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Clinical Findings in Adolescents Hospitalized With EVALI; Novel Report on Coagulopathy; Hospital Pediatrics; (2022).

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Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial; Lancet Respiratory Medicine; (2017).

Household proximity to water and nontuberculous mycobacteria in children with cystic fibrosis; Pediatric Pulmonology; (2017).

Forced Expiratory Volume in 1 Second Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function; Journal of Pediatrics; (2016).

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Hypoxic and hypercapnic ventilatory responses in Prader-Willi syndrome; Journal of Applied Physiology; (1994).

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