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Risk Factors For Rate of Decline in Forced Expiratory Volume in One Second in Children and Adolescents with Cystic Fibrosis

The Journal of pediatrics, 2007-08, Vol.151 (2), p.134-139.e1

2007

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Impact of Pseudomonas and Staphylococcus Infection on Inflammation and Clinical Status in Young Children with Cystic Fibrosis

The Journal of pediatrics, 2009-02, Vol.154 (2), p.183-188.e3

2009

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Impact of Socioeconomic Status, Race, and Ethnicity on Quality of Life in Patients With Cystic Fibrosis in the United States

Chest, 2010-03, Vol.137 (3), p.642-650

2010

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Compacted DNA nanoparticles administered to the nasal mucosa of cystic fibrosis subjects are safe and demonstrate partial to complete cystic fibrosis transmembrane regulator reconstitution

Human gene therapy, 2004-12, Vol.15 (12), p.1255-1269

2004

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Association of Socioeconomic Status with the Use of Chronic Therapies and Healthcare Utilization in Children with Cystic Fibrosis

The Journal of pediatrics, 2009-11, Vol.155 (5), p.634-639.e4

2009

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Probability of Treatment Following Acute Decline in Lung Function in Children with Cystic Fibrosis is Related to Baseline Pulmonary Function

The Journal of pediatrics, 2013-10, Vol.163 (4), p.1152-1157.e2

2013

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Myeloperoxidase and Protein Oxidation in the Airways of Young Children with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2004-12, Vol.170 (12), p.1317-1323

2004

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The Influence of Relaxing and Self-Selected Stimulating Music on Vertical Jump Performance in Male Volleyball Players

International journal of exercise science, 2022, Vol.15 (6), p.15-24

2022

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Sustained Benefit from ivacaftor demonstrated by combining clinical trial and cystic fibrosis patient registry data

American journal of respiratory and critical care medicine, 2015-10, Vol.192 (7), p.836-842

2015

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Impact of Pregnancy on Women With Cystic Fibrosis

Chest, 2006-03, Vol.129 (3), p.706-711

2006

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Early pulmonary inflammation in infants with cystic fibrosis

American journal of respiratory and critical care medicine, 1995-04, Vol.151 (4), p.1075-1082

1995

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Relationship between Inhaled Corticosteroid Therapy and Rate of Lung Function Decline in Children with Cystic Fibrosis

The Journal of pediatrics, 2008-12, Vol.153 (6), p.746-751.e2

2008

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Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis

The Journal of pediatrics, 2003-06, Vol.142 (6), p.624-630

2003

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Socioeconomic Status and the Likelihood of Antibiotic Treatment for Signs and Symptoms of Pulmonary Exacerbation in Children with Cystic Fibrosis

The Journal of pediatrics, 2011-11, Vol.159 (5), p.819-824.e1

2011

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Shifting patterns of inhaled antibiotic use in cystic fibrosis

Pediatric pulmonology, 2008-09, Vol.43 (9), p.874-881

2008

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Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function

Pediatric pulmonology, 2007-06, Vol.42 (6), p.513-518

2007

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Complications associated with symptomatic diagnosis in infants with cystic fibrosis

The Journal of pediatrics, 2005-09, Vol.147 (3), p.S37-S41

2005

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The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosis

Pediatric pulmonology, 2008-11, Vol.43 (11), p.1117-1123

2008

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Dornase alfa (Pulmozyme)

Current opinion in pulmonary medicine, 2012-11, Vol.18 (6), p.609-614

2012

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Corrigendum to FEV1 Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function [The Journal of Pediatrics (2016) 116–121]

The Journal of pediatrics, 2023-04, Vol.255, p.265-265

2023

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Paediatric trauma: injury pattern and mortality in the UK

Archives of disease in childhood. Education and practice edition, 2009-04, Vol.94 (2), p.37-41

2009

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Late Diagnosis Defines a Unique Population of Long-term Survivors of Cystic Fibrosis

American journal of respiratory and critical care medicine, 2005-03, Vol.171 (6), p.621-626

2005

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Strengthening care teams to improve adherence in cystic fibrosis: a qualitative practice assessment and quality improvement initiative

Patient preference and adherence, 2017-01, Vol.11, p.761-767

2017

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Lung function changes before and after pulmonary exacerbation antimicrobial treatment in cystic fibrosis

Pediatric pulmonology, 2020-03, Vol.55 (3), p.828-834

2020

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Prospective, long-term study of fat-soluble vitamin status in children with cystic fibrosis identified by newborn screen

The Journal of pediatrics, 1999-11, Vol.135 (5), p.601-610

1999

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Risk Factors For Rate of Decline in Forced Expiratory Volume in One Second in Children and Adolescents with Cystic Fibrosis

Impact of Pseudomonas and Staphylococcus Infection on Inflammation and Clinical Status in Young Children with Cystic Fibrosis

Impact of Socioeconomic Status, Race, and Ethnicity on Quality of Life in Patients With Cystic Fibrosis in the United States

Compacted DNA nanoparticles administered to the nasal mucosa of cystic fibrosis subjects are safe and demonstrate partial to complete cystic fibrosis transmembrane regulator reconstitution

Association of Socioeconomic Status with the Use of Chronic Therapies and Healthcare Utilization in Children with Cystic Fibrosis

Probability of Treatment Following Acute Decline in Lung Function in Children with Cystic Fibrosis is Related to Baseline Pulmonary Function

Myeloperoxidase and Protein Oxidation in the Airways of Young Children with Cystic Fibrosis

The Influence of Relaxing and Self-Selected Stimulating Music on Vertical Jump Performance in Male Volleyball Players

Sustained Benefit from ivacaftor demonstrated by combining clinical trial and cystic fibrosis patient registry data

Impact of Pregnancy on Women With Cystic Fibrosis

Early pulmonary inflammation in infants with cystic fibrosis

Relationship between Inhaled Corticosteroid Therapy and Rate of Lung Function Decline in Children with Cystic Fibrosis

Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis

Socioeconomic Status and the Likelihood of Antibiotic Treatment for Signs and Symptoms of Pulmonary Exacerbation in Children with Cystic Fibrosis

Shifting patterns of inhaled antibiotic use in cystic fibrosis

Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function

Complications associated with symptomatic diagnosis in infants with cystic fibrosis

The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosis

Dornase alfa (Pulmozyme)

Corrigendum to FEV1 Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function [The Journal of Pediatrics (2016) 116–121]

Paediatric trauma: injury pattern and mortality in the UK

Late Diagnosis Defines a Unique Population of Long-term Survivors of Cystic Fibrosis

Strengthening care teams to improve adherence in cystic fibrosis: a qualitative practice assessment and quality improvement initiative

Lung function changes before and after pulmonary exacerbation antimicrobial treatment in cystic fibrosis

Prospective, long-term study of fat-soluble vitamin status in children with cystic fibrosis identified by newborn screen

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