New clinical diagnostic procedures for cystic fibrosis in Europe (Q37887186)

24 August 2017

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title

New clinical diagnostic procedures for cystic fibrosis in Europe (English)

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24 August 2017

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K De Boeck

1

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24 August 2017

N Derichs

2

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24 August 2017

I Fajac

3

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24 August 2017

H R de Jonge

4

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24 August 2017

I Bronsveld

5

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24 August 2017

I Sermet

6

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24 August 2017

F Vermeulen

7

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24 August 2017

D N Sheppard

8

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24 August 2017

H Cuppens

9

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24 August 2017

M Hug

10

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P Melotti

11

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P G Middleton

12

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M Wilschanski

13

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ECFS Diagnostic Network Working Group

14

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EuroCareCF WP3 Group on CF diagnosis

15

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24 August 2017

publication date

1 June 2011

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Journal of Cystic Fibrosis

24 August 2017

published in

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24 August 2017

volume

10 Suppl 2

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24 August 2017

page(s)

S53-66

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Cystic fibrosis: terminology and diagnostic algorithms

24 August 2017

cites work

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Nasal potential measurements on the nasal floor and under the inferior turbinate: does it matter?

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Impact of different chloride and glucose solutions on nasal potential difference.

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Reproducibility of nasal potential difference measurements in cystic fibrosis

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Airway ion transport impacts on disease presentation and severity in cystic fibrosis

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Measurement of airway ion transport assists the diagnosis of cystic fibrosis

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Airway surface liquid calcium modulates chloride permeability in the cystic fibrosis airway.

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Hypertonic saline alters ion transport across the human airway epithelium

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7 January 2021

A multicenter study of the effect of solution temperature on nasal potential difference measurements

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7 January 2021

A modified technique for measurement of nasal transepithelial potential difference in infants

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7 January 2021

Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens

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7 January 2021

Nasal potential difference in congenital bilateral absence of the vas deferens

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7 January 2021

Recommendations for the classification of diseases as CFTR-related disorders

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7 January 2021

Amiloride-insensitive nasal potential difference varies with the menstrual cycle in cystic fibrosis.

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7 January 2021

Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers.

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7 January 2021

The effect of varying tonicity on nasal epithelial ion transport in cystic fibrosis

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7 January 2021

Hypertonic saline inhibits luminal sodium channels in respiratory epithelium

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7 January 2021

Nasal epithelium potential difference at high altitude (4,559 m): evidence for secretion

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7 January 2021

Pulmonary disease severity in men with deltaF508 cystic fibrosis and residual chloride secretion

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7 January 2021

Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR.

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7 January 2021

Nasal airway ion transport and lung function in young people with cystic fibrosis

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7 January 2021

CFTR function and prospects for therapy

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7 January 2021

Electrolyte transport in the mammalian colon: mechanisms and implications for disease

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7 January 2021

Role of CFTR in the colon

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7 January 2021

Chloride secretion by the intestinal epithelium: molecular basis and regulatory aspects

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7 January 2021

Intestinal ion transport and the pathophysiology of diarrhea

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7 January 2021

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

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7 January 2021

Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice

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7 January 2021

Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers

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7 January 2021

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium

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7 January 2021

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

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7 January 2021

Failure of cholinergic stimulation to induce a secretory response from the rectal mucosa in cystic fibrosis

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7 January 2021

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon

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7 January 2021

Assessment of CFTR function in native epithelia for the diagnosis of cystic fibrosis.

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7 January 2021

Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis.

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7 January 2021

Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Mediated Residual Chloride Secretion Does Not Protect against Early Chronic Pseudomonas aeruginosa Infection in F508del Homozygous Cystic Fibrosis Patients

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7 January 2021

Molecular targeting of CFTR as a therapeutic approach to cystic fibrosis.

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7 January 2021

Transepithelial electrical measurements with the Ussing chamber

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7 January 2021

Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patients

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https://api.crossref.org/works/10.1016%2FS1569-1993%2811%2960009-X

7 January 2021

Adrenaline-induced colonic K+ secretion is mediated by KCa1.1 (BK) channels.

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7 January 2021

Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion.

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7 January 2021

Therapeutic potential of cystic fibrosis transmembrane conductance regulator (CFTR) inhibitors in polycystic kidney disease

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7 January 2021

Epac1 mediates protein kinase A-independent mechanism of forskolin-activated intestinal chloride secretion

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7 January 2021

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

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7 January 2021

Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this cystic fibrosis transmembrane conductance regulator mutation does not cause cystic fibrosis

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7 January 2021

A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis.

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7 January 2021

Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis

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7 January 2021

Could a defective epithelial sodium channel lead to bronchiectasis

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7 January 2021

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease

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7 January 2021

Plasmodium falciparum-activated chloride channels are defective in erythrocytes from cystic fibrosis patients.

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7 January 2021

Physiological concept for a blood based CFTR test.

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7 January 2021

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Identifiers

DOI

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24 August 2017

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