Different management approaches and outcome for infants with an inconclusive diagnosis following newborn screening for cystic fibrosis (CRMS/CFSPID) and Pseudomonas aeruginosa isolation

Outcomes of repeat sweat testing in cystic fibrosis newborn screen positive infants

(2021) Sarah E. Bauer et al.   PEDIATRIC PULMONOLOGY

A survey of the prevalence, management and outcome of infants with an inconclusive diagnosis following newborn bloodspot screening for cystic fibrosis (CRMS/CFSPID) in six Italian centres

(2021) Vito Terlizzi et al.   Journal of Cystic Fibrosis

Cystic fibrosis

(2021) Michal Shteinberg et al.   LANCET

Outcomes of early repeat sweat testing in infants with cystic fibrosis transmembrane conductance regulator‐related metabolic syndrome (CRMS)/CF screen‐positive, inconclusive diagnosis (CFSPID)

(2021) Vito Terlizzi et al.   PEDIATRIC PULMONOLOGY

Phenotype of children with inconclusive cystic fibrosis diagnosis after newborn screening

(2020) Anne Munck et al.   PEDIATRIC PULMONOLOGY

Trend of sweat chloride values in a cohort of patients carrying CFTR mutations of varying clinical consequence: Is there a risk of increasing sweat chloride over time?

(2020) Vito Terlizzi et al.   PEDIATRIC PULMONOLOGY

CRMS/CFSPID Subjects Carrying D1152H CFTR Variant: Can the Second Variant Be a Predictor of Disease Development?

(2020) Vito Terlizzi et al.   Diagnostics

ECFS best practice guidelines: the 2018 revision

(2018) Carlo Castellani et al.   Journal of Cystic Fibrosis

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis

(2017) Clement L. Ren et al.   JOURNAL OF PEDIATRICS

Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening

(2015) A. Munck et al.   Journal of Cystic Fibrosis

Inconclusive Diagnosis of Cystic Fibrosis After Newborn Screening

(2015) C. Y. Ooi et al.   PEDIATRICS

Outcomes of Infants With Indeterminate Diagnosis Detected by Cystic Fibrosis Newborn Screening

(2015) C. L. Ren et al.   PEDIATRICS

Multi-ethnic reference values for spirometry for the 3–95-yr age range: the global lung function 2012 equations

(2012) Philip H. Quanjer et al.   EUROPEAN RESPIRATORY JOURNAL

Prevalence of cystic fibrosis pathogens in the oropharynx of healthy children and implications for cystic fibrosis care

(2012) Margaret Rosenfeld et al.   Journal of Cystic Fibrosis

Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective

(2012) Anders Folkesson et al.   NATURE REVIEWS MICROBIOLOGY

Early antibiotic treatment forPseudomonas aeruginosaeradication in patients with cystic fibrosis: a randomised multicentre study comparing two different protocols

(2012) Giovanni Taccetti et al.   THORAX

Ciprofloxacin safety in paediatrics: a systematic review

(2011) A. Adefurin et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Comparative Efficacy and Safety of 4 Randomized Regimens to Treat Early Pseudomonas aeruginosa Infection in Children With Cystic Fibrosis

(2011) Miriam M. Treggiari   ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE

Recommendations for the classification of diseases as CFTR-related disorders

(2011) C. Bombieri et al.   Journal of Cystic Fibrosis

The Use of Systemic and Topical Fluoroquinolones

(2011) J. S. Bradley et al.   PEDIATRICS

Evolutionary dynamics of bacteria in a human host environment

(2011) L. Yang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

European best practice guidelines for cystic fibrosis neonatal screening

(2009) Carlo Castellani et al.   Journal of Cystic Fibrosis

Oropharyngeal flora in healthy infants: Observations and implications for cystic fibrosis care

(2009) David Carlson et al.   PEDIATRIC PULMONOLOGY