scholarly journals The importance of data issues when comparing cystic fibrosis registry outcomes between countries: Are annual review FEV1 in the UK only collected when subjects are well?

2018 ◽  
Vol 24 (4) ◽  
pp. 745-751 ◽  
Author(s):  
Zhe Hui Hoo ◽  
Rachael Curley ◽  
Michael J. Campbell ◽  
Stephen J. Walters ◽  
Martin J. Wildman
Keyword(s):  
2016 ◽  
Vol 15 ◽  
pp. S112
Author(s):  
C. Sellar ◽  
R.M. Kaminski ◽  
D. Nazareth
Keyword(s):  

2019 ◽  
Vol 18 ◽  
pp. S81-S82
Author(s):  
E. McClenaghan ◽  
R. Cosgriff ◽  
M. Yip ◽  
S.C. Charman ◽  
A. Lee ◽  
...  
Keyword(s):  

2019 ◽  
Vol 13 (1) ◽  
pp. 39-46
Author(s):  
Jen Standen

In the UK over 10 000 people live with cystic fibrosis (CF), with 1-in-25 people being carriers of the disease. Multidisciplinary care is provided by tertiary care CF centres, with or without local secondary service shared care agreements. There are still, however, several reasons why CF sufferers or their families present to their GPs. This article aims to provide a brief overview of CF and its management. It also gives the information needed to guide patients about genetic testing and neonatal screening for the disease.


2014 ◽  
Vol 13 (2) ◽  
pp. 186-189 ◽  
Author(s):  
Sandra Chuang ◽  
Michael Doumit ◽  
Rebecca McDonald ◽  
Erika Hennessy ◽  
Tamarah Katz ◽  
...  

Author(s):  
Olga Archangelidi ◽  
Paul Cullinan ◽  
Nicholas J. Simmonds ◽  
Emmanouil Mentzakis ◽  
Daniel Peckham ◽  
...  

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