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Cystic fibrosis pulmonary guidelines: airway clearance therapies.

Update on the epidemiology of gastro-oesophageal reflux disease: a systematic review

Murine liver repair via transient activation of regenerative pathways in hepatocytes using lipid nanoparticle-complexed nucleoside-modified mRNA

Telemedicine for healthcare: Capabilities, features, barriers, and applications

Systematic development of ionizable lipid nanoparticles for placental mRNA delivery using a design of experiments approach

European Cystic Fibrosis Society Standards of Care: Framework for the Cystic Fibrosis Centre

Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508delCFTR

Development and evaluation of a palliative care curriculum for cystic fibrosis healthcare providers

Cystic fibrosis

Lipid nanoparticles for mRNA delivery

Lipid nanoparticle chemistry determines how nucleoside base modifications alter mRNA delivery

Managing Cystic Fibrosis

Esophageal Eosinophilia In Children With Dysphagia

Usability in telemedicine systems—A literature survey

British Thoracic Society guidelines for the management of non-tuberculous mycobacterial pulmonary disease (NTM-PD)

Gastroesophageal reflux disease in children and adolescents in primary care

Antibiotic resistance of bacterial biofilms

Interlobar differences in bronchoalveolar lavage fluid from children with cystic fibrosis

Pediatric Gastroesophageal Reflux Clinical Practice Guidelines: Joint Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN)

Early intervention and prevention of lung disease in cystic fibrosis: a European consensus

Therapy of CF-Patients with Amitriptyline and Placebo - a Randomised, Double-Blind, Placebo-Controlled Phase IIb Multicenter, Cohort-Study

Airway Mucus Function and Dysfunction

Adoption of Digital Technologies in Health Care During the COVID-19 Pandemic: Systematic Review of Early Scientific Literature

Nebulized 3% Hypertonic Saline Solution Treatment in Ambulatory Children with Viral Bronchiolitis Decreases Symptoms

Nebulized hypertonic saline/salbutamol solution treatment in hospitalized children with mild to moderate bronchiolitis

Cystic fibrosis

Nebulised hypertonic saline for cystic fibrosis

Therapeutic efficacy in a hemophilia B model using a biosynthetic mRNA liver depot system

Semiquantitative Culture Analysis during Therapy for Mycobacterium avium Complex Lung Disease

Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis

A Feasibility Study of Urgent Implementation of Cystic Fibrosis Multidisciplinary Telemedicine Clinic in the Face of COVID-19 Pandemic: Single-Center Experience

Practical Guidelines: Lung Transplantation in Patients with Cystic Fibrosis

Chest physiotherapy compared to no chest physiotherapy for cystic fibrosis

SIDS and Other Sleep-Related Infant Deaths: Expansion of Recommendations for a Safe Infant Sleeping Environment

Esophageal Eosinophilia In Children With Dysphagia

Ionizable lipid nanoparticles deliver mRNA to pancreatic β cells via macrophage-mediated gene transfer

Pediatric Gastroesophageal Reflux Clinical Practice Guidelines

Clinical Practice Guideline: The Diagnosis, Management, and Prevention of Bronchiolitis

Ionizable lipid nanoparticles for in utero mRNA delivery

Exercise as medicine – evidence for prescribing exercise as therapy in 26 different chronic diseases

Management of Ingested Foreign Bodies in Children

Nebulised hypertonic saline for cystic fibrosis

Physiotherapy for cystic fibrosis in Australia: Knowledge and acceptance of the Consensus Statement recommendations

Chest physiotherapy in infants with cystic fibrosis: To tip or not? A five‐year study

Chest physiotherapy, gastro-oesophageal reflux, and arousal in infants with cystic fibrosis

Gastroesophageal Reflux (Symptomatic and Silent): A Potentially Significant Problem in Patients With Cystic Fibrosis Before and After Lung Transplantation

Inhaled hypertonic saline increases sputum expectoration in cystic fibrosis

Structure and Function of the Mucus Clearance System of the Lung

Pulmonary Rehabilitation Following Lung Transplantation

Gastro-oesophageal reflux in infants under 6 months with cystic fibrosis

The long term effect of inhaled hypertonic saline 6% in non-cystic fibrosis bronchiectasis

Benefits of music therapy as an adjunct to chest physiotherapy in infants and toddlers with cystic fibrosis

Postural drainage and gastro-oesophageal reflux in infants with cystic fibrosis

Feasibility and Acceptability of an Internet-Based Program to Promote Physical Activity in Adults With Cystic Fibrosis

S24.1. Chest physiotherapy for children with CF-birth to two years: issues to consider

Pain Impacts on Quality of Life and Interferes with Treatment in Adults with Cystic Fibrosis

Assessing Exercise Capacity Using Telehealth: A Feasibility Study in Adults With Cystic Fibrosis

Physiotherapy in infants and young children with cystic fibrosis: current practice and future developments.