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Glucose >200 mg/dL during Continuous Glucose Monitoring Identifies Adult Patients at Risk for Development of Cystic Fibrosis Related Diabetes

Journal of diabetes research, 2016-01, Vol.2016 (2016), p.1-8

2016

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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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Airway Inflammation in Children with Cystic Fibrosis and Healthy Children Assessed by Sputum Induction

American journal of respiratory and critical care medicine, 2001-10, Vol.164 (8), p.1425-1431

2001

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SerpinB1 in cystic fibrosis airway fluids: quantity, molecular form and mechanism of elastase inhibition

The European respiratory journal, 2011-05, Vol.37 (5), p.1083-1090

2011

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Enteral nutrition for patients with cystic fibrosis: Comparison of a semi-elemental and nonelemental formula

The Journal of pediatrics, 1998-02, Vol.132 (2), p.265-269

1998

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Comparison of high-frequency chest wall oscillation and oscillating positive expiratory pressure in the home management of cystic fibrosis: A pilot study

Pediatric pulmonology, 2001-11, Vol.32 (5), p.372-377

2001

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C27 NEWS FROM THE NICU AND PICU: Characteristics Of The Lower Airway Microbiome In Mechanically Ventilated Children Differ By Reason For Admission And Day Of Intubation

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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B106 CELLULAR/MOLECULAR MECHANISMS AND TRANSLATIONAL ASPECTS OF RESPIRATORY TRACT INFECTIONS: Next Generation Sequencing Of Respiratory Fluids Accurately Distinguishes Bacterial From Viral Lower Respiratory Tract Infection By Both Microbial And Host Transcriptional Profiling

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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Relationship between antimicrobial proteins and airway inflammation and infection in cystic fibrosis

Pediatric pulmonology, 2009-04, Vol.44 (4), p.402-409

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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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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Induced sputum inflammatory measures correlate with lung function in children with cystic fibrosis

The Journal of pediatrics, 2002-12, Vol.141 (6), p.811-817

2002

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Two-tiered immunoreactive trypsinogen-based newborn screening for cystic fibrosis in Colorado: screening efficacy and diagnostic outcomes

The Journal of pediatrics, 2005-09, Vol.147 (3), p.S83-S88

2005

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Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening

Pediatric pulmonology, 2003-04, Vol.35 (4), p.257-262

2003

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Seeking modifier genes in cystic fibrosis

American journal of respiratory and critical care medicine, 2003-02, Vol.167 (3), p.289-290

2003

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NO pathway in CF and non-CF children

Pediatric pulmonology, 2004-04, Vol.37 (4), p.338-350

2004

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Update on newborn screening for cystic fibrosis

Current opinion in pulmonary medicine, 2004-11, Vol.10 (6), p.500-504

2004

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Newborn screening for cystic fibrosis

Current opinion in pediatrics, 2003-06, Vol.15 (3), p.309-315

2003

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Entera1 nutrition for patients with cystic fibrosis : Comparison of a semi-elemental and nonelemental formula

The Journal of pediatrics, 1998, Vol.132 (2), p.265-269

1998

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Gut Microbiota in the First 2 Years of Life and the Association with Body Mass Index at Age 12 in a Norwegian Birth Cohort

mBio, 2018-10, Vol.9 (5)

2018

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Early pulmonary vascular disease in preterm infants at risk for bronchopulmonary dysplasia

American journal of respiratory and critical care medicine, 2015-01, Vol.191 (1), p.87-95

2015

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Antenatal Determinants of Bronchopulmonary Dysplasia and Late Respiratory Disease in Preterm Infants

American journal of respiratory and critical care medicine, 2017-08, Vol.196 (3), p.364-374

2017

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Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

Nature communications, 2015-09, Vol.6 (1), p.8382-8382, Article 8382

2015

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Airway Microbial Community Turnover Differs by BPD Severity in Ventilated Preterm Infants

PloS one, 2017-01, Vol.12 (1), p.e0170120

2017

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Observation of plasma toroidal-momentum dissipation by neoclassical toroidal viscosity

Physical review letters, 2006-06, Vol.96 (22), p.225002-225002, Article 225002

2006

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Glucose >200 mg/dL during Continuous Glucose Monitoring Identifies Adult Patients at Risk for Development of Cystic Fibrosis Related Diabetes

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

Airway Inflammation in Children with Cystic Fibrosis and Healthy Children Assessed by Sputum Induction

SerpinB1 in cystic fibrosis airway fluids: quantity, molecular form and mechanism of elastase inhibition

Enteral nutrition for patients with cystic fibrosis: Comparison of a semi-elemental and nonelemental formula

Comparison of high-frequency chest wall oscillation and oscillating positive expiratory pressure in the home management of cystic fibrosis: A pilot study

C27 NEWS FROM THE NICU AND PICU: Characteristics Of The Lower Airway Microbiome In Mechanically Ventilated Children Differ By Reason For Admission And Day Of Intubation

B106 CELLULAR/MOLECULAR MECHANISMS AND TRANSLATIONAL ASPECTS OF RESPIRATORY TRACT INFECTIONS: Next Generation Sequencing Of Respiratory Fluids Accurately Distinguishes Bacterial From Viral Lower Respiratory Tract Infection By Both Microbial And Host Transcriptional Profiling

Relationship between antimicrobial proteins and airway inflammation and infection in cystic fibrosis

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

Complications associated with symptomatic diagnosis in infants with cystic fibrosis

Induced sputum inflammatory measures correlate with lung function in children with cystic fibrosis

Two-tiered immunoreactive trypsinogen-based newborn screening for cystic fibrosis in Colorado: screening efficacy and diagnostic outcomes

Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening

Seeking modifier genes in cystic fibrosis

NO pathway in CF and non-CF children

Update on newborn screening for cystic fibrosis

Newborn screening for cystic fibrosis

Entera1 nutrition for patients with cystic fibrosis : Comparison of a semi-elemental and nonelemental formula

Gut Microbiota in the First 2 Years of Life and the Association with Body Mass Index at Age 12 in a Norwegian Birth Cohort

Early pulmonary vascular disease in preterm infants at risk for bronchopulmonary dysplasia

Antenatal Determinants of Bronchopulmonary Dysplasia and Late Respiratory Disease in Preterm Infants

Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis

Airway Microbial Community Turnover Differs by BPD Severity in Ventilated Preterm Infants

Observation of plasma toroidal-momentum dissipation by neoclassical toroidal viscosity

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