Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 44 entries
Sorted by: Best Match Show Resources per page
[Pulmonary manifestations of mucoviscidosis in children].

Le Poumon et le coeur

Gilly R.
PMID: 5958992
Poumon Coeur. 1966;22(8):945-59.

No abstract available.

Respiratory complications of cystic fibrosis. Prevention.

Minnesota medicine

Warwick WJ.
PMID: 5824171
Minn Med. 1969 Sep;52(9):1567-9.

No abstract available.

[Mucoviscidosis: prognostic factors in 1991].

Pediatrie

Lenoir G, Silly C.
PMID: 1319038
Pediatrie. 1992;47(3):169-73.

No abstract available.

Question 10: Could the Burden of Care with Cystic Fibrosis Impact on Educational Outcomes?.

Paediatric respiratory reviews

Hanxhiu A, McKay K, Singh-Grewal D, Fitzgerald DA.
PMID: 27427312
Paediatr Respir Rev. 2017 Jun;23:56-60. doi: 10.1016/j.prrv.2016.06.013. Epub 2016 Jun 27.

No abstract available.

[Mortality in cystic fibrosis].

Ugeskrift for laeger

Koch C.
PMID: 9340880
Ugeskr Laeger. 1997 Sep 22;159(39):5779.

No abstract available.

Problems in diagnosis of cystic fibrosis.

The New Zealand medical journal

Wesley AW, Horne AM, Elliott RB.
PMID: 6593626
N Z Med J. 1984 Nov 14;97(767):773-5.

No abstract available.

The hepatic cirrhosis of cystic fibrosis of the pancreas.

The American journal of medicine

ROBERTS WC.
PMID: 14492801
Am J Med. 1962 Feb;32:324-8. doi: 10.1016/0002-9343(62)90300-5.

No abstract available.

Counterpoint: does the risk of cross infection warrant exclusion of adults with cystic fibrosis from cystic fibrosis foundation events? No.

Chest

Shepherd SL, Goodrich EJ, Desch J, Quinton PM.
PMID: 24135999
Chest. 2014 Apr;145(4):680-683. doi: 10.1378/chest.13-2406.

No abstract available.

Rebuttal from Dr Jain et al.

Chest

Jain M, Saiman LM, Sabadosa K, LiPuma JJ.
PMID: 24136038
Chest. 2014 Apr;145(4):683-684. doi: 10.1378/chest.13-2405.

No abstract available.

A review of renal disease in cystic fibrosis.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Nazareth D, Walshaw M.
PMID: 23618617
J Cyst Fibros. 2013 Jul;12(4):309-17. doi: 10.1016/j.jcf.2013.03.005. Epub 2013 Apr 22.

Kidney disease is becoming increasingly common in CF. This review looks at the effect of CFTR on the kidney, the problems with measuring renal function effectively in CF, the causes and incidence of renal dysfunction, and its pathophysiology. Strategies...

Interventions for preventing and managing advanced liver disease in cystic fibrosis.

The Cochrane database of systematic reviews

Palaniappan SK, Than NN, Thein AW, Moe S, van Mourik I.
PMID: 28850173
Cochrane Database Syst Rev. 2017 Aug 29;8:CD012056. doi: 10.1002/14651858.CD012056.pub2.

BACKGROUND: Cystic fibrosis is an autosomal recessive inherited defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene resulting in abnormal regulation of salt and water movement across the membranes. In the liver this leads to focal biliary fibrosis...

Cystic fibrosis related diabetes: Pathophysiology, screening and diagnosis.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Granados A, Chan CL, Ode KL, Moheet A, Moran A, Holl R.
PMID: 31679726
J Cyst Fibros. 2019 Oct;18:S3-S9. doi: 10.1016/j.jcf.2019.08.016.

Cystic fibrosis related diabetes (CFRD) is a distinct form of diabetes that is associated with significantly increased morbidity and mortality in the CF population. The primary etiology is relative insulin insufficiency secondary to destruction of pancreatic islets, and to...

Showing 1 to 12 of 44 entries