Skip Navigation


QJM Advance Access originally published online on February 22, 2006
QJM 2006 99(3):196-197; doi:10.1093/qjmed/hcl018
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
99/3/196    most recent
hcl018v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Carter, K.
Right arrow Articles by Devereux, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Carter, K.
Right arrow Articles by Devereux, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Correspondence

Patients with bronchiectasis: look for specific causes

The first 10% of the full text of this article appears below.

Sir,

Over 90% of cases of cystic fibrosis are diagnosed in infancy or childhood, although older patients with phenotypically mild disease are occasionally discovered. We describe a patient with a long history of chronic suppurative lung disease, who was discovered to have cystic fibrosis in her seventh decade.

. . . [Full Text of this Article]

K. Carter, G.P. Currie and G. Devereux

Department of Respiratory Medicine Aberdeen Royal Infirmary Foresterhill Aberdeen

email: graeme.currie@nhs.net


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?