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Items: 1 to 20 of 957

1.
2.

Vaccination of cystic fibrosis patients against Pseudomonas aeruginosa reduces the proportion of patients infected and delays time to infection.

Lang AB, Rüdeberg A, Schöni MH, Que JU, Fürer E, Schaad UB.

Pediatr Infect Dis J. 2004 Jun;23(6):504-10.

PMID:
15194830
3.

European Epidemiologic Registry of Cystic Fibrosis (ERCF): comparison of major disease manifestations between patients with different classes of mutations.

Koch C, Cuppens H, Rainisio M, Madessani U, Harms H, Hodson M, Mastella G, Navarro J, Strandvik B, McKenzie S; Investigators of the ERCF.

Pediatr Pulmonol. 2001 Jan;31(1):1-12.

PMID:
11180668
4.

Predictors of deterioration of lung function in cystic fibrosis.

Schaedel C, de Monestrol I, Hjelte L, Johannesson M, Kornfält R, Lindblad A, Strandvik B, Wahlgren L, Holmberg L.

Pediatr Pulmonol. 2002 Jun;33(6):483-91.

PMID:
12001283
5.

Increased morbidity associated with chronic infection by an epidemic Pseudomonas aeruginosa strain in CF patients.

Al-Aloul M, Crawley J, Winstanley C, Hart CA, Ledson MJ, Walshaw MJ.

Thorax. 2004 Apr;59(4):334-6.

6.

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M.

Gastroenterology. 2004 Oct;127(4):1085-95.

PMID:
15480987
7.

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.

Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.

J Cyst Fibros. 2008 Mar;7(2):102-9. Epub 2007 Jul 27.

9.

Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosis.

Choi EH, Ehrmantraut M, Foster CB, Moss J, Chanock SJ.

Pediatr Pulmonol. 2006 Mar;41(3):255-62.

PMID:
16429424
10.

ENaCbeta and gamma genes as modifier genes in cystic fibrosis.

Viel M, Leroy C, Hubert D, Fajac I, Bienvenu T.

J Cyst Fibros. 2008 Jan;7(1):23-9. Epub 2007 Jun 7.

11.

Clinical characteristics and genotype analysis of patients with cystic fibrosis and nasal polyposis requiring surgery.

Kingdom TT, Lee KC, FitzSimmons SC, Cropp GJ.

Arch Otolaryngol Head Neck Surg. 1996 Nov;122(11):1209-13.

PMID:
8906056
12.

Long-term effects of birth order and age at diagnosis in cystic fibrosis: a sibling cohort study.

Slieker MG, van den Berg JM, Kouwenberg J, van Berkhout FT, Heijerman HG, van der Ent CK.

Pediatr Pulmonol. 2010 Jun;45(6):601-7. doi: 10.1002/ppul.21227.

PMID:
20503286
13.

Genotype-phenotype correlation for pulmonary function in cystic fibrosis.

de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.

Thorax. 2005 Jul;60(7):558-63.

14.

Effect of allergic bronchopulmonary aspergillosis on lung function in children with cystic fibrosis.

Kraemer R, Deloséa N, Ballinari P, Gallati S, Crameri R.

Am J Respir Crit Care Med. 2006 Dec 1;174(11):1211-20. Epub 2006 Sep 7.

PMID:
16959918
15.

Cystic fibrosis genotype and bacterial infection: a possible connection.

McManus TE, Beattie D, Graham C, Moore JE, Elborn JS.

Br J Biomed Sci. 2005;62(2):85-8.

PMID:
15997883
16.

Pulmonary infection in mild variant cystic fibrosis: implications for care.

Lording A, McGaw J, Dalton A, Beal G, Everard M, Taylor CJ.

J Cyst Fibros. 2006 May;5(2):101-4. Epub 2006 Jan 19.

17.

Late diagnosis defines a unique population of long-term survivors of cystic fibrosis.

Rodman DM, Polis JM, Heltshe SL, Sontag MK, Chacon C, Rodman RV, Brayshaw SJ, Huitt GA, Iseman MD, Saavedra MT, Taussig LM, Wagener JS, Accurso FJ, Nick JA.

Am J Respir Crit Care Med. 2005 Mar 15;171(6):621-6. Epub 2004 Dec 10.

PMID:
15591474
18.

Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis.

Raman V, Clary R, Siegrist KL, Zehnbauer B, Chatila TA.

Pediatrics. 2002 Jan;109(1):E13.

PMID:
11773581
19.

CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.

Bonadia LC, de Lima Marson FA, Ribeiro JD, Paschoal IA, Pereira MC, Ribeiro AF, Bertuzzo CS.

Gene. 2014 May 1;540(2):183-90. doi: 10.1016/j.gene.2014.02.040. Epub 2014 Feb 26.

PMID:
24583165
20.

[Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].

Iwańczak F, Smigiel R, Stawarski A, Pawłowicz J, Stembalska A, Mowszet K, Sasiadek M.

Pol Merkur Lekarski. 2005 Feb;18(104):205-9. Polish.

PMID:
17877132

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