Deanna M. Green

发表

Effect of Temperature on Cystic Fibrosis Lung Disease and Infections: A Replicated Cohort Study

Scott C. Bell, John McGready, Joseph M. Collaco, 2011, PloS one.

Location and duration of treatment of cystic fibrosis respiratory exacerbations do not affect outcomes.

G. Cutting, J. Collaco, P. Mogayzel, 2010, American journal of respiratory and critical care medicine.

Transient effectiveness of vitamin D2 therapy in pediatric cystic fibrosis patients.

S. Paranjape, P. Zeitlin, B. Rosenstein, 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Current treatment recommendations for correcting vitamin D deficiency in pediatric patients with cystic fibrosis are inadequate.

K. Carson, P. Zeitlin, B. Rosenstein, 2008, The Journal of pediatrics.

Environmental allergies and respiratory morbidities in cystic fibrosis

G. Cutting, G. Cutting, J. Collaco, 2013, Pediatric pulmonology.

Discontinuation versus continuation of hypertonic saline or dornase alfa in modulator treated people with cystic fibrosis (SIMPLIFY): results from two parallel, multicentre, open-label, randomised, controlled, non-inferiority trials.

Kapil M. Patel, D. Sanders, R. Gibson, 2022, The Lancet. Respiratory medicine.

Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients

G. Cutting, P. Sosnay, J. Collaco, 2010, Respiratory research.

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.

Sri V. V. Deevi, Kenneth G. C. Smith, K. Stirrups, 2018, The Journal of allergy and clinical immunology.

Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2

Fred A. Wright, Fei Zou, Clayton W. Commander, 2011, Nature Genetics.

Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis

Suzanne Cheng, M. Grow, M. Fallin, 2010, European Journal of Human Genetics.

Percutaneous Endoscopic Gastrostomy Tubes May Be Associated With Preservation of Lung Function in Patients With Cystic Fibrosis

E. Amankwah, Jacquelin Peck, N. Goldenberg, 2018, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.

Heritability of respiratory infection with Pseudomonas aeruginosa in cystic fibrosis.

G. Cutting, J. Collaco, S. Blackman, 2012, The Journal of pediatrics.

Cystic Fibrosis-Related Pancreatic Cysts Decrease in Size and Number Upon Treatment With Cystic Fibrosis Transmembrane Conductance Regulator Modulators.

M. Wilsey, Deanna M. Green, M. Kidder, 2020, Pancreas.

Cat and dog exposure and respiratory morbidities in cystic fibrosis.

G. Cutting, K. Raraigh, J. Collaco, 2014, The Journal of pediatrics.

The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of intervention

M. Sogin, H. Morrison, G. O’Toole, 2014, Microbiome.

Cystic fibrosis: a model for personalized genetic medicine.

Deanna M. Green, 2013, North Carolina medical journal.

The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of intervention

H. Morrison, G. Cutting, B. Stanton, 2014, Microbiome.

Location and duration of treatment of cystic fibrosis respiratory exacerbations do not affect outcomes.

G. Cutting, P. Mogayzel, K. Naughton, 2010, American journal of respiratory and critical care medicine.