Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data

Derichs, Nico; Sanz, Javier; Von Kanel, Thomas; Stolpe, Cornelia; Zapf, Antonia; Tümmler, Burkhard; Gallati, Sabina; Ballmann, Manfred (2010). Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data. Thorax, 65(7), pp. 594-9. London: BMJ Publishing Group 10.1136/thx.2009.125088

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In questionable cystic fibrosis (CF), mild or monosymptomatic phenotypes frequently cause diagnostic difficulties despite detailed algorithms. CF transmembrane conductance regulator (CFTR)-mediated ion transport can be studied ex vivo in rectal biopsies by intestinal current measurement (ICM).

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine

UniBE Contributor:

Gallati, Sabina

ISSN:

0040-6376

Publisher:

BMJ Publishing Group

Language:

English

Submitter:

Factscience Import

Date Deposited:

04 Oct 2013 14:13

Last Modified:

17 Mar 2015 19:15

Publisher DOI:

10.1136/thx.2009.125088

PubMed ID:

20627915

Web of Science ID:

000279806400009

URI:

https://boris.unibe.ch/id/eprint/2825 (FactScience: 205744)

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