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3D‐printed, externally‐implanted, bioresorbable airway splints for severe tracheobronchomalacia

The Laryngoscope, 2019-08, Vol.129 (8), p.1763-1771

2019

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Quality improvement initiative to improve pulmonary function in pediatric cystic fibrosis patients

Pediatric pulmonology, 2020-11, Vol.55 (11), p.3039-3045

2020

Volltextzugriff (PDF)

Isolation of tracheal aspirate mesenchymal stromal cells predicts bronchopulmonary dysplasia

Pediatrics (Evanston), 2010-11, Vol.126 (5), p.e1127

2010

Volltextzugriff (PDF)

Assessing the Utility of an Outpatient Exercise Program for Children With Cystic Fibrosis: A Quality Improvement Project

Frontiers in pediatrics, 2022-01, Vol.9, p.734292-734292

2022

Volltextzugriff (PDF)

Longitudinal measures of lung function in infants with bronchopulmonary dysplasia

Pediatric pulmonology, 2011-04, Vol.46 (4), p.369-375

2011

Volltextzugriff (PDF)

Infant lung function tests as endpoints in the ISIS multicenter clinical trial in cystic fibrosis

Journal of cystic fibrosis, 2016-05, Vol.15 (3), p.386-391

2016

Volltextzugriff (PDF)

Development of an Interdisciplinary Telehealth Care Model in a Pediatric Cystic Fibrosis Center

Telemedicine reports, 2021-10, Vol.2 (1), p.224-232

2021

Volltextzugriff (PDF)

Bronchodilator responsiveness in wheezy infants and toddlers is not associated with asthma risk factors

Pediatric pulmonology, 2012-05, Vol.47 (5), p.421-428

2012

Volltextzugriff (PDF)

Handbook of Cystic Fibrosis

1st ed. 2017., 2016

Volltextzugriff (PDF)

Pulmonary function in bronchopulmonary dysplasia

Pediatric pulmonology, 2004-03, Vol.37 (3), p.236-242

2004

Volltextzugriff (PDF)

Predictors of insufficient sweat production during confirmatory testing for cystic fibrosis

Pediatric pulmonology, 2011-01, Vol.46 (1), p.23-30

2011

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Hypervitaminosis A causing hypercalcemia in cystic fibrosis. Case report and focused review

Annals of the American Thoracic Society, 2014-10, Vol.11 (8), p.1244-1247

2014

Volltextzugriff (PDF)

Predictors of early lung function in patients with congenital diaphragmatic hernia

Journal of pediatric surgery, 2014-06, Vol.49 (6), p.882-885

2014

Volltextzugriff (PDF)

Factors Affecting Weaning From Chronic Home Mechanical Ventilation in Children Under the Age of Four Years

Chest, 2013, Vol.144 (4), p.769A-769A

2013

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Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial

JAMA : the journal of the American Medical Association, 2012-06, Vol.307 (21), p.2269

2012

Volltextzugriff (PDF)

Emergency airway and ventilator procedures for community based home care staff validation of an educational program

Pediatric pulmonology, 2018-03, Vol.53 (3), p.374-380

2018

Volltextzugriff (PDF)

Microbiological efficacy of early MRSA treatment in cystic fibrosis in a randomised controlled trial

Thorax, 2017-04, Vol.72 (4), p.318

2017

Volltextzugriff (PDF)

Improvements in body mass index of children with cystic fibrosis following implementation of a standardized nutritional algorithm: A quality improvement project

Pediatric pulmonology, 2023-05, Vol.58 (5), p.1463-1470

2023

Volltextzugriff (PDF)

Implementation of standardized cystic fibrosis care algorithm to improve the center data-quality improvement project international collaboration

Journal of cystic fibrosis, 2023-07, Vol.22 (4), p.710-714

2023

Volltextzugriff (PDF)

Improving nutritional status in a pediatric cystic fibrosis center

Pediatric pulmonology, 2015-06, Vol.50 (6), p.544-551

2015

Volltextzugriff (PDF)

Introduction and Epidemiology of Cystic Fibrosis

Handbook of Cystic Fibrosis, 2016, p.1-4

2016

Volltextzugriff (PDF)

Treatment of Cystic Fibrosis

Handbook of Cystic Fibrosis, 2016, p.77-99

2016

Volltextzugriff (PDF)

Pathophysiology of Cystic Fibrosis

Handbook of Cystic Fibrosis, 2016, p.5-8

2016

Volltextzugriff (PDF)

Clinical Features and Complications of Cystic Fibrosis

Handbook of Cystic Fibrosis, 2016, p.9-41

2016

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Monitoring and Evaluation of Patients with Cystic Fibrosis

Handbook of Cystic Fibrosis, 2016, p.65-76

2016

Volltextzugriff (PDF)

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Infant, Newborn
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Cystic Fibrosis Transmembrane Conductance Regulator
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3D‐printed, externally‐implanted, bioresorbable airway splints for severe tracheobronchomalacia

Quality improvement initiative to improve pulmonary function in pediatric cystic fibrosis patients

Isolation of tracheal aspirate mesenchymal stromal cells predicts bronchopulmonary dysplasia

Assessing the Utility of an Outpatient Exercise Program for Children With Cystic Fibrosis: A Quality Improvement Project

Longitudinal measures of lung function in infants with bronchopulmonary dysplasia

Infant lung function tests as endpoints in the ISIS multicenter clinical trial in cystic fibrosis

Development of an Interdisciplinary Telehealth Care Model in a Pediatric Cystic Fibrosis Center

Bronchodilator responsiveness in wheezy infants and toddlers is not associated with asthma risk factors

Handbook of Cystic Fibrosis

Pulmonary function in bronchopulmonary dysplasia

Predictors of insufficient sweat production during confirmatory testing for cystic fibrosis

Hypervitaminosis A causing hypercalcemia in cystic fibrosis. Case report and focused review

Predictors of early lung function in patients with congenital diaphragmatic hernia

Factors Affecting Weaning From Chronic Home Mechanical Ventilation in Children Under the Age of Four Years

Inhaled hypertonic saline in infants and children younger than 6 years with cystic fibrosis: the ISIS randomized controlled trial

Emergency airway and ventilator procedures for community based home care staff validation of an educational program

Microbiological efficacy of early MRSA treatment in cystic fibrosis in a randomised controlled trial

Improvements in body mass index of children with cystic fibrosis following implementation of a standardized nutritional algorithm: A quality improvement project

Implementation of standardized cystic fibrosis care algorithm to improve the center data-quality improvement project international collaboration

Improving nutritional status in a pediatric cystic fibrosis center

Introduction and Epidemiology of Cystic Fibrosis

Treatment of Cystic Fibrosis

Pathophysiology of Cystic Fibrosis

Clinical Features and Complications of Cystic Fibrosis

Monitoring and Evaluation of Patients with Cystic Fibrosis

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