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Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis

JAMA : the journal of the American Medical Association, 2005-02, Vol.293 (5), p.581

2005

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Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: early detection by serology and assessment of risk factors

JAMA : the journal of the American Medical Association, 2002-06, Vol.287 (22), p.2958

2002

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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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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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Prenatal screening for cystic fibrosis: Where are we now?

The Journal of pediatrics, 2002-12, Vol.141 (6), p.758-763

2002

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Cystic fibrosis: A worldwide analysis of CFTR mutations-correlation with incidence data and application to screening

Human mutation, 2002-06, Vol.19 (6), p.575-606

2002

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ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals

Journal of cystic fibrosis, 2024-05, Vol.23 (3), p.388-397

2024

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Refining the continuum of CFTR-associated disorders in the era of newborn screening

Clinical genetics, 2016-05, Vol.89 (5), p.539-549

2016

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Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment

Pediatrics (Evanston), 2005-06, Vol.115 (6), p.1692-1703

2005

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Newborn screening for cystic fibrosis: ensuring more good than harm

The Journal of pediatrics, 2003-12, Vol.143 (6), p.707-712

2003

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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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Assessing Personal Qualities in Medical School Admissions

Academic medicine, 2003-03, Vol.78 (3), p.313-321

2003

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Evidence on Improved Outcomes with Early Diagnosis of Cystic Fibrosis Through Neonatal Screening: Enough is Enough

The Journal of pediatrics, 2005-09, Vol.147 (3), p.S30-S36

2005

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Association between mucoid Pseudomonas infection and bronchiectasis in children with cystic fibrosis

Radiology, 2009-08, Vol.252 (2), p.534-543

2009

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The Survival Advantage of Patients with Cystic Fibrosis Diagnosed Through Neonatal Screening: Evidence from the United States Cystic Fibrosis Foundation Registry Data

The Journal of pediatrics, 2005-09, Vol.147 (3), p.S57-S63

2005

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Cognitive function of children with cystic fibrosis: deleterious effect of early malnutrition

Pediatrics (Evanston), 2004-06, Vol.113 (6), p.1549-1558

2004

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Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition

Pediatric pulmonology, 2001-10, Vol.32 (4), p.277-287

2001

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Association between Initial Disease Presentation, Lung Disease Outcomes, and Survival in Patients with Cystic Fibrosis

American journal of epidemiology, 2004-03, Vol.159 (6), p.537-546

2004

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Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing

The Journal of pediatrics, 2005-09, Vol.147 (3), p.S73-S77

2005

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Bronchopulmonary Disease in Children with Cystic Fibrosis after Early or Delayed Diagnosis

American journal of respiratory and critical care medicine, 2003-11, Vol.168 (9), p.1100-1108

2003

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Nutritional Benefits of Neonatal Screening for Cystic Fibrosis

The New England journal of medicine, 1997-10, Vol.337 (14), p.963-969

1997

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Preventing early, prolonged vitamin E deficiency: an opportunity for better cognitive outcomes via early diagnosis through neonatal screening

The Journal of pediatrics, 2005-09, Vol.147 (3), p.S51-S56

2005

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Genetic counseling and neonatal screening for cystic fibrosis: an assessment of the communication process

Pediatrics (Evanston), 2001-04, Vol.107 (4), p.699-705

2001

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Pseudomonas aeruginosa serological analysis in young children with cystic fibrosis diagnosed through newborn screening

Pediatric pulmonology, 2010-01, Vol.45 (1), p.55-61

2010

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Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis

Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: early detection by serology and assessment of risk factors

The prevalence of cystic fibrosis in the European Union

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

Prenatal screening for cystic fibrosis: Where are we now?

Cystic fibrosis: A worldwide analysis of CFTR mutations-correlation with incidence data and application to screening

ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals

Refining the continuum of CFTR-associated disorders in the era of newborn screening

Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment

Newborn screening for cystic fibrosis: ensuring more good than harm

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

Assessing Personal Qualities in Medical School Admissions

Evidence on Improved Outcomes with Early Diagnosis of Cystic Fibrosis Through Neonatal Screening: Enough is Enough

Association between mucoid Pseudomonas infection and bronchiectasis in children with cystic fibrosis

The Survival Advantage of Patients with Cystic Fibrosis Diagnosed Through Neonatal Screening: Evidence from the United States Cystic Fibrosis Foundation Registry Data

Cognitive function of children with cystic fibrosis: deleterious effect of early malnutrition

Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition

Association between Initial Disease Presentation, Lung Disease Outcomes, and Survival in Patients with Cystic Fibrosis

Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing

Bronchopulmonary Disease in Children with Cystic Fibrosis after Early or Delayed Diagnosis

Nutritional Benefits of Neonatal Screening for Cystic Fibrosis

Preventing early, prolonged vitamin E deficiency: an opportunity for better cognitive outcomes via early diagnosis through neonatal screening

Genetic counseling and neonatal screening for cystic fibrosis: an assessment of the communication process

Gross genomic rearrangements involving deletions in the CFTR gene : characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms

Pseudomonas aeruginosa serological analysis in young children with cystic fibrosis diagnosed through newborn screening

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