K. McCoy

发表

Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis *

J. Emerson, R. Gibson, M. Rosenfeld, 2001, Pediatric pulmonology.

The role of computerized order sets in pediatric inpatient asthma treatment

A. McAlearney, K. McCoy, D. Chisolm, 2006, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Diagnostic accuracy of oropharyngeal cultures in infants and young children with cystic fibrosis

J. Emerson, M. Rosenfeld, R. Castile, 1999, Pediatric pulmonology.

Environmental exposures and family history of asthma

K. McCoy, N. Ryan-Wenger, J. Pitts, 2016, The Journal of asthma : official journal of the Association for the Care of Asthma.

Eucapnic Voluntary Hyperventilation to Detect Exercise-Induced Bronchoconstriction in Cystic Fibrosis

K. McCoy, C. E. Wisely, Jonathan P. Parsons, 2015, Lung.

Pseudomonas aeruginosa antibiotic susceptibility during long-term use of aztreonam for inhalation solution (AZLI).

R. Gibson, K. McCoy, C. Oermann, 2011, The Journal of antimicrobial chemotherapy.

An 18‐month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in cystic fibrosis

R. Gibson, A. Quittner, K. McCoy, 2010, Pediatric pulmonology.

Update on antibiotics for infection control in cystic fibrosis

K. McCoy, S. Kirkby, K. Novak, 2009, Expert review of anti-infective therapy.

Efficacy and safety of inhaled aztreonam lysine for airway pseudomonas in cystic fibrosis.

R. Gibson, A. Quittner, K. McCoy, 2009, Chest.

Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis.

R. Gibson, A. Quittner, K. McCoy, 2008, American journal of respiratory and critical care medicine.

Effects of 12-Week Administration of Dornase Alfa in Patients with Advanced Cystic Fibrosis Lung Disease

Charles A. Johnson, K. McCoy, S. Hamilton, 1996 .

Effects of 12-week administration of dornase alfa in patients with advanced cystic fibrosis lung disease. Pulmozyme Study Group.

K. McCoy, C. Johnson, S. Hamilton, 1996, Chest.

A phase 2 study of aztreonam lysine for inhalation to treat patients with cystic fibrosis and Pseudomonas aeruginosa infection

R. Gibson, T. Liou, J. Burns, 2008, Pediatric pulmonology.

Dysregulated Calcium Homeostasis in Cystic Fibrosis Neutrophils Leads to Deficient Antimicrobial Responses

L. Bakaletz, K. McCoy, A. Amer, 2018, The Journal of Immunology.

How reliable is a radiological report in osteoporosis in diagnosing low bone density?

K. McCoy, C. D. McCullagh, V. Crawford, 2003, The Ulster medical journal.

Demographics, Clinical Course, and Outcomes of Children with Status Asthmaticus Treated in a Pediatric Intensive Care Unit: 8-Year Review

K. McCoy, N. Ryan-Wenger, S. Sheikh, 2013, The Journal of asthma : official journal of the Association for the Care of Asthma.

Mycobacterium abscessus Smooth and Rough Morphotypes Form Antimicrobial-Tolerant Biofilm Phenotypes but Are Killed by Acetic Acid

A. Azad, K. McCoy, L. Schlesinger, 2018, Antimicrobial Agents and Chemotherapy.

Mucus plugging, air trapping, and bronchiectasis are important outcome measures in assessing progressive childhood cystic fibrosis lung disease

D. Cornfield, M. Goris, P. D. de Jong, 2020, Pediatric pulmonology.

Copper enzyme activities in cystic fibrosis before and after copper supplementation plus or minus zinc.

K. McCoy, R. DiSilvestro, K. Best, 2004, Metabolism: clinical and experimental.

Trends in Inhaled Antibiotic Therapy

K. McCoy, S. Sullivan, 2016 .

Urinary leukotriene E(4) excretion during the first month of life and subsequent bronchopulmonary dysplasia in premature infants.

K. McCoy, D. Gentile, David Skoner, 2001, Chest.

Developmental delays and pulmonary disease severity in cystic fibrosis.

K. McCoy, M. Mahaney, 1986, Human biology.

Resolution of cystic fibrosis-related diabetes with ivacaftor therapy.

K. McCoy, D. Hayes, S. Sheikh, 2014, American journal of respiratory and critical care medicine.

Improvement of sinus disease in cystic fibrosis with ivacaftor therapy.

K. McCoy, D. Hayes, S. Sheikh, 2014, American journal of respiratory and critical care medicine.

Gas trapping in normal infants and in infants with cystic fibrosis

R. Castile, K. McCoy, D. Iram, 2004, Pediatric pulmonology.

K. McCoy, L. Taussig, L. Landau, 1993, Pediatric pulmonology.

Can the histologic changes of cystic fibrosis-associated hepatobiliary disease be predicted by clinical criteria?

S. Qualman, K. McCoy, M. Fishbein, 1997, Journal of pediatric gastroenterology and nutrition.

Inpatient healthcare trends among adult cystic fibrosis patients in the U.S.

Deena J. Chisolm, K. Kelleher, K. McCoy, 2012, Pediatric pulmonology.

Healthy elderly individuals do not inevitably lose bone density and weight as they age.

D. Craig, K. McCoy, H. Taggart, 2004, Archives of gerontology and geriatrics.

Weighing in on asthma: Insights on BMI, magnesium, and hospitalizations from the Ohio Pediatric Asthma Repository

Lisa J. Martin, V. Pilipenko, G. K. Khurana Hershey, 2020, The Journal of asthma : official journal of the Association for the Care of Asthma.

Longitudinal assessment of Pseudomonas aeruginosa in young children with cystic fibrosis.

J. Emerson, R. Gibson, M. Rosenfeld, 2001, The Journal of infectious diseases.

Why doesn't reducing exacerbations decrease COPD mortality?

R. Gibson, K. McCoy, C. Oermann, 2014 .

Elevated Hepatic Glucose Production in Children with Cystic Fibrosis

K. McCoy, C. Horswill, C. L. Kien, 1995, Pediatric Research.

Biofilm aggregates and the host airway-microbial interface

K. McCoy, L. Hall-Stoodley, 2022, Frontiers in Cellular and Infection Microbiology.

Pharmacokinetics and safety of cavosonstat (N91115) in healthy and cystic fibrosis adults homozygous for F508DEL-CFTR.

S. Donaldson, P. Zeitlin, K. McCoy, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pulmonary hypertension in cystic fibrosis with advanced lung disease.

B. Whitson, J. Tobias, K. McCoy, 2014, American journal of respiratory and critical care medicine.

Screening high-risk children for asthma through a community intervention

K. McCoy, N. Ryan-Wenger, J. Pitts, 2015, The Journal of asthma : official journal of the Association for the Care of Asthma.

Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial

C. Teneback, P. Sosnay, R. Klingsberg, 2019, The Lancet.

Bronchodilator responsiveness in normal infants and young children.

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

Cystic fibrosis transmembrane conductance regulator modulators and the exocrine pancreas: A scoping review.

Vikesh K. Singh, P. Hart, Mitchell L. Ramsey, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Prolonged parenteral nutrition for cystic fibrosis patients.

K. McCoy, A. Mick, E. Allen, 1995, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.

Racial differences in pet ownership in families of children with asthma

K. McCoy, N. Ryan-Wenger, J. Pitts, 2016, World Journal of Pediatrics.

A comparison of the therapeutic effectiveness of and preference for postural drainage and percussion, intrapulmonary percussive ventilation, and high-frequency chest wall compression in hospitalized cystic fibrosis patients.

R. Castile, K. McCoy, D. Filbrun, 2003, Respiratory care.

Chapter 49 – Idiopathic Pulmonary Hemosiderosis

K. McCoy, S. Sheikh, 2008 .

Computed tomography correlates with improvement with ivacaftor in cystic fibrosis patients with G551D mutation.

K. McCoy, N. Ryan-Wenger, F. Long, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Ivacaftor improves appearance of sinus disease on computerised tomography in cystic fibrosis patients with G551D mutation

K. McCoy, N. Ryan-Wenger, F. Long, 2015, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.

CONTINUOUS VS. INTERMITTENT AEROSOLIZED ALBUTEROL IN THE TREATMENT OF ACUTE ASTHMA IN CHILDREN

K. McCoy, M. Hoppe, C. Standing, 1989 .

Changes in Pulmonary Function and Controlled Ventilation-High Resolution CT of Chest After Antibiotic Therapy in Infants and Young Children with Cystic Fibrosis

K. McCoy, N. Ryan-Wenger, F. Long, 2015, Lung.

Exaggerated inflammatory responses mediated by Burkholderia cenocepacia in human macrophages derived from Cystic fibrosis patients.

K. McCoy, A. Amer, B. Kopp, 2012, Biochemical and biophysical research communications.

Feeding-induced changes in energy expenditure in children with cystic fibrosis.

K. McCoy, C. Horswill, W. Zipf, 1994, JPEN. Journal of parenteral and enteral nutrition.

Assessing bronchodilator responsiveness in infants using partial expiratory flow‐volume curves

R. Castile, K. McCoy, J. Hayes, 2003, Pediatric pulmonology.

Molecular and Clinical Comparison of Enterovirus D68 Outbreaks among Hospitalized Children, Ohio, USA, 2014 and 2018

A. Mejias, K. McCoy, A. Leber, 2019, Emerging infectious diseases.

Aquagenic wrinkling in children under two years of age: Could this be a potential clinical referral tool for cystic fibrosis among non-screened populations?

K. McCoy, Shasha Bai, G. Paul, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Improved quality-of-life of caregivers of children with asthma through guideline-based management

K. McCoy, N. Ryan-Wenger, J. Pitts, 2017, The Journal of asthma : official journal of the Association for the Care of Asthma.

Right heart catheterization measuring central hemodynamics in cystic fibrosis during exercise.

K. McCoy, H. Mansour, C. Daniels, 2013, Respiratory medicine.

Predicting episodes of poor asthma control in treated patients with asthma.

David M. Shade, N. Anthonisen, M. Castro, 2006, The Journal of allergy and clinical immunology.

Effects of an Antioxidant‐enriched Multivitamin in Cystic Fibrosis. A Randomized, Controlled, Multicenter Clinical Trial

J. Clancy, K. McCoy, D. Orenstein, 2018, American journal of respiratory and critical care medicine.

Pharmacokinetics and safety of tobramycin after once-daily administration in patients with cystic fibrosis.

M. Nahata, K. McCoy, G. Young, 1997, Chest.

Incidence and prevalence of neutralizing antibodies to the common adenoviruses in children with cystic fibrosis: implication for gene therapy with adenovirus vectors.

B. Ramsey, P. Hiatt, K. McCoy, 1998, Pediatrics.

Tolerability and compliance with risedronate in clinical practice

K. McCoy, H. Taggart, B. Hamilton, 2003, Osteoporosis International.

Presentation of bronchial mucoepidermoid carcinoma as unilateral hyperlucent lung

K. McCoy, E. Allen, 1990, Pediatric pulmonology.

Papilloma of the ears of calves following tattooing.

K. McCoy, M. Studdert, M. Allworth, 1988, Australian veterinary journal.

Novel Computed Tomography Scoring System for Sinus Disease in Adults With Cystic Fibrosis

K. McCoy, N. Ryan-Wenger, D. Hayes, 2016, The Annals of otology, rhinology, and laryngology.

High‐risk age window for mortality in children with cystic fibrosis after lung transplantation

J. Tobias, K. McCoy, D. Hayes, 2015, Pediatric transplantation.

Targeting bacterial integration host factor to disrupt biofilms associated with cystic fibrosis.

S. Goodman, J. Jurcisek, L. Bakaletz, 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Autophagy stimulation by rapamycin suppresses lung inflammation and infection by Burkholderia cenocepacia in a model of cystic fibrosis

M. Valvano, K. McCoy, M. Wewers, 2011, Autophagy.

Burkholderia cenocepacia O polysaccharide chain contributes to caspase‐1‐dependent IL‐1β production in macrophages

C. Marsh, M. Valvano, K. McCoy, 2011, Journal of leukocyte biology.

Aztreonam (for inhalation solution) for the treatment of chronic lung infections in patients with cystic fibrosis: an evidence-based review

K. McCoy, S. Kirkby, K. Novak, 2011, Core evidence.

Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.

Xiaohong Huang, Michael P Boyle, Carla Colombo, 2015, The New England journal of medicine.

The expression of Mirc1/Mir17-92 cluster in sputum samples correlates with pulmonary exacerbations in cystic fibrosis patients.

N. Parinandi, K. McCoy, D. Tumin, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Lateral thoracic expansion for Jeune's asphyxiating dystrophy: a new approach.

K. McCoy, R. Ruberg, D. M. Leppink, 1995, The Annals of thoracic surgery.

Heterogeneity in Asthma Care in a Statewide Collaborative: the Ohio Pediatric Asthma Repository

Lisa J. Martin, Shalini G. Forbis, V. Pilipenko, 2015, Pediatrics.

Pulmonary function is compromised in children with mediastinal lymphoma.

K. McCoy, M. Ginn-Pease, D. King, 1997, Journal of pediatric surgery.

Small Interfering RNA Targeting T-cell Ig Mucin-3 Decreases Allergic Airway Inflammation and Hyperresponsiveness

K. McCoy, Wei-kun Hu, Jia-li Xu, 2013, Inflammation.

The clinical spectrum of chronic appendiceal abscess in cystic fibrosis.

K. McCoy, L. Taussig, E. Allen, 1992, American journal of diseases of children.

Chronic aspiration without gastroesophageal reflux as a cause of chronic respiratory symptoms in neurologically normal infants.

R. Castile, K. McCoy, R. Shell, 2001, Chest.

Galectin-9 ameliorates respiratory syncytial virus-induced pulmonary immunopathology through regulating the balance between Th17 and regulatory T cells.

K. McCoy, Yanli Wang, Peng Chen, 2015, Virus research.

Compression of the trachea by the innominate artery in a 2‐month‐old child

K. McCoy, R. Shell, E. Allen, 2001, Pediatric pulmonology.

Bronchopexy for congenital bronchomalacia in the newborn.

G. Besner, J. Menke, K. McCoy, 1999, Journal of pediatric surgery.

Lungs in infants and young children: improved thin-section CT with a noninvasive controlled-ventilation technique--initial experience.

R. Castile, K. McCoy, M. Hogan, 1999, Radiology.

Spirometric and endoscopic evaluation of airway collapse in infants with bronchopulmonary dysplasia

M. O'Keefe, K. McCoy, C. Bagwell, 1992, Pediatric pulmonology.

Airway microbiota across age and disease spectrum in cystic fibrosis

W. T. Harris, R. Gibson, J. Clancy, 2017, European Respiratory Journal.

Impact of elexacaftor–tezacaftor–ivacaftor on bacterial colonization and inflammatory responses in cystic fibrosis

B. Lewis, K. McCoy, N. Ryan-Wenger, 2022, Pediatric pulmonology.

Sleep-related breathing disorders.

K. McCoy, L. Taussig, C. Koopmann, 1981, American journal of otolaryngology.

Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation

J. Clancy, M. Ballmann, F. Accurso, 2011, Thorax.

Cystic fibrosis macrophage function and clinical outcomes after elexacaftor/tezacaftor/ivacaftor

K. McCoy, A. Amer, L. Hall-Stoodley, 2022, European Respiratory Journal.

Elexacaftor/Tezacaftor/Ivacaftor Improved Clinical Outcomes in an N1303K-CFTR Patient Based on in vitro Experimental Evidence.

K. McCoy, Yunjie Huang, A. Naren, 2021, American journal of respiratory and critical care medicine.

Clinical change 2 years from start of elexacaftor‐tezacaftor‐ivacaftor in severe cystic fibrosis

K. McCoy, S. Sheikh, Shasha Bai, 2023, Pediatric pulmonology.

Health literacy and willingness to use online health information by teens with asthma and diabetes.

A. McAlearney, W. Gardner, K. McCoy, 2011, Telemedicine journal and e-health : the official journal of the American Telemedicine Association.

Behavioral and nutritional treatment for preschool-aged children with cystic fibrosis: a randomized clinical trial.

R. Szczesniak, J. Clancy, S. Powers, 2015, JAMA pediatrics.

Behavioral and Nutritional Treatment for Preschool-Aged ChildrenWith Cystic Fibrosis

J. Clancy, J. Rausch, R. Castile, 2015 .

Stigma and optimism in adolescents and young adults with cystic fibrosis.

Cody Bok, C. Emery, K. McCoy, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Aerosolized recombinant human DNase in hospitalized cystic fibrosis patients with acute pulmonary exacerbations.

R. Amin, H. Fuchs, R. Moss, 1996, American journal of respiratory and critical care medicine.

Recurrent deep venous thrombosis complicating PICC line placement in two patients with cystic fibrosis and activated protein C-resistance

K. McCoy, B. Coley, M. Hogan, 1998, Pediatric Radiology.

Osteopathic Manipulative Treatment for Inpatients With Pulmonary Exacerbations of Cystic Fibrosis: Effects on Spirometry Findings and Patient Assessments of Breathing, Anxiety, and Pain

K. McCoy, David A. Swender, G. Thompson, 2014, The Journal of the American Osteopathic Association.

Impact of pulmonary hypertension on survival in patients with cystic fibrosis undergoing lung transplantation: an analysis of the UNOS registry.

B. Whitson, K. McCoy, R. Higgins, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Genome mosaicism is conserved but not unique in Pseudomonas aeruginosa isolates from the airways of young children with cystic fibrosis.

Samuel I. Miller, S. Lory, M. Olson, 2003, Environmental microbiology.

Compounded colistimethate as possible cause of fatal acute respiratory distress syndrome.

K. McCoy, 2007, The New England journal of medicine.

Outcomes of surgical management of severe GERD in patients with cystic fibrosis

K. McCoy, N. Ryan-Wenger, S. Sheikh, 2013, Pediatric pulmonology.

Children with Cystic Fibrosis Have Prolonged Chemical Clearance of Acid Reflux Compared to Symptomatic Children Without Cystic Fibrosis

F. Woodley, H. Mousa, K. McCoy, 2014, Digestive Diseases and Sciences.

Urinary metabolomics reveals unique metabolic signatures in infants with cystic fibrosis.

B. Ramsey, K. McCoy, E. Joseloff, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Splanchnic Uptake Of Leucine in Healthy Children and in Children with Cystic Fibrosis

K. McCoy, C. Horswill, C. L. Kien, 1999, Pediatric Research.

Effects of feeding on protein turnover in healthy children and in children with cystic fibrosis.

K. McCoy, C. Horswill, C. L. Kien, 1996, The American journal of clinical nutrition.

Effect of multiple courses of Aztreonam Lysine for Inhalation (AZLI) on FEV1 and weight in patients with cystic fibrosis (CF) and Pseudomonas aeruginosa (PA): Analysis of 18 month data from CP-AI-006

R. Gibson, K. McCoy, C. Oermann, 2009 .

Adherence over multiple courses of Aztreonam Lysine for Inhalation (AZLI): effect on disease-related endpoints in patients with cystic fibrosis (CF) and Pseudomonas aeruginosa (PA)

R. Gibson, A. Quittner, K. McCoy, 2009 .

Efficacy of Aztreonam Lysine for Inhalation (AZLI) in patients with cystic fibrosis and drug resistant P. aeruginosa (DRPA)

R. Gibson, K. McCoy, C. Oermann, 2009 .

Adult‐type pulmonary function tests in infants without respiratory disease

R. Castile, K. McCoy, D. Filbrun, 2000, Pediatric pulmonology.

Pragmatic evaluation of a midstream urine collection technique for infants in the emergency department.

N. Barrowman, K. McCoy, A. Plint, 2016, CJEM.

Improvement of hepatic steatosis in cystic fibrosis with ivacaftor therapy.

K. McCoy, D. Hayes, S. Sheikh, 2015, Journal of pediatric gastroenterology and nutrition.

Improving pediatric asthma care: A partnership between pediatric primary care clinics and a free-standing Children's Hospital

K. McCoy, N. Ryan-Wenger, S. Sheikh, 2016, The Journal of asthma : official journal of the Association for the Care of Asthma.

Inhaled mRNA therapy for treatment of cystic fibrosis: Interim results of a randomized, double-blind, placebo-controlled phase 1/2 clinical study.

T. Liou, K. McCoy, N. Lechtzin, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Effects of Tolbutamide on Growth and Body Composition of Nondiabetic Children with Cystic Fibrosis

K. McCoy, C. Horswill, W. Zipf, 1991, Pediatric Research.

Dexamethasone reduces IL-17 and Tim-3 expression in BALF of asthmatic mice

K. McCoy, Peng Chen, Wei-kun Hu, 2013, Journal of Huazhong University of Science and Technology [Medical Sciences].

Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis

K. McCoy, D. Hayes, S. Sheikh, 2017, World Journal of Pediatrics.

CT Imaging of Pediatric Patients with Cystic Fibrosis on Ivacaftor Therapy

K. McCoy, F. Long, D. Hayes, 2014, Lung.

Functional residual capacity (FRC) measurements by plethysmography and helium dilution in normal infants

E. Bar-Yishay, R. Castile, K. McCoy, 1995, Pediatric pulmonology.

Influence of diabetes on survival in patients with cystic fibrosis before and after lung transplantation.

B. Whitson, J. Tobias, K. McCoy, 2015, The Journal of thoracic and cardiovascular surgery.

Increased Fat Absorption From Enteral Formula Through an In-line Digestive Cartridge in Patients With Cystic Fibrosis

S. Freedman, K. McCoy, D. Orenstein, 2017, Journal of pediatric gastroenterology and nutrition.

Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study

A. Salvator, K. McCoy, D. Leung, 2019, Pediatric pulmonology.

Practitioner Due Diligence: Real-World Lumacaftor/Ivacaftor Use.

A. Salvator, K. McCoy, K. Novak, 2020, The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG.

Improvement in Bronchiectasis on CT Imaging in a Pediatric Patient with Cystic Fibrosis on Ivacaftor Therapy

K. McCoy, F. Long, S. Sheikh, 2014, Respiration.

Pulmonary Artery Pressure and Benefit of Lung Transplantation in Adult Cystic Fibrosis Patients.

J. Tobias, K. McCoy, D. Tumin, 2016, The Annals of thoracic surgery.

Cystic fibrosis macrophage function and clinical outcomes after elexacaftor/tezacaftor/ivacaftor

K. McCoy, A. Amer, L. Hall-Stoodley, 2022, European Respiratory Journal.

Burkholderia cenocepacia O polysaccharide chain contributes to caspase‐1‐dependent IL‐1β production in macrophages

C. Marsh, M. Valvano, K. McCoy, 2011, Journal of leukocyte biology.

Inhaled aztreonam lysine for chronic airway Pseudomonas aeruginosa in cystic fibrosis.

R. Gibson, A. Quittner, K. McCoy, 2008, American journal of respiratory and critical care medicine.

Impact of chronic medication de-escalation in patients with cystic fibrosis taking elexacaftor, tezacaftor, ivacaftor: A retrospective review.

K. McCoy, K. Novak, C. Nemastil, 2023, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Adjunctive Pharmacotherapies in Children With Asthma Exacerbations Requiring Continuous Albuterol Therapy: Findings From The Ohio Pediatric Asthma Repository.

Lisa J. Martin, N. Morris, G. K. Khurana Hershey, 2018, Hospital pediatrics.

Update on antibiotics for infection control in cystic fibrosis

K. McCoy, S. Kirkby, K. Novak, 2009, Expert review of anti-infective therapy.