McShane D - Search Results

1

Unresponsive asthma: Don't forget mediastinal masses.

Murray MJ, Nicholson JC, McShane D. Murray MJ, et al. Among authors: mcshane d. BMJ. 2008 Mar 8;336(7643):521-2. doi: 10.1136/bmj.39507.500336.80. BMJ. 2008. PMID: 18325941 Free PMC article. No abstract available.

2

Mediastinal masses masquerading as common respiratory conditions of childhood: a case series.

Saraswatula A, McShane D, Tideswell D, Burke GA, Williams DM, Nicholson JC, Murray MJ. Saraswatula A, et al. Among authors: mcshane d. Eur J Pediatr. 2009 Nov;168(11):1395-9. doi: 10.1007/s00431-009-0933-0. Epub 2009 Feb 11. Eur J Pediatr. 2009. PMID: 19205733

3

Congenital lung lesions: preoperative three-dimensional reconstructed CT scan as the definitive investigation and surgical management.

Saeed A, Kazmierski M, Khan A, McShane D, Gomez A, Aslam A. Saeed A, et al. Among authors: mcshane d. Eur J Pediatr Surg. 2013 Feb;23(1):53-6. doi: 10.1055/s-0033-1333890. Epub 2013 Feb 2. Eur J Pediatr Surg. 2013. PMID: 23378160

4

Inflammatory endobronchial polyps in childhood: clinical spectrum and possible link to mechanical ventilation.

McShane D, Nicholson AG, Goldstraw P, Ladas G, Travis WD, Ramanan R, Balfour-Lynn IM, Rosenthal M, Bush A. McShane D, et al. Pediatr Pulmonol. 2002 Jul;34(1):79-84. doi: 10.1002/ppul.10120. Pediatr Pulmonol. 2002. PMID: 12112802

5

Thirty-years of screening for cystic fibrosis in East Anglia.

Calvin J, Hogg SL, McShane D, McAuley SA, Iles R, Ross-Russell R, MacLean FM, Heeley ME, Heeley AF; Norfolk, Suffolk and Cambridgeshire Paediatric Cystic Fibrosis Network. Calvin J, et al. Among authors: mcshane d. Arch Dis Child. 2012 Dec;97(12):1043-7. doi: 10.1136/archdischild-2012-301968. Epub 2012 Oct 16. Arch Dis Child. 2012. PMID: 23076339

6

Multiresistant Pseudomonas aeruginosa in a pediatric cystic fibrosis center: natural history and implications for segregation.

Davies G, McShane D, Davies JC, Bush A. Davies G, et al. Among authors: mcshane d. Pediatr Pulmonol. 2003 Apr;35(4):253-6. doi: 10.1002/ppul.10262. Pediatr Pulmonol. 2003. PMID: 12629620

7

Normal nasal mucociliary clearance in CF children: evidence against a CFTR-related defect.

McShane D, Davies JC, Wodehouse T, Bush A, Geddes D, Alton EW. McShane D, et al. Eur Respir J. 2004 Jul;24(1):95-100. doi: 10.1183/09031936.04.00097503. Eur Respir J. 2004. PMID: 15293610 Free article.

8

Airway surface pH in subjects with cystic fibrosis.

McShane D, Davies JC, Davies MG, Bush A, Geddes DM, Alton EW. McShane D, et al. Eur Respir J. 2003 Jan;21(1):37-42. doi: 10.1183/09031936.03.00027603. Eur Respir J. 2003. PMID: 12570106 Free article.

9

Potential difference measurements in the lower airway of children with and without cystic fibrosis.

Davies JC, Davies M, McShane D, Smith S, Chadwick S, Jaffe A, Farley R, Collins L, Bush A, Scallon M, Pepper J, Geddes DM, Alton EW. Davies JC, et al. Among authors: mcshane d. Am J Respir Crit Care Med. 2005 May 1;171(9):1015-9. doi: 10.1164/rccm.200408-1116OC. Epub 2005 Jan 7. Am J Respir Crit Care Med. 2005. PMID: 15640364

10

Is deafness mutation screening required in cystic fibrosis patients?

Abusamra R, McShane D. Abusamra R, et al. Among authors: mcshane d. Paediatr Respir Rev. 2016 Aug;20 Suppl:24-6. doi: 10.1016/j.prrv.2016.06.010. Epub 2016 Jun 15. Paediatr Respir Rev. 2016. PMID: 27427311

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