S. Davis

发表

An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children.

Janet Stocks, Zoltán Hantos, Hans Bisgaard, 2007, American journal of respiratory and critical care medicine.

Progression of Lung Disease in Preschool Patients with Cystic Fibrosis

S. Stanojevic, F. Ratjen, P. Subbarao, 2017, American journal of respiratory and critical care medicine.

Neonatal and pediatric respiratory diagnostics.

S. Davis, 2003, Respiratory care.

Analysis of the associations between lung function and clinical features in preschool children with Cystic Fibrosis

M. Rosenfeld, R. Castile, P. Jones, 2012, Pediatric pulmonology.

Fractional Exhaled Nitric Oxide: Indications and Interpretation

S. Davis, C. Kercsmar, Young-Jee Kim, 2015 .

Inhaled hypertonic saline in preschool children with cystic fibrosis (SHIP): a multicentre, randomised, double-blind, placebo-controlled trial.

S. Stanojevic, R. Kronmal, M. Rosenfeld, 2019, The Lancet. Respiratory medicine.

Improving complex medical care while awaiting next‐generation CFTR potentiators and correctors: The current pipeline of therapeutics

S. Davis, J. Goralski, 2015, Pediatric pulmonology.

Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease.

L. A. Daniels, M. Knowles, M. Zariwala, 2013, American journal of respiratory and critical care medicine.

Update of respiratory tract disease in children with primary ciliary dyskinesia.

S. Dell, S. Sagel, S. Davis, 2011, Proceedings of the American Thoracic Society.

Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline

M. Rosenfeld, S. Daniel, Marcus H. Jones, 2018, American journal of respiratory and critical care medicine.

Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents.

M. Rosenfeld, J. Krischer, Hye-Seung Lee, 2016, Annals of the American Thoracic Society.

Nasal Nitric Oxide and Ciliary Videomicroscopy: Tests Used for Diagnosing Primary Ciliary Dyskinesia

M. Leigh, A. Shapiro, M. Chilvers, 2015 .

Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

M. Rosenfeld, M. Hazucha, J. Carson, 2014, Chest.

Founder Mutation in RSPH4A Identified in Patients of Hispanic Descent with Primary Ciliary Dyskinesia

F. Collins, M. Hazucha, J. Carson, 2013, Human mutation.

Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.

M. Rosenfeld, J. Krischer, Hye-Seung Lee, 2013, Annals of the American Thoracic Society.

Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: A multicenter experience

M. Rosenfeld, J. Carson, T. Ferkol, 2011, Pediatric pulmonology.

Respiratory consequences of prematurity: evolution of a diagnosis and development of a comprehensive approach

J. Ellenberg, A. Hamvas, G. Pryhuber, 2015, Journal of Perinatology.

Official American Thoracic Society Clinical Practice Guidelines: Diagnostic Evaluation of Infants with Recurrent or Persistent Wheezing.

J. Brożek, M. Sockrider, M. Durand, 2016, American journal of respiratory and critical care medicine.

Pediatric pulmonology year in review 2014: Part 2

R. Auten, T. Noah, J. Schwarze, 2015, Pediatric pulmonology.

Cystic Fibrosis Foundation practice guidelines for the management of infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome during the first two years of life and beyond.

M. Rosenfeld, R. Parad, F. Accurso, 2009, The Journal of pediatrics.

Azithromycin for Early Pseudomonas Infection in Cystic Fibrosis. The OPTIMIZE Randomized Trial

M. Rosenfeld, G. Kerby, F. Accurso, 2018, American journal of respiratory and critical care medicine.

Novel Outcome Measures for Clinical Trials in Cystic Fibrosis

H. Tiddens, D. Waltz, S. Donaldson, 2014, Pediatric pulmonology.

Effect of continuous positive airway pressure on forced expiratory flows in infants with tracheomalacia.

R. Tepper, C. Angelicchio, J. Kisling, 1998, American journal of respiratory and critical care medicine.

Outcomes of Children With Severe Bronchopulmonary Dysplasia Who Were Ventilator Dependent at Home

A. Carroll, A. Cristea, N. Swigonski, 2013, Pediatrics.

Unexplained Practice Variation in Primary Care Providers' Concern for Pediatric Obstructive Sleep Apnea.

S. Downs, T. Dugan, C. Saha, 2018, Academic pediatrics.

Preschool Multiple‐Breath Washout Testing. An Official American Thoracic Society Technical Statement

S. Stanojevic, M. Rosenfeld, M. Gappa, 2018, American journal of respiratory and critical care medicine.

Preschool Multiple-Breath Washout Testing

S. Stanojevic, M. Rosenfeld, M. Gappa, 2018 .

Cystic fibrosis: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.

G. Cutting, T. Ferkol, R. Boucher, 2014, Annals of the American Thoracic Society.

Innovating and adapting in pediatric pulmonology and sleep medicine during the COVID‐19 pandemic: ATS pediatric assembly web committee consensus statement for initial COVID‐19 virtual response

M. Rosenfeld, D. Ingram, R. Deterding, 2020, Pediatric pulmonology.

Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia.

Emily H Turner, J. Shendure, D. Nickerson, 2013, American journal of human genetics.

Spirometry centile charts for young Caucasian children: the Asthma UK Collaborative Initiative.

S. Stanojevic, A. Wade, J. Stocks, 2009, American journal of respiratory and critical care medicine.

Increased microbiota diversity associated with higher FEV0.5 in infants

D. Rusch, J. Slaven, K. Kloepfer, 2020, Pediatric pulmonology.

Physiologic, bronchoscopic, and bronchoalveolar lavage fluid findings in young children with recurrent wheeze and cough

W. T. Harris, T. Noah, J. Gelfond, 2006, Pediatric pulmonology.

Breathing easier: addressing the challenges of aerosolizing medications to infants and preschoolers.

S. Davis, J. Goralski, 2014, Respiratory medicine.

Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis

W. T. Harris, T. Noah, R. Goel, 2009, Pediatric pulmonology.

Early lung disease in young children with primary ciliary dyskinesia

M. Leigh, S. Davis, J. Pittman, 2008, Pediatric pulmonology.

An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia

E. Kilbride, T. Ferkol, P. Latzin, 2022, ERJ Open Research.

Limitations of Nasal Nitric Oxide Testing in Primary Ciliary Dyskinesia

T. Ferkol, M. Knowles, M. Leigh, 2020, American journal of respiratory and critical care medicine.

A comparison of nasal nitric oxide measurement modes

M. Hazucha, A. Shapiro, S. Davis, 2017, Pediatric pulmonology.

Inhaled hypertonic saline in infants and toddlers with cystic fibrosis: short‐term tolerability, adherence, and safety

M. Rosenfeld, S. Daniel, F. Ratjen, 2011, Pediatric pulmonology.

Ventilation Heterogeneity and Airway Hyperreactivity in Children with Well Controlled Asthma

C. Tiller, R. Tepper, J. Kisling, 2016 .

Identifying the origins of cystic fibrosis lung disease.

T. Ferkol, S. Davis, 2013, The New England journal of medicine.

Evaluation of clinically relevant changes in the lung clearance index in children with cystic fibrosis and healthy controls

S. Stanojevic, D. Sanders, V. Waters, 2022, Thorax.

Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls.

M. Rosenfeld, W. Wheeler, A. Griffiths, 2020, Annals of the American Thoracic Society.

Cystic fibrosis in El Salvador

D. Sanders, J. Slaven, J. Stevens, 2019, Pediatric pulmonology.

Reference equations for the interpretation of forced expiratory and plethysmographic measurements in infants

M. Sears, F. Ratjen, T. Moraes, 2018, Pediatric pulmonology.

Lung clearance index to monitor treatment response in pulmonary exacerbations in preschool children with cystic fibrosis

S. Stanojevic, F. Ratjen, G. Retsch-Bogart, 2018, Thorax.

Preterm respiratory disease in the modern era: the value of cohort studies

S. Davis, G. Montgomery, 2017, Thorax.

Glutathione‐S‐transferase P1 may predispose children to a decline in pulmonary function after stem cell transplant

Zhangsheng Yu, J. Slaven, J. Stark, 2017, Pediatric pulmonology.

Glutathione-S-transferase P 1 may predispose children to a decline in pulmonary function after stem cell transplant

Zhangsheng Yu, J. Slaven, J. Stark, 2017 .

Decline in Forced Expiratory Volume in 1 Second in Cystic Fibrosis--Watch the Pendulum Swing.

S. Davis, J. Pittman, 2016, The Journal of pediatrics.

Bronchodilator responsiveness in normal infants and young children.

R. Castile, K. McCoy, R. Tepper, 2001, American journal of respiratory and critical care medicine.

Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial.

P. Lee, J. Elborn, J. Davies, 2013, The Lancet. Respiratory medicine.

Challenges and limitations of testing efficacy of aerosol device delivery in young children.

S. Davis, J. Goralski, 2014, Journal of aerosol medicine and pulmonary drug delivery.

Association of lung function, chest radiographs and clinical features in infants with cystic fibrosis

M. Rosenfeld, R. Castile, G. Kerby, 2013, European Respiratory Journal.

Early respiratory viral infections in infants with cystic fibrosis

S. Stick, G. Storch, T. Ferkol, 2019, Journal of Cystic Fibrosis.

The effect of inhaled hypertonic saline on lung structure in children aged 3-6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial.

R. Kronmal, M. Rosenfeld, E. Andrinopoulou, 2022, The Lancet. Respiratory medicine.

Lung clearance index in children with sickle cell disease

J. Slaven, S. Peterson-Carmichael, S. Davis, 2020, Pediatric pulmonology.

Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline.

S. Stanojevic, M. Rosenfeld, F. Ratjen, 2013, American journal of respiratory and critical care medicine.

Emerging Genotype-Phenotype Relationships in Primary Ciliary Dyskinesia

T. Ferkol, S. Davis, S. Brennan, 2021, International journal of molecular sciences.

Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: A multicenter experience

M. Rosenfeld, J. Carson, T. Ferkol, 2009, Pediatric pulmonology.

Comparison of normal infants and infants with cystic fibrosis using forced expiratory flows breathing air and heliox *

R. Tepper, J. Kisling, S. Davis, 2001, Pediatric pulmonology.

A four week trial of hypertonic saline in children with mild cystic fibrosis lung disease: Effect on mucociliary clearance and clinical outcomes.

A. Ceppe, S. Donaldson, W. Bennett, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Treatment recommendations in Primary Ciliary Dyskinesia.

S. Dell, D. Polineni, S. Davis, 2016, Paediatric respiratory reviews.

Exhaled breath condensate purines correlate with lung function in infants and preschoolers

S. Davis, C. Esther, Robin C. Johnson, 2011, Pediatric pulmonology.

The utility of moment ratios and abbreviated endpoints of the multiple breath washout test in preschool children with cystic fibrosis

S. Stanojevic, F. Ratjen, G. Retsch-Bogart, 2020, Pediatric pulmonology.

Multiple‐Breath Washout Outcomes Are Sensitive to Inflammation and Infection in Children with Cystic Fibrosis

S. Stick, K. Ramsey, B. Skoric, 2017, Annals of the American Thoracic Society.

Multiple-BreathWashout Outcomes Are Sensitive to In fl ammation and Infection in Children with Cystic Fibrosis

S. Stick, K. Ramsey, B. Skoric, 2017 .

Tracking pulmonary exacerbations in preschool children using the lung clearance index

S. Stanojevic, F. Ratjen, P. Subbarao, 2016 .

Eosinophilic esophagitis in cystic fibrosis: a case series and review of the literature.

Daniel M. Lercher, E. Dellon, S. Davis, 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Safety and tolerability of inhaled hypertonic saline in young children with cystic fibrosis

S. Donaldson, S. Davis, E. Dellon, 2008, Pediatric pulmonology.

Spirometry in biracial children: how adequate are race-based reference equations?

A. Van Rie, S. Davis, J. Pittman, 2011, Archives of pediatrics & adolescent medicine.

Hyperinflation is associated with increased respiratory rate and is a more sensitive measure of cystic fibrosis lung disease during infancy compared to forced expiratory measures

T. Ferkol, J. Slaven, C. Tiller, 2020, Pediatric pulmonology.

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

M. Rosenfeld, G. Kerby, S. Donaldson, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

INHALED HYPERTONIC SALINE IN INFANTS AND CHILDREN LESS THAN SIX YEARS OF AGE WITH CYSTIC FIBROSIS: THE ISIS RANDOMIZED TRIAL

R. Kronmal, M. Rosenfeld, S. Daniel, 2013 .

Improvement in pulmonary function following antibiotics in infants with cystic fibrosis

S. Davis, J. Pittman, Robin C. Johnson, 2012, Pediatric pulmonology.

Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype.

M. Rosenfeld, J. Krischer, Hye-Seung Lee, 2015, American journal of respiratory and critical care medicine.

High-Speed Videomicroscopy Analysis Presents Limitations in Diagnosis of Primary Ciliary Dyskinesia

T. Ferkol, M. Knowles, M. Leigh, 2020, American journal of respiratory and critical care medicine.

The Diagnostic Dilemma Of Primary Ciliary Dyskinesia: Findings And Experience Of The Genetic Disorders Of Mucociliary Clearance Consortium

M. Rosenfeld, J. Carson, T. Ferkol, 2011, ATS 2011.

Lung function distinguishes preschool children with CF from healthy controls in a multi‐center setting

M. Rosenfeld, R. Castile, P. Jones, 2012, Pediatric pulmonology.

Sensitivity of spirometric measurements to detect airway obstruction in infants.

Marcus H. Jones, R. Tepper, J. Kisling, 2003, American journal of respiratory and critical care medicine.

Rate constant for forced expiration decreases with lung growth during infancy.

R. Castile, R. Tepper, J. Kisling, 1999, American journal of respiratory and critical care medicine.

Building a pediatric rare lung disease program: It takes a community of villages

T. Vece, S. Davis, Miriam Davis, 2022, Pediatric pulmonology.

Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection

M. Drumm, Hannah Noah, M. Knowles, 2017, PloS one.

Infant pulmonary function testing: overview of technology and practical considerations--new current procedural terminology codes effective 2010.

B. Lesnick, S. Davis, 2011, Chest.

Nasal Nitric Oxide And Clinical Characteristics Of Patients With Heterotaxy: Comparison To Primary Ciliary Dyskinesia

B. Baker, M. Knowles, M. Leigh, 2011, ATS 2011.

Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype

M. Rosenfeld, J. Krischer, Hye-Seung Lee, 2019, American journal of respiratory and critical care medicine.

Basic primer for finances in academic adult and pediatric pulmonary divisions.

M. Steiner, L. Schnapp, S. Davis, 2020, Chest.

Definition Of Clinical Criteria For Diagnosis Of Primary Ciliary Dyskinesia

M. Rosenfeld, J. Krischer, Hye-Seung Lee, 2012, ATS 2012.

Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?

S. Matecki, P. Reix, L. Kent, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A 2-year-old girl with co-inherited cystic fibrosis and sickle cell-β+ thalassemia presenting with recurrent vaso-occlusive events during cystic fibrosis pulmonary exacerbations: a case report

C. Thornburg, J. Voynow, S. Peterson-Carmichael, 2013, Journal of Medical Case Reports.

Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review

M. Rosenfeld, S. Daniel, A. Kimple, 2015, Pediatric pulmonology.

Accuracy of Nasal Nitric Oxide Measurement as a Diagnostic Test for Primary Ciliary Dyskinesia. A Systematic Review and Meta‐analysis

M. Rosenfeld, M. Leigh, A. Shapiro, 2017, Annals of the American Thoracic Society.

Early Elevation of Plasma Periostin Is Associated with Chronic Ventilator-Dependent Bronchopulmonary Dysplasia.

B. Poindexter, S. Ahlfeld, S. Davis, 2016, American journal of respiratory and critical care medicine.

Use caution interpreting nasal nitric oxide: Overlap in primary ciliary dyskinesia and primary immunodeficiency

M. Knowles, M. Zariwala, M. Leigh, 2021, Pediatric pulmonology.

Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.

J. Shendure, D. Nickerson, M. Rosenfeld, 2014, American journal of respiratory and critical care medicine.

Primary ciliary dyskinesia in the genomics age.

H. Omran, A. Shoemark, S. Davis, 2020, The Lancet. Respiratory medicine.

Clinical Symptoms Associated With Primary Ciliary Dyskinesia : Results Of A Multi-Centered Study

M. Rosenfeld, T. Ferkol, C. Milla, 2010, ATS 2010.

A Multi-Center, Longitudinal Study Of Nasal Nitric Oxide In Children With Primary Ciliary Dyskinesia

M. Rosenfeld, M. Hazucha, T. Ferkol, 2010, ATS 2010.

Characteristics Of Primary Ciliary Dyskinesia In Children Under 5 Years Of Age

M. Rosenfeld, P. Jones, T. Ferkol, 2011, ATS 2011.

Age of Pseudomonas aeruginosa acquisition and subsequent severity of cystic fibrosis lung disease

M. Drumm, M. Emond, M. Knowles, 2011, Pediatric pulmonology.

Inhaled Hypertonic Saline in Infants and Children Younger Than 6 Years With Cystic Fibrosis (ISIS): The Randomized Controlled Trial

R. Kronmal, M. Rosenfeld, S. Daniel, 2013 .

Reduced lung function in cystic fibrosis: a primary or secondary phenotype?

F. Ratjen, S. Davis, 2008, American journal of respiratory and critical care medicine.

Pulmonary exacerbations and parent‐reported outcomes in children <6 years with cystic fibrosis

M. Rosenfeld, A. Quittner, S. Daniel, 2015, Pediatric pulmonology.

Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome

J. Carson, T. Ferkol, M. Knowles, 2009, Genetics in Medicine.

Official American Thoracic Society technical standards: flexible airway endoscopy in children.

G. Visner, T. Ferkol, T. Kilbaugh, 2015, American journal of respiratory and critical care medicine.

Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.

Emily H Turner, J. Shendure, D. Nickerson, 2013, American journal of human genetics.

Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

M. Rosenfeld, H. Omran, M. Hazucha, 2011, Thorax.

Proton Pump Inhibitors Are Associated with Reduced Incidence of Dysplasia in Barrett's Esophagus

A. Bhattacharyya, R. Sampliner, H. El‐Serag, 2004, American Journal of Gastroenterology.

De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.

H. Omran, A. Brentrup, S. Dutcher, 2019, American journal of human genetics.

Clinical Practice Guidelines From the Cystic Fibrosis Foundation for Preschoolers With Cystic Fibrosis

M. Rosenfeld, S. Powers, S. Schwarzenberg, 2016, Pediatrics.

Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis.

M. Rosenfeld, R. Parad, F. Accurso, 2009, The Journal of pediatrics.

Lung function from infancy to preschool in a cohort of children with cystic fibrosis

M. Rosenfeld, R. Castile, G. Kerby, 2012, European Respiratory Journal.

Multifaceted quality improvement initiative to decrease pediatric asthma readmissions

A. Cristea, S. Davis, Nadia L Krupp, 2017, The Journal of asthma : official journal of the Association for the Care of Asthma.

An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age.

J. Stocks, M. Rosenfeld, E. Oostveen, 2013, Annals of the American Thoracic Society.

MARCKS Is Marked in Combating Lung Cancer Growth and Acquired Resistance

J. Carlin, R. Castile, G. Kerby, 2014 .

Forced expiratory flows and volumes in infants. Normative data and lung growth.

W. Ambrosius, R. Castile, C. Emsley, 2000, American journal of respiratory and critical care medicine.

Forced expiratory maneuvers in very young children. Assessment of flow limitation.

R. Tepper, D. Grant, K. Christoph, 1999, American journal of respiratory and critical care medicine.

Care of the child with a chronic tracheostomy. This official statement of the American Thoracic Society was adopted by the ATS Board of Directors, July 1999.

R. Chatburn, R. Wood, C. Myer, 2000, American journal of respiratory and critical care medicine.

Use of polysomnography to assess safe decannulation in children

A. Cristea, J. Slaven, D. Givan, 2016, Pediatric pulmonology.

Retrospective Analysis of Factors Leading to Pediatric Tracheostomy Decannulation Failure. A Single‐Institution Experience

J. Slaven, D. Givan, S. Davis, 2017, Annals of the American Thoracic Society.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

M. Rosenfeld, H. Omran, T. Hurd, 2013, American journal of human genetics.

Bronchopulmonary Dysplasia: Executive Summary of a Workshop

T. Raju, N. Finer, R. Higgins, 2018, The Journal of pediatrics.

Prematurity and respiratory outcomes program (PROP): study protocol of a prospective multicenter study of respiratory outcomes of preterm infants in the United States

T. Mariani, D. Cifelli, J. Ellenberg, 2015, BMC Pediatrics.

Median Household Income: Association with Mortality in Children on Chronic Ventilation at Home Secondary to Bronchopulmonary Dysplasia.

A. Carroll, S. Downs, A. Cristea, 2015, Pediatric allergy, immunology, and pulmonology.

The clinical utility of lung clearance index in early cystic fibrosis lung disease is not impacted by the number of multiple-breath washout trials

K. Ramsey, B. Skoric, G. Hall, 2018, ERJ Open Research.

Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report.

Margaret Rosenfeld, Paul Aurora, Carlos Milla, 2015, Annals of the American Thoracic Society.

Characterization of Relations Among Sleep, Inflammation, and Psychiatric Dysfunction in Depressed Youth With Crohn Disease

Daniel J Buysse, D. Kupfer, A. Bousvaros, 2013, Journal of pediatric gastroenterology and nutrition.

A proposal for the addressing the needs of the pediatric pulmonary work force

D. Cornfield, J. Celedón, D. Gozal, 2020, Pediatric pulmonology.

Urine gastrin‐releasing peptide in the first week correlates with bronchopulmonary dysplasia and post‐prematurity respiratory disease

B. Poindexter, A. Herring, A. Hamvas, 2020, Pediatric pulmonology.

Lung Clearance Index to Track Acute Respiratory Events in School-age Children with Cystic Fibrosis.

S. Stanojevic, D. Sanders, V. Waters, 2020, American journal of respiratory and critical care medicine.

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

R. Kronmal, M. Rosenfeld, Robin Johnson, 2012, JAMA.

Association between early respiratory viral infections and structural lung disease in infants with cystic fibrosis.

D. Sanders, H. Tiddens, S. Stick, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Association of Antibiotics, Airway Microbiome, and Inflammation in Infants with Cystic Fibrosis

K. Wylie, S. Stick, G. Storch, 2017, Annals of the American Thoracic Society.

Changes in the parent cystic fibrosis questionnaire-revised (CFQ-R) with respiratory symptoms in preschool children with cystic fibrosis.

S. Stanojevic, F. Ratjen, G. Retsch-Bogart, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Initial evaluation of the Parent Cystic Fibrosis Questionnaire--Revised (CFQ-R) in infants and young children.

M. Rosenfeld, A. Quittner, F. Ratjen, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Endpoints for clinical trials in young children with cystic fibrosis.

M. Rosenfeld, M. Emond, L. Brumback, 2007, Proceedings of the American Thoracic Society.

Addressing Gender Inequality in Our Disciplines: Report from the Association of Pulmonary, Critical Care, and Sleep Division Chiefs

C. Bates, C. Thomson, L. Tanoue, 2018, Annals of the American Thoracic Society.

The future of pediatric pulmonology: A survey of division directors, assessment of current research funding, and discussion of workforce trends

T. Noah, P. Moore, S. Peterson-Carmichael, 2020, Pediatric pulmonology.

Polysomnography Reference Values in Healthy Newborns.

J. Slaven, S. Davis, A. Daftary, 2019, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

PEDIATRIC PULMONOLOGY

D. Rusch, K. Kloepfer, S. Davis, 2019 .

Diagnostic Modalities: Pulmonary Function Testing and Imaging

A. Cristea, S. Davis, C. Ren, 2017 .

In children, the microbiota of the nasopharynx and bronchoalveolar lavage fluid are both similar and different

D. Rusch, K. Kloepfer, S. Peterson-Carmichael, 2018, Pediatric pulmonology.

Sleep and pulmonary outcomes for clinical trials of airway plexiform neurofibromas in NF1

C. Marcus, B. Widemann, R. Ferner, 2016, Neurology.

intestinein the submucosal plexus of guinea pig small Stimulation of adenosine A1 and A2A receptors by

Hongzhen Hu, N. Alexis, S. Vanner, 2011 .

Inter-test reproducibility of the lung clearance index measured by multiple breath washout

S. Stanojevic, F. Ratjen, G. Retsch-Bogart, 2017, European Respiratory Journal.

Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial.

R. Kronmal, M. Rosenfeld, E. Andrinopoulou, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Multi-modality monitoring of cystic fibrosis lung disease: the role of chest computed tomography.

H. Tiddens, S. Stick, S. Davis, 2014, Paediatric respiratory reviews.

Comparative analysis of respiratory symptom scores to detect acute respiratory events in children with cystic fibrosis.

S. Stanojevic, D. Sanders, V. Waters, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pulmonary function tests in extremely low gestational age infants at one year of age

E. Eichenwald, A. Dylag, J. Voynow, 2021, Pediatric pulmonology.

Pulmonary Morbidity in Infancy after Exposure to Chorioamnionitis in Late Preterm Infants.

A. Jobe, C. Chougnet, W. Hardie, 2016, Annals of the American Thoracic Society.

Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints.

M. Rosenfeld, R. Castile, G. Kerby, 2010, American journal of respiratory and critical care medicine.

Differences in the lower airway microbiota of infants with and without cystic fibrosis.

K. Wylie, G. Storch, T. Ferkol, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Physiologic findings in children previously ventilator dependent at home due to bronchopulmonary dysplasia

A. Cristea, Zhangsheng Yu, J. Slaven, 2015, Pediatric pulmonology.

Early Neonatal Oxygen Exposure Predicts Pulmonary Morbidity and Functional Deficits at 1 Year.

M. O’Reilly, G. Pryhuber, Hongyue Wang, 2020, The Journal of pediatrics.

Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis.

B. Yankaskas, B. Qaqish, T. Noah, 2007, American journal of respiratory and critical care medicine.

Density dependence of forced expiratory flows in healthy infants and toddlers.

R. Castile, R. Tepper, J. Kisling, 1999, Journal of applied physiology.

Flow limitation in infants assessed by negative expiratory pressure.

R. Castile, R. Tepper, J. Kisling, 2000, American Journal of Respiratory and Critical Care Medicine.

Survey of clinical infant lung function testing practices

M. Rosenfeld, C. Hornik, G. Hall, 2014, Pediatric pulmonology.

12 – Pulmonary Function Testing in Children

R. Castile, S. Davis, 2012 .

Pediatric Pulmonology year in review 2015: Part 1

R. Auten, T. Noah, J. Schwarze, 2016, Pediatric pulmonology.

Hitting the target: new treatments for cystic fibrosis.

T. Ferkol, Thomas W Ferkol, S. Davis, 2010, American journal of respiratory and critical care medicine.

American Thoracic Society Documents An Official American Thoracic Society/European Respiratory Society Statement: Pulmonary Function Testing in Preschool Children

M. G. Morris, J. Stocks, M. Silverman, 2007 .

Airway Inflammation in Children with Primary Ciliary Dyskinesia.

M. Rosenfeld, H. Tiddens, T. Ferkol, 2022, Annals of the American Thoracic Society.

Safety of intravenous tobramycin in combination with a variety of anti-pseudomonal antibiotics in children with cystic fibrosis

J. Slaven, S. Davis, R. Pettit, 2017, SAGE Open Medicine.

Extracellular purines are biomarkers of neutrophilic airway inflammation

N. Alexis, S. Donaldson, E. Lazarowski, 2008, European Respiratory Journal.

Table of Contents

G. Pryhuber, Hongyue Wang, A. Dylag, 2020, The Journal of Pediatrics.

Ability of the lung clearance index to monitor progression of early lung disease in children with cystic fibrosis

S. Stick, K. Ramsey, B. Skoric, 2016 .

Variability of a closed, rebreathing setup for multiple breath wash‐out testing in children

S. Davis, J. Pittman, Robin C. Johnson, 2012, Pediatric pulmonology.

Monitoring of Structure and Function in Early Cystic Fibrosis Lung Disease.

M. Rosenfeld, S. Ranganathan, S. Davis, 2011, Pediatric allergy, immunology, and pulmonology.

Quality Control for Spirometry in Preschool Children

H. Eigen, N. Beydon, S. Davis, 2008 .

Tidal Breathing Measurements at Discharge and Clinical Outcomes in Extremely Low Gestational Age Neonates

E. Eichenwald, A. Jobe, P. Moore, 2018, Annals of the American Thoracic Society.

Official American Thoracic Society Clinical Practice Guidelines: Diagnostic Evaluation of Infants with Recurrent or Persistent Wheezing.

J. Brożek, M. Sockrider, M. Durand, 2016, American journal of respiratory and critical care medicine.

Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

M. Rosenfeld, M. Hazucha, J. Carson, 2014, Chest.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

M. Rosenfeld, H. Omran, T. Hurd, 2013, American journal of human genetics.

Determinants of lung disease progression measured by lung clearance index in children with cystic fibrosis

S. Stanojevic, D. Sanders, V. Waters, 2021, European Respiratory Journal.

NHLBI WORKSHOP Cystic Fibrosis: NHLBIWorkshop on the Primary Prevention of Chronic Lung Diseases

G. Cutting, T. Ferkol, R. Boucher, 2014 .

Spirometry in biracial children: how adequate are race-based reference equations?

A. Van Rie, S. Davis, J. Pittman, 2011, Archives of pediatrics & adolescent medicine.

Reversal of Irritable Bowel Syndrome, Sleep Disturbance, and Fatigue With an Elimination Diet, Lifestyle Modification, and Dietary Supplements: A Case Report.

S. Davis, 2016, Integrative medicine.

M. Rosenfeld, R. Parad, F. Accurso, 2009, The Journal of pediatrics.

Pediatric Pulmonology year in review 2015: Part 1

T. Nicolai, R. Auten, T. Noah, 2016, Pediatric pulmonology.

Clinical Practice Guidelines From the Cystic Fibrosis Foundation for Preschoolers With Cystic Fibrosis

M. Rosenfeld, S. Powers, R. P. Guillerman, 2016, Pediatrics.

Preterm respiratory disease in the modern era: the value of cohort studies

S. Davis, G. Montgomery, 2017, Thorax.

Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline

M. Rosenfeld, S. Daniel, Marcus H. Jones, 2018, American Journal of Respiratory and Critical Care Medicine.

Nasal nitric oxide measurement in children for the diagnosis of primary ciliary dyskinesia: European Respiratory Society technical standard

E. Kilbride, T. Ferkol, P. Latzin, 2023, European Respiratory Journal.