Doe SJ - Search Results

1

Aquagenic palmar wrinkling as a presenting feature of cystic fibrosis gene dysfunction.

Stewart LC, Doe SJ, Bourke SJ, Leech S. Stewart LC, et al. Among authors: doe sj. Clin Exp Dermatol. 2009 Dec;34(8):e647-9. doi: 10.1111/j.1365-2230.2009.03357.x. Epub 2009 Jun 22. Clin Exp Dermatol. 2009. PMID: 19548945

2

An integrated model of provision of palliative care to patients with cystic fibrosis.

Bourke SJ, Doe SJ, Gascoigne AD, Heslop K, Fields M, Reynolds D, Mannix K. Bourke SJ, et al. Among authors: doe sj. Palliat Med. 2009 Sep;23(6):512-7. doi: 10.1177/0269216309106312. Epub 2009 May 21. Palliat Med. 2009. PMID: 19460834

3

Provision of contraception services and advice for women with cystic fibrosis.

Gatiss S, Mansour D, Doe S, Bourke S. Gatiss S, et al. J Fam Plann Reprod Health Care. 2009 Jul;35(3):157-60. doi: 10.1783/147118909788708075. J Fam Plann Reprod Health Care. 2009. PMID: 19622205 Free article.

4

A new era in the treatment of cystic fibrosis.

Lane MA, Doe SJ. Lane MA, et al. Among authors: doe sj. Clin Med (Lond). 2014 Feb;14(1):76-8. doi: 10.7861/clinmedicine.14-1-76. Clin Med (Lond). 2014. PMID: 24532752 Free PMC article. No abstract available.

5

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. Among authors: doe s. Palliat Med. 2016 Jul;30(7):698-702. doi: 10.1177/0269216315626658. Epub 2016 Jan 26. Palliat Med. 2016. PMID: 26814212

6

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.

7

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: doe s. 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.

8

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: doe s. 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.

9

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: doe s. 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.

10

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.

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