58 Publications (Page 2 of 3)
2015
Early Childhood Risk Factors for Decreased FEV1 at Age Six to Seven Years in Young Children with Cystic FibrosisSanders, Don B⋅Sanders, Don B⋅Sanders, Don B⋅Emerson, Julia⋅Emerson, Julia⋅Emerson, Julia⋅Ren, Clement L⋅Ren, Clement L⋅Ren, Clement L⋅Schechter, Michael S⋅Schechter, Michael S⋅Schechter, Michael S⋅Gibson, Ronald L⋅Gibson, Ronald L⋅Gibson, Ronald L⋅Morgan, Wayne⋅Morgan, Wayne⋅Morgan, Wayne⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret and Rosenfeld, MargaretAnnals of the American Thoracic Society, vol. 12, (no. 8), pp. 1176, 2015-Aug.
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Indeterminate cystic fibrosis newborn screening resultsRen, Clement L⋅Ren, Clement L⋅Parad, Richard⋅Parad, Richard⋅Borowitz, Drucy and Borowitz, DrucyPediatric Pulmonology, vol. 50, (no. 2), pp. 210, February 2015.
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Outcomes of Infants With Indeterminate Diagnosis Detected by Cystic Fibrosis Newborn ScreeningRen, Clement L⋅Ren, Clement L⋅Ren, Clement L⋅Fink, Aliza K⋅Fink, Aliza K⋅Fink, Aliza K⋅Petren, Kristofer⋅Petren, Kristofer⋅Petren, Kristofer⋅Borowitz, Drucy S⋅Borowitz, Drucy S⋅Borowitz, Drucy S⋅Mc Colley, Susanna A⋅McColley, Susanna A⋅McColley, Susanna A⋅Sanders, Don B⋅Sanders, Don B⋅Sanders, Don B⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Marshall, Bruce C⋅Marshall, Bruce C and Marshall, Bruce CPediatrics, vol. 135, (no. 6), pp. e1392, 2015-Jun.
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Prematurity and respiratory outcomes program (PROP): study protocol of a prospective multicenter study of respiratory outcomes of preterm infants in the United StatesPryhuber, Gloria S⋅Pryhuber, Gloria S⋅Maitre, Nathalie L⋅Maitre, Nathalie L⋅Ballard, Roberta A⋅Ballard, Roberta A⋅Cifelli, Denise⋅Cifelli, Denise⋅Davis, Stephanie D⋅Davis, Stephanie D⋅Ellenberg, Jonas H⋅Ellenberg, Jonas H⋅Greenberg, James M⋅Greenberg, James M⋅Kemp, James⋅Kemp, James⋅Mariani, Thomas J⋅Mariani, Thomas J⋅Panitch, Howard⋅Panitch, Howard⋅Ren, Clement⋅Ren, Clement⋅Shaw, Pamela⋅Shaw, Pamela⋅Taussig, Lynn M⋅Taussig, Lynn M⋅Hamvas, Aaron and Hamvas, AaronBMC pediatrics, vol. 15, (no. 1), pp. 37, 2015-Apr-10.
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Risk factors for lung function decline in a large cohort of young cystic fibrosis patientsCogen, Jonathan⋅Cogen, Jonathan⋅Cogen, Jonathan⋅Emerson, Julia⋅Emerson, Julia⋅Emerson, Julia⋅Sanders, Don B⋅Sanders, Don B⋅Sanders, Don B⋅Ren, Clement⋅Ren, Clement⋅Ren, Clement⋅Schechter, Michael S⋅Schechter, Michael S⋅Schechter, Michael S⋅Gibson, Ronald L⋅Gibson, Ronald L⋅Gibson, Ronald L⋅Morgan, Wayne⋅Morgan, Wayne⋅Morgan, Wayne⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret and Rosenfeld, MargaretPediatric Pulmonology, vol. 50, (no. 8), pp. 770, August 2015.
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2014
ATS core curriculum 2014: part IV. Pediatric pulmonary medicineNevin, Mary A⋅Nevin, Mary A⋅Daines, Cori L⋅Daines, Cori L⋅Redding, Gregory J⋅Redding, Gregory J⋅Ren, Clement L⋅Ren, Clement L⋅Ratjen, Felix A⋅Ratjen, Felix A⋅Shah, Avani V⋅Shah, Avani V⋅Hiranrattana, Anunya⋅Hiranrattana, Anunya⋅Alexiou, Stamatia⋅Alexiou, Stamatia⋅Bansal, Manvi⋅Bansal, Manvi⋅Pizarro-Gamboa, Maria E⋅Pizarro-Gamboa, Maria E⋅Panitch, Howard B and Panitch, Howard BAnnals of the American Thoracic Society, vol. 11, (no. 10), pp. 1639, 2014-Dec.
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Chloral hydrate sedation for infant pulmonary function testingRen, Clement L⋅Ren, Clement L⋅Ren, C.L.⋅Robinson, Paul⋅Robinson, P.⋅Robinson, Paul⋅Ranganathan, Sarath⋅Ranganathan, Sarath and Ranganathan, S.Pediatric Pulmonology, vol. 49, (no. 12), pp. 1252, December 2014.
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Early childhood wheezing is associated with lower lung function in cystic fibrosisRen, Clement L⋅Ren, Clement L⋅Konstan, Michael W⋅Konstan, Michael W⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Pasta, David J⋅Pasta, David J⋅Millar, Stefanie J⋅Millar, Stefanie J⋅Morgan, Wayne J and Morgan, Wayne JPediatric Pulmonology, vol. 49, (no. 8), pp. 750, August 2014.
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2013
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 AgeRosenfeld, M.⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Allen, Julian⋅Allen, J.⋅Allen, Julian⋅Arets, Bert H⋅Arets, Bert H G M⋅Arets, B.H.G.M.⋅Aurora, Paul⋅Aurora, Paul⋅Aurora, P.⋅Beydon, Nicole⋅Beydon, N.⋅Beydon, Nicole⋅Calogero, Claudia⋅Calogero, C.⋅Calogero, Claudia⋅Castile, Robert G⋅Castile, R.G.⋅Castile, Robert G⋅Davis, S.D.⋅Davis, Stephanie D⋅Davis, Stephanie D⋅Fuchs, Susanne⋅Fuchs, S.⋅Fuchs, Susanne⋅Gappa, Monika⋅Gappa, M.⋅Gappa, Monika⋅Gustaffson, Per M⋅Gustaffson, P.M.⋅Gustaffson, Per M⋅Hall, Graham L⋅Hall, G.L.⋅Hall, Graham L⋅Jones, Marcus Herbert⋅Jones, Marcus H⋅Jones, M.H.⋅Kirkby, Jane C⋅Kirkby, J.C.⋅Kirkby, Jane C⋅Kraemer, Richard⋅Kraemer, Richard⋅Kraemer, R.⋅Lombardi, Enrico⋅Lombardi, E.⋅Lombardi, Enrico⋅Lum, S.⋅Lum, Sooky⋅Lum, Sooky⋅Mayer, Oscar H⋅Mayer, Oscar H⋅Mayer, O.H.⋅Merkus, Peter⋅Merkus, Peter⋅Merkus, P.⋅Nielsen, Kim G⋅Nielsen, Kim G⋅Nielsen, K.G.⋅Oliver, C.⋅Oliver, Cara⋅Oliver, Cara⋅Oostveen, Ellie⋅Oostveen, Ellie⋅Oostveen, E.⋅Ranganathan, Sarath⋅Ranganathan, Sarath⋅Ranganathan, S.⋅Ren, Clement L⋅Ren, Clement L⋅Ren, C.L.⋅Robinson, Paul D⋅Robinson, Paul D⋅Robinson, P.D.⋅Seddon, Paul C⋅Seddon, P.C.⋅Seddon, Paul C⋅Sly, Peter D⋅Sly, Peter D⋅Sly, P.D.⋅Sockrider, M.M.⋅Sockrider, Marianna M⋅Sockrider, Marianna M⋅Sonnappa, Samatha⋅Sonnappa, Samatha⋅Sonnappa, S.⋅Stocks, Janet⋅Stocks, J.⋅Stocks, Janet⋅Subbarao, Padmaja⋅Subbarao, Padmaja⋅Subbarao, P.⋅Tepper, Robert S⋅Tepper, R.S.⋅Tepper, Robert S⋅Vilozni, Daphna⋅Vilozni, Daphna and Vilozni, D.Annals of the American Thoracic Society, vol. 10, (no. 2), pp. S11, 2013-Apr.
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Treatment complexity in cystic fibrosis: Trends over time and associations with site-specific outcomesSawicki, Gregory⋅Sawicki, Gregory S⋅Ren, Clement⋅Ren, Clement L⋅Konstan, Michael W⋅Konstan, Michael⋅Millar, Stefanie⋅Millar, Stefanie J⋅Pasta, David J⋅Pasta, David⋅Quittner, Alexandra and Quittner, Alexandra LJournal of Cystic Fibrosis, vol. 12, (no. 5), pp. 467, 2013.
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2012
Analysis of the associations between lung function and clinical features in preschool children with Cystic FibrosisRen, Clement L⋅Ren, Clement L⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Mayer, Oscar H⋅Mayer, Oscar H⋅Davis, Stephanie D⋅Davis, Stephanie D⋅Kloster, Margaret⋅Kloster, Margaret⋅Castile, Robert G⋅Castile, Robert G⋅Hiatt, Peter W⋅Hiatt, Peter W⋅Hart, Meeghan⋅Hart, Meeghan⋅Johnson, Robin⋅Johnson, Robin⋅Jones, Paul⋅Jones, Paul⋅Brumback, Lyndia C⋅Brumback, Lyndia C⋅Kerby, Gwendolyn S and Kerby, Gwendolyn SPediatric Pulmonology, vol. 47, (no. 6), pp. 581, June 2012.
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Lung function distinguishes preschool children with CF from healthy controls in a multi‐center settingKerby, Gwendolyn S⋅Kerby, Gwendolyn S⋅Kerby, Gwendolyn S⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Rosenfeld, Margaret⋅Ren, Clement L⋅Ren, Clement L⋅Ren, Clement L⋅Mayer, Oscar H⋅Mayer, Oscar H⋅Mayer, Oscar H⋅Brumback, Lyndia⋅Brumback, Lyndia⋅Brumback, Lyndia⋅Castile, Robert⋅Castile, Robert⋅Castile, Robert⋅Hart, Meeghan A⋅Hart, Meeghan A⋅Hart, Meeghan A⋅Hiatt, Peter⋅Hiatt, Peter⋅Hiatt, Peter⋅Kloster, Margaret⋅Kloster, Margaret⋅Kloster, Margaret⋅Johnson, Robin⋅Johnson, Robin⋅Johnson, Robin⋅Jones, Paul⋅Jones, Paul⋅Jones, Paul⋅Davis, Stephanie D⋅Davis, Stephanie D and Davis, Stephanie DPediatric Pulmonology, vol. 47, (no. 6), pp. 605, June 2012.
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Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosisRen, Clement L⋅Ren, Clement⋅Konstan, Michael W⋅Konstan, Michael⋅Yegin, Ashley⋅Yegin, Ashley⋅Rasouliyan, Lawrence⋅Rasouliyan, Lawrence⋅Trzaskoma, Benjamin⋅Trzaskoma, Benjamin⋅Morgan, Wayne⋅Morgan, Wayne⋅Regelmann, Warren E and Regelmann, WarrenJournal of Cystic Fibrosis, vol. 11, (no. 4), pp. 299, 2012.
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Risk factors for onset of persistent respiratory symptoms in children with cystic fibrosisMc Colley, Susanna⋅McColley, Susanna A⋅Ren, Clement L⋅Ren, Clement L⋅Schechter, Michael S⋅Schechter, Michael S⋅Regelmann, Warren E⋅Regelmann, Warren E⋅Pasta, David J⋅Pasta, David J⋅Konstan, Michael W and Konstan, Michael WPediatric Pulmonology, vol. 47, (no. 10), pp. 972, October 2012.
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2011
Clinical outcomes in infants with cystic fibrosis transmembrane conductance regulator (CFTR) related metabolic syndromeRen, Clement L⋅Ren, Clement L⋅Desai, Harsh⋅Desai, Harsh⋅Platt, Mary⋅Platt, Mary⋅Dixon, Marissa and Dixon, MarissaPediatric Pulmonology, vol. 46, (no. 11), pp. 1084, November 2011.
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2010
Baseline Characteristics and Factors Associated With Nutritional and Pulmonary Status at Enrollment in the Cystic Fibrosis EPIC Observational CohortRosenfeld, Margaret⋅Rosenfeld, Margaret⋅Emerson, Julia⋅Emerson, Julia C⋅McNamara, Sharon⋅McNamara, Sharon⋅Joubran, Kelli⋅Joubran, Kelli⋅Retsch-Bogart, George⋅Retsch‐Bogart, George⋅Graff, Gavin R⋅Graff, Gavin R⋅Gutierrez, Hector H⋅Gutierrez, Hector H⋅Kanga, Jamshed F⋅Kanga, Jamshed F⋅Lahiri, Thomas⋅Lahiri, Thomas⋅Noyes, Blake⋅Noyes, Blake⋅Ramsey, Bonnie⋅Ramsey, Bonnie⋅Ren, Clement L⋅Ren, Clement L⋅Schechter, Michael⋅Schechter, Michael⋅Morgan, Wayne⋅Morgan, Wayne⋅Gibson, Ronald L and Gibson, Ronald LPediatric Pulmonology, vol. 45, (no. 9), pp. 944, September 2010.
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2009
The Impact of MRSA on Lung Function in Patients with Cystic FibrosisSawicki, Gregory S⋅Dasenbrook, Elliott C.⋅Sawicki, Gregory S⋅Merlo, Christian A.⋅Rasouliyan, Lawrence⋅Rasouliyan, Lawrence⋅Lechtzin, Noah⋅Ren, Clement L⋅Ren, Clement L and Boyle, Michael P.American journal of respiratory and critical care medicine, vol. 179, (no. 8), pp. 735, 2009-Apr-15.
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The Impact of MRSA on Lung Function in Patients with Cystic Fibrosis/From the AuthorsSawicki, Gregory S⋅Sawicki, Gregory⋅Rasouliyan, Lawrence⋅Rasouliyan, Lawrence⋅Ren, Clement L⋅Ren, Clement⋅Dasenbrook, Elliott⋅Dasenbrook, Elliott C⋅Merlo, Christian⋅Merlo, Christian A⋅Lechtzin, Noah⋅Lechtzin, Noah⋅Boyle, Michael and Boyle, Michael PAmerican Journal of Respiratory and Critical Care Medicine, vol. 179, (no. 8), pp. 734, 20090415.
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2008
Assessment and monitoring of cystic fibrosis lung disease in infants and young childrenRen, Clement L and Ren, Clement LExpert Review of Respiratory Medicine, vol. 2, (no. 3), pp. 390, 6/1/2008.
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Cystic Fibrosis: Evolution from a Fatal Disease of Infancy with a Clear Phenotype to a Chronic Disease of Adulthood with Diverse ManifestationsRen, Clement L and Ren, ClementClinical Reviews in Allergy & Immunology, vol. 35, (no. 3), pp. 99, 20081200.
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The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosisSawicki, Gregory S⋅Sawicki, Gregory S⋅Rasouliyan, Lawrence⋅Rasouliyan, Lawrence⋅Pasta, David J⋅Pasta, David J⋅Regelmann, Warren E⋅Regelmann, Warren E⋅Wagener, Jeffrey S⋅Wagener, Jeffrey S⋅Waltz, David A⋅Waltz, David A⋅Ren, Clement L and Ren, Clement LPediatric Pulmonology, vol. 43, (no. 11), pp. 1123, November 2008.
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Trends in the clinical characteristics of the U.S. cystic fibrosis patient population from 1995 to 2005VanDevanter, Donald R⋅VanDevanter, Donald R⋅Rasouliyan, Lawrence⋅Rasouliyan, Lawrence⋅Murphy, Thomas M⋅Murphy, Thomas M⋅Morgan, Wayne⋅Morgan, Wayne J⋅Ren, Clement L⋅Ren, Clement L⋅Konstan, Michael W⋅Konstan, Michael W⋅Wagener, Jeffrey S and Wagener, Jeffrey SPediatric Pulmonology, vol. 43, (no. 8), pp. 744, August 2008.
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2007
Infant Care Patterns at Epidemiologic Study of Cystic Fibrosis Sites That Achieve Superior Childhood Lung FunctionPadman, Raj⋅Padman, Raj⋅McColley, Susanna⋅Mc Colley, Susanna⋅Miller, Dave P⋅Miller, Dave⋅Konstan, Michael⋅Konstan, Michael W⋅Morgan, Wayne⋅Morgan, Wayne⋅Schechter, Michael⋅Schechter, Michael S⋅Ren, Clement⋅Ren, Clement L⋅Wagener, Jeffrey⋅Wagener, Jeffrey S and InvestigatorsPediatrics, vol. 119, (no. 3), pp. e537, 20070301.
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Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function.(ABSTRACT)(Clinical report)Padman, Raj⋅McColley, Susanna⋅Miller, Dave⋅Konstan, Michael⋅Morgan, Wayne⋅Schechter, Michael⋅Ren, Clement and Wagener, JeffreyPediatrics, vol. 119, (no. 3), pp. 588, 20070301.
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