B. Chatfield

发表

Role of endothelium-derived relaxing factor during transition of pulmonary circulation at birth.

S. Abman, I. McMurtry, I. McMurtry, 1990, The American journal of physiology.

Maturational changes in endothelium-derived relaxing factor activity of ovine pulmonary arteries in vitro.

D. Rodman, S. Abman, I. McMurtry, 1991, The American journal of physiology.

Effects of birth-related stimuli on L-arginine-dependent pulmonary vasodilation in ovine fetus.

D. Cornfield, S. Abman, I. McMurtry, 1992, The American journal of physiology.

A survey of the utilization of anti‐pseudomonal beta‐lactam therapy in cystic fibrosis patients

B. Marshall, Jared Cash, K. Ampofo, 2011, Pediatric pulmonology.

Associations of Sputum Biomarkers with Clinical Outcomes in People with Cystic Fibrosis

R. Szczesniak, J. Clancy, A. Quittner, 2022, medRxiv.

Growth hormone treatment improves growth and clinical status in prepubertal children with cystic fibrosis: results of a multicenter randomized controlled trial.

B. Adams-Huet, T. Ferkol, J. Rice, 2006, The Journal of clinical endocrinology and metabolism.

Diagnostic value of transbronchial, thoracoscopic, and open lung biopsy in immunocompetent children with chronic interstitial lung disease.

C. Kozinetz, L. Fan, H. Wojtczak, 1997, The Journal of pediatrics.

Vitamin D Deficiency in Pediatric Patients with Cystic Fibrosis: Associated Risk Factors in the Northern United States

J. Pohl, C. McDonald, A. Lansing, 2015, Southern medical journal.

Circulating immunoreactive endothelin-1 in children with pulmonary hypertension. Association with acute hypoxic pulmonary vasoreactivity.

R. Wolfe, S. Abman, M. Schaffer, 1993, The American review of respiratory disease.

Hemodynamic effects of endothelin-1 on ovine fetal pulmonary circulation.

S. Abman, I. McMurtry, I. McMurtry, 1991, The American journal of physiology.

EUR-1008 pancreatic enzyme replacement is safe and effective in patients with cystic fibrosis and pancreatic insufficiency.

K. Hardy, S. Boas, S. McColley, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pulmonary Nodules in a Newborn With ATP-Binding Cassette Transporter A3 (ABCA3) Mutations

S. Wert, L. Nogee, Derek A. Uchida, 2011, Pediatrics.

Long-term treatment with oral N-acetylcysteine: affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial.

C. Goss, J. Clancy, L. Herzenberg, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Rare loss of function variants in candidate genes and risk of colorectal cancer

Taylor J. Maxwell, Jennifer G. Robinson, Andrew J. Sanford, 2018, Human Genetics.

Cystic Fibrosis and Celiac Disease

J. Pohl, C. McDonald, A. Lowichik, 2010, Clinical pediatrics.

Clostridiumdifficile Infection and Proton Pump Inhibitor Use in Hospitalized Pediatric Cystic Fibrosis Patients

J. Pohl, E. Korgenski, M. Mackay, 2014 .

Clostridium difficile Infection and Proton Pump Inhibitor Use in Hospitalized Pediatric Cystic Fibrosis Patients

J. Pohl, E. Korgenski, M. Mackay, 2011, Gastroenterology research and practice.

Cystic Fibrosis and Celiac Disease: Both Can Occur Together.

J. Pohl, C. McDonald, A. Lowichik, 2010, Clinical pediatrics.

Prospective multicenter randomized patient recruitment and sample collection to enable future measurements of sputum biomarkers of inflammation in an observational study of cystic fibrosis

R. Keogh, J. Clancy, A. Quittner, 2019, BMC Medical Research Methodology.

Elevated immunoreactive endothelin-1 levels in newborn infants with persistent pulmonary hypertension.

S. Abman, A. Rosenberg, B. Chatfield, 1993, The Journal of pediatrics.

Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis.

Umer Khan, Margaret Rosenfeld, Peter Hiatt, 2011, Archives of pediatrics & adolescent medicine.

Duration of treatment effect after tobramycin solution for inhalation in young children with cystic fibrosis

J. Emerson, R. Gibson, F. Accurso, 2007, Pediatric pulmonology.

International phase III trial of liprotamase efficacy and safety in pancreatic-insufficient cystic fibrosis patients.

M. Campion, D. Borowitz, M. Cipolli, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pancreatic insufficiency, growth, and nutrition in infants identified by newborn screening as having cystic fibrosis.

F. Accurso, R. Sokol, K. Hambidge, 1992, The Journal of pediatrics.

High dose intermittent ticarcillin-clavulanate administration in pediatric cystic fibrosis patients.

Jared Cash, K. Ampofo, K. Korgenski, 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Population pharmacokinetic and pharmacodynamic modeling of high-dose intermittent ticarcillin-clavulanate administration in pediatric cystic fibrosis patients.

Jared Cash, C. Stockmann, K. Ampofo, 2011, Clinical therapeutics.

Short communication High dose intermittent ticarcillin-clavulanate administration in pediatric cystic fibrosis patients

Jared Cash, K. Ampofo, K. Korgenski, 2010 .