Rationale: Expanding the use of cystic fibrosis transmembrane conductance regulator (CFTR) potentiators and correctors for the treatment of cystic fibrosis (CF) requires precise and accurate biomarkers. Sweat chloride concentration provides an in vivo assessment of CFTR function, but it is unknown the degree to which CFTR mutations account for sweat chloride variation
AbstractBackgroundSweat chloride test is the gold standard test for cystic fibrosis (CF) diagnosis. ...
To conduct a descriptive analysis of the sweat test (ST), associating ST results with epidemiologica...
BACKGROUND: The sweat test is one of the main diagnostic tools used in newborn screening programs an...
Rationale: Expanding the use of cystic fibrosis transmembrane conductance regulator (CFTR) potentiat...
Introduction: Sweat chloride concentration, a biomarker of CFTR function, is an appropriate outcome ...
AbstractBackgroundWe examined data from a Phase 2 trial {NCT00457821} of ivacaftor, a CFTR potentiat...
AbstractBackgroundIvacaftor, a cystic fibrosis transmembrane regulator (CFTR) potentiator, decreased...
Objective: To compare differences in epithelial chloride conductance according to class of mutation ...
Objectives: Recent sweat chloride guidelines published by the Cystic Fibrosis Foundation changed the...
BACKGROUND: The sweat test is the current gold standard for the diagnosis of cystic fibrosis (CF). C...
Cystic Fibrosis (CF) is a hereditary, systemic disease caused by mutations in the Cystic Fibrosis Tr...
AbstractIvacaftor, a CFTR potentiator that enhances chloride transport by acting directly on CFTR to...
Cystic Fibrosis (CF) is a genetic disease which affects the production of healthy cystic fibrosis tr...
Background: Cystic fibrosis (CF) is a hereditary disorder caused by genetic mutations, which affect ...
In a recent issue of CHEST (January 2013), Durmowicz et al 1 highlight the fi nding that despite imp...
AbstractBackgroundSweat chloride test is the gold standard test for cystic fibrosis (CF) diagnosis. ...
To conduct a descriptive analysis of the sweat test (ST), associating ST results with epidemiologica...
BACKGROUND: The sweat test is one of the main diagnostic tools used in newborn screening programs an...
Rationale: Expanding the use of cystic fibrosis transmembrane conductance regulator (CFTR) potentiat...
Introduction: Sweat chloride concentration, a biomarker of CFTR function, is an appropriate outcome ...
AbstractBackgroundWe examined data from a Phase 2 trial {NCT00457821} of ivacaftor, a CFTR potentiat...
AbstractBackgroundIvacaftor, a cystic fibrosis transmembrane regulator (CFTR) potentiator, decreased...
Objective: To compare differences in epithelial chloride conductance according to class of mutation ...
Objectives: Recent sweat chloride guidelines published by the Cystic Fibrosis Foundation changed the...
BACKGROUND: The sweat test is the current gold standard for the diagnosis of cystic fibrosis (CF). C...
Cystic Fibrosis (CF) is a hereditary, systemic disease caused by mutations in the Cystic Fibrosis Tr...
AbstractIvacaftor, a CFTR potentiator that enhances chloride transport by acting directly on CFTR to...
Cystic Fibrosis (CF) is a genetic disease which affects the production of healthy cystic fibrosis tr...
Background: Cystic fibrosis (CF) is a hereditary disorder caused by genetic mutations, which affect ...
In a recent issue of CHEST (January 2013), Durmowicz et al 1 highlight the fi nding that despite imp...
AbstractBackgroundSweat chloride test is the gold standard test for cystic fibrosis (CF) diagnosis. ...
To conduct a descriptive analysis of the sweat test (ST), associating ST results with epidemiologica...
BACKGROUND: The sweat test is one of the main diagnostic tools used in newborn screening programs an...