Similar articles for PMID: 24022019

Year	Number of Results
1988	1
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1998	1
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2024	0

1

Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey.

Naehrlich L, Ballmann M, Davies J, Derichs N, Gonska T, Hjelte L, van Konigsbruggen-Rietschel S, Leal T, Melotti P, Middleton P, Tümmler B, Vermeulen F, Wilschanski M; ECFS Diagnostic Network Working Group. Naehrlich L, et al. J Cyst Fibros. 2014 Jan;13(1):24-8. doi: 10.1016/j.jcf.2013.08.006. Epub 2013 Sep 7. J Cyst Fibros. 2014. PMID: 24022019 Free article.

2

The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.

Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A. Sermet-Gaudelus I, et al. BMC Pediatr. 2006 Oct 3;6:25. doi: 10.1186/1471-2431-6-25. BMC Pediatr. 2006. PMID: 17018149 Free PMC article.

3

Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis.

Tridello G, Menin L, Pintani E, Bergamini G, Assael BM, Melotti P. Tridello G, et al. J Cyst Fibros. 2016 Sep;15(5):579-82. doi: 10.1016/j.jcf.2016.06.009. Epub 2016 Jul 15. J Cyst Fibros. 2016. PMID: 27423539 Free article.

4

Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?

Ooi CY, Dupuis A, Gonska T, Ellis L, Ni A, Jarvi K, Martin S, Ray P, Steele L, Kortan P, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P. Ooi CY, et al. Ann Am Thorac Soc. 2014 May;11(4):562-70. doi: 10.1513/AnnalsATS.201311-412OC. Ann Am Thorac Soc. 2014. PMID: 24697796

5

Transepithelial nasal potential difference (NPD) measurements in cystic fibrosis (CF).

Sands D. Sands D. Med Wieku Rozwoj. 2013 Jan-Mar;17(1):13-7. Med Wieku Rozwoj. 2013. PMID: 23749691 Review.

6

Protocols for in vivo measurement of the ion transport defects in cystic fibrosis nasal epithelium.

Middleton PG, Geddes DM, Alton EW. Middleton PG, et al. Eur Respir J. 1994 Nov;7(11):2050-6. Eur Respir J. 1994. PMID: 7875281 Free article.

7

Insights into the variability of nasal potential difference, a biomarker of CFTR activity.

Kyrilli S, Henry T, Wilschanski M, Fajac I, Davies JC, Jais JP, Sermet-Gaudelus I. Kyrilli S, et al. J Cyst Fibros. 2020 Jul;19(4):620-626. doi: 10.1016/j.jcf.2019.09.015. Epub 2019 Nov 4. J Cyst Fibros. 2020. PMID: 31699569 Free article.

8

Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?

Ooi CY, Dupuis A, Ellis L, Jarvi K, Martin S, Ray PN, Steele L, Kortan P, Gonska T, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P. Ooi CY, et al. Thorax. 2014 Mar;69(3):254-60. doi: 10.1136/thoraxjnl-2013-203832. Epub 2013 Oct 21. Thorax. 2014. PMID: 24149827

9

Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.

Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, Deneuville E, Reix P, Bui S, Huet F, Lebourgeois M, Munck A, Iron A, Skalicka V, Bienvenu T, Roussel D, Lenoir G, Bellon G, Sarles J, Macek M, Roussey M, Fajac I, Edelman A. Sermet-Gaudelus I, et al. Am J Respir Crit Care Med. 2010 Oct 1;182(7):929-36. doi: 10.1164/rccm.201003-0382OC. Epub 2010 Jun 10. Am J Respir Crit Care Med. 2010. PMID: 20538955

10

Measurement of airway ion transport assists the diagnosis of cystic fibrosis.

Middleton PG, House HH. Middleton PG, et al. Pediatr Pulmonol. 2010 Aug;45(8):789-95. doi: 10.1002/ppul.21253. Pediatr Pulmonol. 2010. PMID: 20597077

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