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Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

The Journal of pediatrics, 2017-02, Vol.181, p.S4-S15.e1

2017

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Refinement of newborn screening for cystic fibrosis with next generation sequencing

Pediatric pulmonology, 2023-03, Vol.58 (3), p.778-787

2023

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Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

The Journal of pediatrics, 2008-08, Vol.153 (2), p.S4-S14

2008

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New Challenges in the Diagnosis and Management of Cystic Fibrosis

The Journal of pediatrics, 2015-06, Vol.166 (6), p.1337-1341

2015

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Variation in cystic fibrosis newborn screening algorithms in the United States

Pediatric pulmonology, 2023-03, Vol.58 (3), p.927-933

2023

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Diagnosis of Cystic Fibrosis in Screened Populations

The Journal of pediatrics, 2017-02, Vol.181, p.S33-S44.e2

2017

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Introduction to “Cystic Fibrosis Foundation Consensus Guidelines for Diagnosis of Cystic Fibrosis”

The Journal of pediatrics, 2017-02, Vol.181, p.S1-S3

2017

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Applying Cystic Fibrosis Transmembrane Conductance Regulator Genetics and CFTR2 Data to Facilitate Diagnoses

The Journal of pediatrics, 2017-02, Vol.181, p.S27-S32.e1

2017

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Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis

The Journal of pediatrics, 2009-12, Vol.155 (6), p.S73-S93

2009

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Diagnosis of Cystic Fibrosis in Nonscreened Populations

The Journal of pediatrics, 2017-02, Vol.181, p.S52-S57.e2

2017

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The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive Therapy

Genes, 2020-04, Vol.11 (4), p.401

2020

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Why cystic fibrosis newborn screening programs have failed to meet original expectations… thus far

Molecular genetics and metabolism, 2023-09, Vol.140 (1-2), p.107679-107679, Article 107679

Farrell, Philip M

2023

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Cystic Fibrosis Diagnostic Challenges over 4 Decades: Historical Perspectives and Lessons Learned

The Journal of pediatrics, 2017-02, Vol.181, p.S16-S26

2017

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Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome during the First Two Years of Life and Beyond

The Journal of pediatrics, 2009-12, Vol.155 (6), p.S106-S116

2009

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Parental Preferences about Policy Options Regarding Disclosure of Incidental Genetic Findings in Newborn Screening: Using Videos and the Internet to Educate and Obtain Input

International journal of neonatal screening, 2022-09, Vol.8 (4), p.54

2022

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Setting a new standard in cystic fibrosis newborn screening illustrates controversial issues as new data emerge

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1305-1306

Farrell, Philip M

2020

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Changing incidence of cystic fibrosis in Wisconsin, USA

Pediatric pulmonology, 2015-11, Vol.50 (11), p.1065-1072

2015

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The prevalence of cystic fibrosis in the European Union

Journal of cystic fibrosis, 2008-09, Vol.7 (5), p.450-453

Farrell, Philip M

2008

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Newborn Screening for CF across the Globe- Where Is It Worthwhile ?

International journal of neonatal screening, 2020-03, Vol.6 (1), p.18-18

2020

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Challenging the dogma of the healthy heterozygote: Implications for newborn screening policies and practices

Molecular genetics and metabolism, 2021-09, Vol.134 (1-2), p.8-19

2021

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Update on advances in cystic fibrosis towards a cure and implications for primary care clinicians

Current problems in pediatric and adolescent health care, 2024-06, Vol.54 (6), p.101637-101637, Article 101637

2024

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Early Diagnosis of Cystic Fibrosis Through Neonatal Screening Prevents Severe Malnutrition and Improves Long-Term Growth

Pediatrics (Evanston), 2001-01, Vol.107 (1), p.1-13

2001

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Newborn Screening for Cystic Fibrosis: A Qualitative Study of Successes and Challenges from Universal Screening in the United States

International journal of neonatal screening, 2022-06, Vol.8 (3), p.38

2022

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Cystic fibrosis screen‐positive neonates with one pathogenic variant still warrant sweat testing

Pediatric pulmonology, 2023-11, Vol.58 (11), p.3342-3345

2023

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Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

Refinement of newborn screening for cystic fibrosis with next generation sequencing

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

New Challenges in the Diagnosis and Management of Cystic Fibrosis

Variation in cystic fibrosis newborn screening algorithms in the United States

Diagnosis of Cystic Fibrosis in Screened Populations

Introduction to “Cystic Fibrosis Foundation Consensus Guidelines for Diagnosis of Cystic Fibrosis”

Applying Cystic Fibrosis Transmembrane Conductance Regulator Genetics and CFTR2 Data to Facilitate Diagnoses

Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis

Diagnosis of Cystic Fibrosis in Nonscreened Populations

The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive Therapy

Why cystic fibrosis newborn screening programs have failed to meet original expectations… thus far

Cystic Fibrosis Diagnostic Challenges over 4 Decades: Historical Perspectives and Lessons Learned

Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome during the First Two Years of Life and Beyond

Parental Preferences about Policy Options Regarding Disclosure of Incidental Genetic Findings in Newborn Screening: Using Videos and the Internet to Educate and Obtain Input

Setting a new standard in cystic fibrosis newborn screening illustrates controversial issues as new data emerge

Changing incidence of cystic fibrosis in Wisconsin, USA

The prevalence of cystic fibrosis in the European Union

Newborn Screening for CF across the Globe- Where Is It Worthwhile ?

Challenging the dogma of the healthy heterozygote: Implications for newborn screening policies and practices

Update on advances in cystic fibrosis towards a cure and implications for primary care clinicians

Early Diagnosis of Cystic Fibrosis Through Neonatal Screening Prevents Severe Malnutrition and Improves Long-Term Growth

Newborn Screening for Cystic Fibrosis: A Qualitative Study of Successes and Challenges from Universal Screening in the United States

Cystic fibrosis screen‐positive neonates with one pathogenic variant still warrant sweat testing

The future of cystic fibrosis care: a global perspective

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