Stephen J. Bourke

Newcastle Upon Tyne, ENG NE14LP, United Kingdom

Last Updated: 09/26/2026

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Found 27 publications

Creating a brand. Genesis, transformation and diffusion of Qurayyah Painted Ware.

Creating a brand. Genesis, transformation and diffusion of Qurayyah Painted Ware.

Journal: PloS one

Published: September 19, 2025

A descriptive study of patients diagnosed with cystic fibrosis or a CF-related disorder in adulthood.

A descriptive study of patients diagnosed with cystic fibrosis or a CF-related disorder in adulthood.

Journal: Clinical medicine (London, England)

Published: September 14, 2025

Corrigendum to "Optimising outcomes for adults with Cystic Fibrosis taking CFTR modulators by individualising care: Personalised data linkage to understand treatment optimisation (PLUTO), a novel clinical framework" [Respirat. Med. 239 (2025)].

Corrigendum to "Optimising outcomes for adults with Cystic Fibrosis taking CFTR modulators by individualising care: Personalised data linkage to understand treatment optimisation (PLUTO), a novel clinical framework" [Respirat. Med. 239 (2025)].

Journal: Respiratory medicine

Published: March 14, 2025

A descriptive cohort study of pregnancy and parenthood in women with cystic fibrosis.

A descriptive cohort study of pregnancy and parenthood in women with cystic fibrosis.

Journal: Clinical medicine (London, England)

Published: November 09, 2024

Optimising outcomes for adults with cystic fibrosis taking CFTR modulators by individualising care: Personalised data linkage to understand treatment optimisation (PLUTO), a novel clinical framework.

Optimising outcomes for adults with cystic fibrosis taking CFTR modulators by individualising care: Personalised data linkage to understand treatment optimisation (PLUTO), a novel clinical framework.

Journal: Respiratory medicine

Published: August 28, 2024

Recommendations for surveillance of pulmonary dysfunction among childhood, adolescent, and young adult cancer survivors: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group.

Recommendations for surveillance of pulmonary dysfunction among childhood, adolescent, and young adult cancer survivors: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group.

Journal: EClinicalMedicine

Published: December 21, 2023

Elexacaftor-Tezacaftor-Ivacaftor improve Gastro-Oesophageal reflux and Sinonasal symptoms in advanced cystic fibrosis.

Elexacaftor-Tezacaftor-Ivacaftor improve Gastro-Oesophageal reflux and Sinonasal symptoms in advanced cystic fibrosis.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: December 14, 2021

Decontamination Strategies Used for AFB Culture Significantly Reduce the Viability of Mycobacterium abscessus Complex in Sputum Samples from Patients with Cystic Fibrosis.

Decontamination Strategies Used for AFB Culture Significantly Reduce the Viability of Mycobacterium abscessus Complex in Sputum Samples from Patients with Cystic Fibrosis.

Journal: Microorganisms

Published: June 30, 2021

The impact of COVID-19 shielding on the wellbeing, mental health and treatment adherence of adults with cystic fibrosis.

The impact of COVID-19 shielding on the wellbeing, mental health and treatment adherence of adults with cystic fibrosis.

Journal: Future healthcare journal

Published: April 01, 2021

Oral cysteamine as an adjunct treatment in cystic fibrosis pulmonary exacerbations: An exploratory randomized clinical trial.

Oral cysteamine as an adjunct treatment in cystic fibrosis pulmonary exacerbations: An exploratory randomized clinical trial.

Journal: PloS one

Published: July 10, 2020

Krebs von den Lungen-6 (KL-6) is a pathophysiological biomarker of early-stage acute hypersensitivity pneumonitis among pigeon fanciers.

Krebs von den Lungen-6 (KL-6) is a pathophysiological biomarker of early-stage acute hypersensitivity pneumonitis among pigeon fanciers.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Published: May 07, 2020

Current status of fertility and family formation in men with cystic fibrosis.

Current status of fertility and family formation in men with cystic fibrosis.

Journal: Human fertility (Cambridge, England)

Published: August 31, 2019

Showing 1-12 of 27

Last Updated: 09/26/2026