parent-child interactions in children with asthma and anxiety.

Increased doses of inhaled corticosteroids during home management of asthma flare-ups do not reduce the need for systemic steroids.

Rare disease registries: a call to action.

Association between respiratory syncytial viral disease and the subsequent risk of the first episode of severe asthma in different subgroups of high-risk Australian children: a whole-of-population-based cohort study.

Helping refugee children thrive: what we know and where to next.

Role of viral and bacterial pathogens in causing pneumonia among Western Australian children: a case-control study protocol.

Quality of Health Care for Children in Australia, 2012-2013.

Research priority setting in childhood chronic disease: a systematic review.

Research priorities for childhood chronic conditions: a workshop report.

The contribution of viruses and bacteria to community-acquired pneumonia in vaccinated children: a casecontrol study.

Association of Age at First Severe Respiratory Syncytial Virus Disease With Subsequent Risk of Severe Asthma: A Population-Based Cohort Study.

Human Primary Epithelial Cell Models: Promising Tools in the Era of Cystic Fibrosis Personalized Medicine.

Clinical indicators for common paediatric conditions: Processes, provenance and products of the CareTrack Kids study.

Quantitative assessment of nocturnal neural respiratory drive in children with and without obstructive sleep apnoea using surface EMG.

Combination of clinical symptoms and blood biomarkers can improve discrimination between bacterial or viral community-acquired pneumonia in children.

Assessing the quality of health care in the management of bronchiolitis in Australian children: a population-based sample survey.

Children's interstitial and diffuse lung disease.

Targeted Activation of Cystic Fibrosis Transmembrane Conductance Regulator.

Long-term morbidity of respiratory viral infections during chemotherapy in children with leukaemia.

Assessing the adherence to guidelines in the management of croup in Australian children: a population-based sample survey.

School students with chronic illness have unmet academic, social, and emotional school needs.

Facilitating engagement with school in students with chronic illness through positive education: A mixed-methods comparison study.

Gut Microbiota in Children With Cystic Fibrosis: A Taxonomic and Functional Dysbiosis.

Probiotics for people with cystic fibrosis.

Evaluating the Alimentary and Respiratory Tracts in Health and disease (EARTH) research programme: a protocol for prospective, longitudinal, controlled, observational studies in children with chronic disease at an Australian tertiary paediatric hospital.

Assessing the appropriateness of paediatric antibiotic overuse in Australian children: a population-based sample survey.

The intestinal virome in children with cystic fibrosis differs from healthy controls.

Nasopharyngeal density of respiratory viruses in childhood pneumonia in a highly vaccinated setting: findings from a case-control study.

Dispensing Practices of Fixed Dose Combination Controller Therapy for Asthma in Australian Children and Adolescents.

A systematic cochrane review of probiotics for people with cystic fibrosis.

A phospholipid-based formulation for the treatment of airway inflammation in chronic respiratory diseases.

Novel Antioxidant Therapy with the Immediate Precursor to Glutathione, γ-Glutamylcysteine (GGC), Ameliorates LPS-Induced Cellular Stress in In Vitro 3D-Differentiated Airway Model from Primary Cystic Fibrosis Human Bronchial Cells.

Epidemiology of COVID-19 infection in young children under five years: A systematic review and meta-analysis.

Significant functional differences in differentiated Conditionally Reprogrammed (CRC)- and Feeder-free Dual SMAD inhibited-expanded human nasal epithelial cells.

Assessing the impact of the 13 valent pneumococcal vaccine on childhood empyema in Australia.

Avatar acceptability: views from the Australian Cystic Fibrosis community on the use of personalised organoid technology to guide treatment decisions.

Community-based interventions for childhood asthma using comprehensive approaches: a systematic review and meta-analysis.

Cystic fibrosis-related diabetes and lung disease: an update.

Rate of use and effectiveness of oseltamivir in the treatment of influenza illness in high-risk populations: A systematic review and meta-analysis.

Treatment of Cystic Fibrosis: From Gene- to Cell-Based Therapies.

Surfactant protein disorders in childhood interstitial lung disease.

Antibiotic use for acute respiratory infections among under-5 children in Bangladesh: a population-based survey.

Assessment of Variation in Care Following Hospital Discharge for Children with Acute Asthma.

Parent-Collected Oropharyngeal Swabs in Cystic Fibrosis.