Bourke SJ - Search Results

1

Ivacaftor and symptoms of extra-oesophageal reflux in patients with cystic fibrosis and G551D mutation.

Zeybel GL, Pearson JP, Krishnan A, Bourke SJ, Doe S, Anderson A, Faruqi S, Morice AH, Jones R, McDonnell M, Zeybel M, Dettmar PW, Brodlie M, Ward C. Zeybel GL, et al. Among authors: bourke sj. J Cyst Fibros. 2017 Jan;16(1):124-131. doi: 10.1016/j.jcf.2016.07.004. Epub 2016 Jul 27. J Cyst Fibros. 2017. PMID: 27475719 Free PMC article.

2

Risk factors for lung disease progression in children with cystic fibrosis.

Al Momani H, Perry A, Jones R, McDonnell M, Krishnan A, Robertson A, Griffin M, Rutherford R, Brodlie M, Pearson J, Bourke S, Ward C. Al Momani H, et al. Eur Respir J. 2018 Oct 4;52(4):1801492. doi: 10.1183/13993003.01492-2018. Print 2018 Oct. Eur Respir J. 2018. PMID: 30287494 Free article. No abstract available.

3

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

Shakir S, Echevarria C, Doe S, Brodlie M, Ward C, Bourke SJ. Shakir S, et al. Among authors: bourke sj. J Cyst Fibros. 2022 Sep;21(5):807-810. doi: 10.1016/j.jcf.2022.06.003. Epub 2022 Jun 16. J Cyst Fibros. 2022. PMID: 35718668 Free article.

4

Microbiological profiles of sputum and gastric juice aspirates in Cystic Fibrosis patients.

Al-Momani H, Perry A, Stewart CJ, Jones R, Krishnan A, Robertson AG, Bourke S, Doe S, Cummings SP, Anderson A, Forrest T, Griffin SM, Brodlie M, Pearson J, Ward C. Al-Momani H, et al. Sci Rep. 2016 Jun 1;6:26985. doi: 10.1038/srep26985. Sci Rep. 2016. PMID: 27245316 Free PMC article.

5

Nontuberculous mycobacteria in gastrostomy fed patients with cystic fibrosis.

Al-Momani H, Perry A, Jones R, Bourke S, Doe S, Perry J, Anderson A, Forrest T, Forrest I, Griffin M, Brodlie M, Pearson J, Ward C. Al-Momani H, et al. Sci Rep. 2017 Apr 24;7:46546. doi: 10.1038/srep46546. Sci Rep. 2017. PMID: 28436419 Free PMC article. Clinical Trial.

6

A novel culture medium for isolation of rapidly-growing mycobacteria from the sputum of patients with cystic fibrosis.

Preece CL, Perry A, Gray B, Kenna DT, Jones AL, Cummings SP, Robb A, Thomas MF, Brodlie M, O'Brien CJ, Bourke SJ, Perry JD. Preece CL, et al. Among authors: bourke sj. J Cyst Fibros. 2016 Mar;15(2):186-91. doi: 10.1016/j.jcf.2015.05.002. Epub 2015 May 20. J Cyst Fibros. 2016. PMID: 26002312 Free article.

7

Travelling abroad with cystic fibrosis: Assessment of risks and healthcare requirements.

Miller R, Blanch L, Lenaghan S, Anderson A, Doe S, Bourke SJ. Miller R, et al. Among authors: bourke sj. Respir Med. 2017 Apr;125:92-93. doi: 10.1016/j.rmed.2017.01.007. Epub 2017 Jan 24. Respir Med. 2017. PMID: 28188078 Free article.

8

Current characteristics, challenges and coping strategies of young people with cystic fibrosis as they transition to adulthood.

Askew K, Bamford J, Hudson N, Moratelli J, Miller R, Anderson A, Doe S, Bourke SJ. Askew K, et al. Among authors: bourke sj. Clin Med (Lond). 2017 Apr;17(2):121-125. doi: 10.7861/clinmedicine.17-2-121. Clin Med (Lond). 2017. PMID: 28365620 Free PMC article.

9

A service evaluation of an integrated model of palliative care of cystic fibrosis.

Bourke SJ, Booth Z, Doe S, Anderson A, Rice S, Gascoigne A, Quibell R. Bourke SJ, et al. Palliat Med. 2016 Jul;30(7):698-702. doi: 10.1177/0269216315626658. Epub 2016 Jan 26. Palliat Med. 2016. PMID: 26814212

10

Exposure to bile and gastric juice can impact the aerodigestive microbiome in people with cystic fibrosis.

Al-Momani H, Perry A, Nelson A, Stewart CJ, Jones R, Krishnan A, Robertson A, Bourke S, Doe S, Cummings S, Anderson A, Forrest T, Forrest I, Griffin M, Wilcox M, Brodlie M, Pearson J, Ward C. Al-Momani H, et al. Sci Rep. 2022 Jun 30;12(1):11114. doi: 10.1038/s41598-022-15375-4. Sci Rep. 2022. PMID: 35773410 Free PMC article.

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