Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report (Q24657948)

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Terry B White

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Frank J Accurso

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Carlo Castellani

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Garry R Cutting

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Peter R Durie

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Vicky A Legrys

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John Massie

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Richard B Parad

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Michael J Rock

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Preston W Campbell

The Journal of Pediatrics

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language of work or name

English

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publication date

August 2008

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published in

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volume

153

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issue

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page(s)

S4-S14

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cites work

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Normal sweat chloride values do not exclude the diagnosis of cystic fibrosis

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Early pulmonary manifestation of cystic fibrosis in children with the DeltaF508/R117H-7T genotype

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Updated assessment of cystic fibrosis mutation frequencies in non-Hispanic Caucasians

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Pathophysiology of the pancreas in cystic fibrosis

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The meaning of "early" diagnosis in a new era of cystic fibrosis care

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A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

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Genetic and physiologic correlates of longitudinal immunoreactive trypsinogen decline in infants with cystic fibrosis identified through newborn screening

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Prediction of Mortality in Patients with Cystic Fibrosis

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Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis

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12 December 2020

Assessing quality assurance for sweat chloride testing

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12 December 2020

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10.1016/J.JPEDS.2008.05.005

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

18639722

1 reference