Search Results - "Castile, Robert"

Respiratory Morbidity and Lung Function in Preterm Infants of 32 to 36 Weeks' Gestational Age by COLIN, Andrew A, MCEVOY, Cynthia, CASTILE, Robert G

“…Normal lung development follows a series of orchestrated events. Premature birth interrupts normal in utero lung development, which results in significant…”
Get full text

An Official American Thoracic Society Clinical Practice Guideline: Classification, Evaluation, and Management of Childhood Interstitial Lung Disease in Infancy by KURLAND, Geoffrey, DETERDING, Robin R, LANGSTON, Claire, NOGEE, Lawrence M, REDDING, Gregory J, HAGOOD, James S, YOUNG, Lisa R, BRODY, Alan S, CASTILE, Robert G, DELL, Sharon, FAN, Leland L, HAMVAS, Aaron, HILMAN, Bettina C

“…There is growing recognition and understanding of the entities that cause interstitial lung disease (ILD) in infants. These entities are distinct from those…”
Get full text

Mechanisms of cough provocation and cough resolution in neonates with bronchopulmonary dysplasia by Jadcherla, Sudarshan R., Hasenstab, Kathryn A., Shaker, Reza, Castile, Robert G.

“…Background: Cough and deglutition are protective mechanisms that defend against aspiration. We identified mechanisms associated with cough provocation as well…”
Get full text

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 by Rosenfeld, Margaret, Allen, Julian, Arets, Bert H G M, Aurora, Paul, Beydon, Nicole, Calogero, Claudia, Castile, Robert G, Davis, Stephanie D, Fuchs, Susanne, Gappa, Monika, Gustaffson, Per M, Hall, Graham L, Jones, Marcus H, Kirkby, Jane C, Kraemer, Richard, Lombardi, Enrico, Lum, Sooky, Mayer, Oscar H, Merkus, Peter, Nielsen, Kim G, Oliver, Cara, Oostveen, Ellie, Ranganathan, Sarath, Ren, Clement L, Robinson, Paul D, Seddon, Paul C, Sly, Peter D, Sockrider, Marianna M, Sonnappa, Samatha, Stocks, Janet, Subbarao, Padmaja, Tepper, Robert S, Vilozni, Daphna

“…Although pulmonary function testing plays a key role in the diagnosis and management of chronic pulmonary conditions in children under 6 years of age,…”
Get full text

Multicenter Evaluation of Infant Lung Function Tests as Cystic Fibrosis Clinical Trial Endpoints by DAVIS, Stephanie D, ROSENFELD, Margaret, MOGAYZEL, Peter J, JOHNSON, Robin C, WILCOX, Stephanie L, CASTILE, Robert G, KERBY, Gwendolyn S, BRUMBACK, Lyndia, KLOSTER, Margaret H, ACTON, James D, COLIN, Andrew A, CONRAD, Carol K, HART, Meeghan A, HIATT, Peter W

“…The conducting of clinical trials in infants with cystic fibrosis (CF) has been hindered by lack of sensitive outcome measures. To evaluate safety,…”
Get full text

723 Distinguishing the Effects of the Proximal Migration of Gastro-Esophageal Reflux (GER) on Symptoms and Characteristics of Refluxate in Premature Infants by Jadcherla, Sudarshan, Wagner, Alecia, Gao, Xiaoyu, Castile, Robert G, Shaker, Reza

Get full text

Tu1974 Do Nasal Respiratory Support Breathing Methods Influence Pharyngeal Provocation Induced Reflex Responses in Infants With Chronic Lung Disease (CLD)? by Jadcherla, Sudarshan, Hasenstab, Kathryn, Gao, Xiaoyu, Castile, Robert G, Shaker, Reza

Get full text

Gestational and postnatal modulation of esophageal sphincter reflexes in human premature neonates by Jadcherla, Sudarshan R., Shubert, Theresa R., Malkar, Manish B., Sitaram, Swetha, Moore, Rebecca K., Wei, Lai, Fernandez, Soledad, Castile, Robert G.

“…Background: Effects of gestational age (GA) and postnatal maturation on upper and lower esophageal sphincter (UES and LES) reflex development remain unclear…”
Get full text

Structural airway abnormalities in infants and young children with cystic fibrosis by Long, Frederick R, Williams, Roger S, Castile, Robert G

“…To determine whether the airway structure of infants and young children with cystic fibrosis (CF) differs from that of normal children by using high-resolution…”
Get full text

Association of lung function, chest radiographs and clinical features in infants with cystic fibrosis by ROSENFELD, Margaret, FARRELL, Philip M, HART, Meeghan A, KERBY, Gwendolyn S, HIATT, Peter W, MOGAYZEL, Peter J, JOHNSON, Robin C, DAVIS, Stephanie D, KLOSTER, Margaret, SWANSON, Jonathan O, VU, Thuy, BRUMBACK, Lyndia, ACTON, James D, CASTILE, Robert G, COLIN, Andrew A, CONRAD, Carol K

“…The optimal strategy for monitoring cystic fibrosis lung disease in infancy remains unclear. Our objective was to describe longitudinal associations between…”
Get full text

Behavioral and nutritional treatment for preschool-aged children with cystic fibrosis: a randomized clinical trial by Powers, Scott W, Stark, Lori J, Chamberlin, Leigh A, Filigno, Stephanie S, Sullivan, Stephanie M, Lemanek, Kathleen L, Butcher, Jennifer L, Driscoll, Kimberly A, Daines, Cori L, Brody, Alan S, Schindler, Teresa, Konstan, Michael W, McCoy, Karen S, Nasr, Samya Z, Castile, Robert G, Acton, James D, Wooldridge, Jamie L, Ksenich, Roberta A, Szczesniak, Rhonda D, Rausch, Joseph R, Stallings, Virginia A, Zemel, Babette S, Clancy, John P

“…Evidence-based treatments that achieve optimal energy intake and improve growth in preschool-aged children with cystic fibrosis (CF) are a critical need. To…”
Get more information

Su1104 Esophageal Dysmotility During Cardio-Respiratory Events in Infants With Apparent Life Threatening Events by Hasenstab, Kathryn, Chan, Chin Yee, Castile, Robert G, Shaker, Reza, Jadcherla, Sudarshan R

Get full text

Tu1199 Hyperactive Upper Esophageal Sphincter and Esophageal Reflexes in Chronic Lung Disease of Infants: Potential Mechanism for Pulmonary Symptoms by Jadcherla, Sudarshan R, Hasenstab, Kathryn, Chan, Chin Yee, Moore, Rebecca K, Castile, Robert G, Shaker, Reza

Get full text

Analysis of the associations between lung function and clinical features in preschool children with Cystic Fibrosis by Ren, Clement L., Rosenfeld, Margaret, Mayer, Oscar H., Davis, Stephanie D., Kloster, Margaret, Castile, Robert G., Hiatt, Peter W., Hart, Meeghan, Johnson, Robin, Jones, Paul, Brumback, Lyndia C., Kerby, Gwendolyn S.

“…Objective To analyze cross‐sectional and longitudinal associations between lung function measures and clinical features in a cohort of preschool children with…”
Get full text

Pulmonary function in bronchopulmonary dysplasia by Robin, Beverley, Kim, Young-Jee, Huth, Jaimee, Klocksieben, Jim, Torres, Margaret, Tepper, Robert S., Castile, Robert G., Solway, Julian, Hershenson, Marc B., Goldstein-Filbrun, Amy

“…The purpose of this study was to examine lung function and bronchodilator responsiveness in infants with a history of prematurity and bronchopulmonary…”
Get full text

Lessons learned from a randomized trial of airway secretion clearance techniques in cystic fibrosis by Sontag, Marci K., Quittner, Alexandra L., Modi, Avani C., Koenig, Joni M., Giles, Don, Oermann, Christopher M., Konstan, Michael W., Castile, Robert, Accurso, Frank J.

“…Rationale Airway secretion clearance therapies are a cornerstone of cystic fibrosis care, however longitudinal comparative studies are rare. Our objectives…”
Get full text

Sa1453 Mechanisms of Origin and Resolution of Cough Reflex in Human Neonates by Jadcherla, Sudarshan R, Hasenstab, Kathryn, Hoyng, Jillian M, Moore, Rebecca K, Castile, Robert G, Shaker, Reza

Get full text

Volume-monitored chest CT: a simplified method for obtaining motion-free images near full inspiratory and end expiratory lung volumes by Mueller, Kathryn S., Long, Frederick R., Flucke, Robert L., Castile, Robert G.

“…Background Lung inflation and respiratory motion during chest CT affect diagnostic accuracy and reproducibility. Objective To describe a simple…”
Get full text

Computed Tomography in the Evaluation of Cystic Fibrosis Lung Disease by Brody, Alan S, Tiddens, Harm A. W. M, Castile, Robert G, Coxson, Harvey O, de Jong, Pim A, Goldin, Jonathan, Huda, Walter, Long, Frederick R, McNitt-Gray, Michael, Rock, Michael, Robinson, Terry E, Sagel, Scott D, CT Scanning in Cystic Fibrosis Special Interest Group

“…The first report of computed tomography (CT) scanning to monitor cystic fibrosis (CF)-related lung disease was published in 1986. Further publications…”
Get full text

Image Analysis for Cystic Fibrosis: Computer-Assisted Airway Wall and Vessel Measurements from Low-Dose, Limited Scan Lung CT Images by Mumcuoğlu, Erkan Ü., Long, Frederick R., Castile, Robert G., Gurcan, Metin N.

“…Cystic fibrosis (CF) is a life-limiting genetic disease that affects approximately 30,000 Americans. When compared to those of normal children, airways of…”
Get full text