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Long term clinical effectiveness of ivacaftor in people with the G551D CFTR mutation

Journal of cystic fibrosis, 2021-03, Vol.20 (2), p.213-219

2021

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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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Dynamic incremental CT: effect of volume and concentration of contrast material and patient weight on hepatic enhancement

Radiology, 1995-05, Vol.195 (2), p.353

1995

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Blood mRNA biomarkers for detection of treatment response in acute pulmonary exacerbations of cystic fibrosis

Thorax, 2013-10, Vol.68 (10), p.929-937

2013

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Hepatic spiral CT: reduction of dose of intravenous contrast material

Radiology, 1995-10, Vol.197 (1), p.83

1995

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Dynamic contrast-enhanced CT of the liver: comparison of contrast medium injection rates and uniphasic and biphasic injection protocols

Radiology, 1993-05, Vol.187 (2), p.327

1993

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730 Longitudinal impact of pulmonary exacerbation frequency on lung function in children with cystic fibrosis

Journal of cystic fibrosis, 2023-10, Vol.22, p.S404-S404

2023

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139 Discovering symptom clustering patters during a pulmonary exacerbation in people with cystic fibrosis

Journal of cystic fibrosis, 2022-10, Vol.21, p.S82-S82

2022

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512 Hepatic and nutritional outcomes of Hispanic and non-Hispanic children with cystic fibrosis

Journal of cystic fibrosis, 2023-10, Vol.22, p.S270-S271

2023

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12 Using continuous glucose monitoring to predict disease progression and development of diabetes in youth with cystic fibrosis

Journal of cystic fibrosis, 2022-10, Vol.21, p.S8-S9

2022

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557 Relationship between metabolomic profiles and clinical outcomes after CFTR rescue

Journal of cystic fibrosis, 2023-10, Vol.22, p.S294-S295

2023

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C67 SUPPURATIVE LUNG DISEASES IN CHILDREN: Automated Airway Scores Of Bronchiectasis In Children With Cystic Fibrosis Using A Machine Learning Classifier

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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578: Serum biomarkers identified by proteomics and measured by commercially available assays associated with lung function during clinically stable states

Journal of cystic fibrosis, 2021-11, Vol.20, p.S274-S276

2021

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693 Improving timeliness and equity of cystic fibrosis newborn screening in Colorado and Wyoming

Journal of cystic fibrosis, 2023-10, Vol.22, p.S382-S383

2023

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Detection of CT-proved pulmonary nodules: comparison of selenium-based digital and conventional screen-film chest radiographs

Radiology, 1998-12, Vol.209 (3), p.705

1998

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CT of the pulmonary nodule: a cooperative study

Radiology, 1986-08, Vol.160 (2), p.319

1986

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Spiral CT: decreased spatial resolution in vivo due to broadening of section-sensitivity profile

Radiology, 1992-11, Vol.185 (2), p.469

1992

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Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis

American journal of respiratory and critical care medicine, 2014-07, Vol.190 (2), p.175-184

2014

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590 Changing face of pediatric pulmonary exacerbations in cystic fibrosis

Journal of cystic fibrosis, 2023-10, Vol.22, p.S313-S313

2023

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Neonatal Hirschsprung disease, dysautonomia, and central hypoventilation

Obstetrics and gynecology (New York. 1953), 1999-05, Vol.93 (5), p.834-836

1999

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Monitoring inflammation in CF. Cytokines

Clinical reviews in allergy & immunology, 2002-08, Vol.23 (1), p.41-57

2002

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B83 PEDIATRIC CLINICAL CHEST ROUNDS: Nno Clear Etiology: Bronchiectasis In A Native American Male

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

2016

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C67 SUPPURATIVE LUNG DISEASES IN CHILDREN: Cytoplasmic Ciliary Inclusions In Isolation Are Not Sufficient For The Diagnosis Of Primary Ciliary Dyskinesia In Children

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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Long term clinical effectiveness of ivacaftor in people with the G551D CFTR mutation

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

Dynamic incremental CT: effect of volume and concentration of contrast material and patient weight on hepatic enhancement

Blood mRNA biomarkers for detection of treatment response in acute pulmonary exacerbations of cystic fibrosis

Hepatic spiral CT: reduction of dose of intravenous contrast material

Dynamic contrast-enhanced CT of the liver: comparison of contrast medium injection rates and uniphasic and biphasic injection protocols

730 Longitudinal impact of pulmonary exacerbation frequency on lung function in children with cystic fibrosis

139 Discovering symptom clustering patters during a pulmonary exacerbation in people with cystic fibrosis

512 Hepatic and nutritional outcomes of Hispanic and non-Hispanic children with cystic fibrosis

12 Using continuous glucose monitoring to predict disease progression and development of diabetes in youth with cystic fibrosis

557 Relationship between metabolomic profiles and clinical outcomes after CFTR rescue

C67 SUPPURATIVE LUNG DISEASES IN CHILDREN: Automated Airway Scores Of Bronchiectasis In Children With Cystic Fibrosis Using A Machine Learning Classifier

578: Serum biomarkers identified by proteomics and measured by commercially available assays associated with lung function during clinically stable states

693 Improving timeliness and equity of cystic fibrosis newborn screening in Colorado and Wyoming

Detection of CT-proved pulmonary nodules: comparison of selenium-based digital and conventional screen-film chest radiographs

CT of the pulmonary nodule: a cooperative study

Spiral CT: decreased spatial resolution in vivo due to broadening of section-sensitivity profile

Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis

590 Changing face of pediatric pulmonary exacerbations in cystic fibrosis

Neonatal Hirschsprung disease, dysautonomia, and central hypoventilation

Monitoring inflammation in CF. Cytokines

B83 PEDIATRIC CLINICAL CHEST ROUNDS: Nno Clear Etiology: Bronchiectasis In A Native American Male

C67 SUPPURATIVE LUNG DISEASES IN CHILDREN: Cytoplasmic Ciliary Inclusions In Isolation Are Not Sufficient For The Diagnosis Of Primary Ciliary Dyskinesia In Children

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