Similar articles for PMID: 23670503

Year	Number of Results
1995	1
1997	2
1998	6
2000	4
2001	3
2002	4
2003	3
2004	1
2005	5
2006	6
2007	3
2008	3
2009	8
2010	6
2011	2
2012	4
2013	6
2014	3
2015	3
2016	6
2017	11
2018	9
2019	7
2020	5
2021	7
2022	3
2024	0

1

Diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator gene in patients suspected of having mild or atypical cystic fibrosis.

Dal'Maso VB, Mallmann L, Siebert M, Simon L, Saraiva-Pereira ML, Dalcin Pde T. Dal'Maso VB, et al. J Bras Pneumol. 2013 Mar-Apr;39(2):181-9. doi: 10.1590/s1806-37132013000200009. J Bras Pneumol. 2013. PMID: 23670503 Free PMC article.

2

Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis.

Ratkiewicz M, Pastore M, McCoy KS, Thompson R, Hayes D Jr, Sheikh SI. Ratkiewicz M, et al. World J Pediatr. 2017 Apr;13(2):129-135. doi: 10.1007/s12519-017-0015-8. Epub 2017 Feb 15. World J Pediatr. 2017. PMID: 28194692

3

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. Bonadia LC, et al. Gene. 2014 May 1;540(2):183-90. doi: 10.1016/j.gene.2014.02.040. Epub 2014 Feb 26. Gene. 2014. PMID: 24583165

4

Non-classic cystic fibrosis associated with D1152H CFTR mutation.

Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D. Burgel PR, et al. Clin Genet. 2010 Apr;77(4):355-64. doi: 10.1111/j.1399-0004.2009.01294.x. Epub 2009 Oct 15. Clin Genet. 2010. PMID: 19843100

5

Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.

Bienvenu T, Sermet-Gaudelus I, Burgel PR, Hubert D, Crestani B, Bassinet L, Dusser D, Fajac I. Bienvenu T, et al. Am J Respir Crit Care Med. 2010 May 15;181(10):1078-84. doi: 10.1164/rccm.200909-1434OC. Epub 2010 Feb 18. Am J Respir Crit Care Med. 2010. PMID: 20167849

6

Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations.

Padoan R, Bassotti A, Seia M, Corbetta C. Padoan R, et al. Eur J Pediatr. 2002 Apr;161(4):212-5. doi: 10.1007/s00431-001-0910-8. Eur J Pediatr. 2002. PMID: 12014388

7

A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations.

Kerem E, Rave-Harel N, Augarten A, Madgar I, Nissim-Rafinia M, Yahav Y, Goshen R, Bentur L, Rivlin J, Aviram M, Genem A, Chiba-Falek O, Kraemer MR, Simon A, Branski D, Kerem B. Kerem E, et al. Am J Respir Crit Care Med. 1997 Jun;155(6):1914-20. doi: 10.1164/ajrccm.155.6.9196095. Am J Respir Crit Care Med. 1997. PMID: 9196095

8

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.

Wilschanski M, Zielenski J, Markiewicz D, Tsui LC, Corey M, Levison H, Durie PR. Wilschanski M, et al. J Pediatr. 1995 Nov;127(5):705-10. doi: 10.1016/s0022-3476(95)70157-5. J Pediatr. 1995. PMID: 7472820

9

Refining the continuum of CFTR-associated disorders in the era of newborn screening.

Levy H, Nugent M, Schneck K, Stachiw-Hietpas D, Laxova A, Lakser O, Rock M, Dahmer MK, Biller J, Nasr SZ, Baker M, McColley SA, Simpson P, Farrell PM. Levy H, et al. Clin Genet. 2016 May;89(5):539-49. doi: 10.1111/cge.12711. Epub 2016 Jan 20. Clin Genet. 2016. PMID: 26671754 Free PMC article.

10

Correctors (specific therapies for class II CFTR mutations) for cystic fibrosis.

Southern KW, Patel S, Sinha IP, Nevitt SJ. Southern KW, et al. Cochrane Database Syst Rev. 2018 Aug 2;8(8):CD010966. doi: 10.1002/14651858.CD010966.pub2. Cochrane Database Syst Rev. 2018. PMID: 30070364 Free PMC article. Updated. Review.

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