| Year |
Citation |
Score |
| 2024 |
Kua KL, Rhoads E, Slaven JE, Edwards S, Haas DM, Ren CL, Tiller C, Bjerregaard J, Haneline LS, Tepper RS. Decreased vascular reactivity associated with increased IL-8 in 6-month-old infants of mothers with pre-eclampsia. Pediatric Research. PMID 38509229 DOI: 10.1038/s41390-024-03132-4 |
0.457 |
|
| 2022 |
Ren CL, Slaven JE, Haas DM, Haneline LS, Rrt CT, Hogg G, Rrt JB, Tepper RS. Forced Expiratory Flows and Diffusion Capacity in Infants Born from Mothers with Pre-eclampsia. Pediatric Pulmonology. PMID 35796049 DOI: 10.1002/ppul.26064 |
0.452 |
|
| 2022 |
Voynow JA, Feng R, Ren CL, Dylag AM, Kemp JS, McDowell K, Sharp J, Moore PE, Eichenwald E, Panitch H, Clem C, Johnson R, Davis SD. Pulmonary function tests in extremely low gestational age infants at one year of age. Pediatric Pulmonology. 57: 435-447. PMID 34779149 DOI: 10.1002/ppul.25757 |
0.515 |
|
| 2021 |
Madde A, Okoniewski W, Sanders DB, Ren CL, Weiner DJ, Forno E. Nutritional status and lung function in children with pancreatic-sufficient cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 34972650 DOI: 10.1016/j.jcf.2021.12.014 |
0.518 |
|
| 2021 |
Cristea AI, Ren CL, Amin R, Eldredge LC, Levin JC, Majmudar PP, May AE, Rose RS, Tracy MC, Watters KF, Allen J, Austin ED, Cataletto ME, Collaco JM, Fleck RJ, et al. Outpatient Respiratory Management of Infants, Children, and Adolescents with Post-Prematurity Respiratory Disease: An Official American Thoracic Society Clinical Practice Guideline. American Journal of Respiratory and Critical Care Medicine. 204: e115-e133. PMID 34908518 DOI: 10.1164/rccm.202110-2269ST |
0.303 |
|
| 2021 |
Muston HN, Slaven JE, Tiller C, Clem C, Ferkol TW, Ranganathan S, Davis SD, Ren CL. Hyperinflation is associated with increased respiratory rate and is a more sensitive measure of cystic fibrosis lung disease during infancy compared to forced expiratory measures. Pediatric Pulmonology. PMID 34143539 DOI: 10.1002/ppul.25538 |
0.557 |
|
| 2020 |
Barben J, Castellani C, Munck A, Davies JC, deWinter K, Gartner S, Kashirskaya N, Linnane B, Mayell SJ, McColley S, Ooi CY, Proesmans M, Ren CL, Salinas D, Sands D, et al. Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID). Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 33257262 DOI: 10.1016/j.jcf.2020.11.006 |
0.303 |
|
| 2020 |
McColley SA, Elbert A, Wu R, Ren CL, Sontag MK, LeGrys VA. Quantity not sufficient rates and delays in sweat testing in US infants with cystic fibrosis. Pediatric Pulmonology. PMID 32797669 DOI: 10.1002/Ppul.25027 |
0.3 |
|
| 2020 |
Dylag AM, Kopin HG, O'Reilly MA, Wang H, Davis SD, Ren CL, Pryhuber GS. Early Neonatal Oxygen Exposure Predicts Pulmonary Morbidity and Functional Deficits at 1 Year. The Journal of Pediatrics. 223: 20-28.e2. PMID 32711747 DOI: 10.1016/J.Jpeds.2020.04.042 |
0.486 |
|
| 2020 |
Voynow JA, Fisher K, Sunday ME, Cotten CM, Hamvas A, Hendricks-Muñoz KD, Poindexter BB, Pryhuber GS, Ren CL, Ryan RM, Sharp JK, Young SP, Zhang H, Greenberg RG, Herring AH, et al. Urine gastrin-releasing peptide in the first week correlates with bronchopulmonary dysplasia and post-prematurity respiratory disease. Pediatric Pulmonology. PMID 31995668 DOI: 10.1002/Ppul.24665 |
0.448 |
|
| 2018 |
Ren CL, Feng R, Davis SD, Eichenwald E, Jobe A, Moore PE, Panitch HB, Sharp JK, Kisling J, Clem C, Kemp JS. Tidal Breathing Measurements at Discharge and Clinical Outcomes in Extremely Low Gestational Age Neonates. Annals of the American Thoracic Society. PMID 30088802 DOI: 10.1513/Annalsats.201802-112Oc |
0.469 |
|
| 2017 |
Auten R, Ren C, Yilmaz O, Noah TL. Pediatric pulmonology year in review 2016: Part 2. Pediatric Pulmonology. PMID 28440920 DOI: 10.1002/Ppul.23719 |
0.332 |
|
| 2016 |
Ren CL, Esther CR, Debley JS, Sockrider M, Yilmaz O, Amin N, Bazzy-Asaad A, Davis SD, Durand M, Ewig JM, Yuksel H, Lombardi E, Noah TL, Radford P, Ranganathan S, et al. Official American Thoracic Society Clinical Practice Guidelines: Diagnostic Evaluation of Infants with Recurrent or Persistent Wheezing. American Journal of Respiratory and Critical Care Medicine. 194: 356-73. PMID 27479061 DOI: 10.1164/Rccm.201604-0694St |
0.448 |
|
| 2016 |
Auten R, Schwarze J, Ren C, Davis S, Noah TL. Pediatric Pulmonology year in review 2015: Part 1. Pediatric Pulmonology. PMID 27124279 DOI: 10.1002/Ppul.23423 |
0.515 |
|
| 2015 |
Cogen J, Emerson J, Sanders DB, Ren C, Schechter MS, Gibson RL, Morgan W, Rosenfeld M. Risk factors for lung function decline in a large cohort of young cystic fibrosis patients. Pediatric Pulmonology. 50: 763-70. PMID 26061914 DOI: 10.1002/Ppul.23217 |
0.327 |
|
| 2015 |
Ren CL, Fink AK, Petren K, Borowitz DS, McColley SA, Sanders DB, Rosenfeld M, Marshall BC. Outcomes of infants with indeterminate diagnosis detected by cystic fibrosis newborn screening. Pediatrics. 135: e1386-92. PMID 25963008 DOI: 10.1542/Peds.2014-3698 |
0.301 |
|
| 2015 |
Pryhuber GS, Maitre NL, Ballard RA, Cifelli D, Davis SD, Ellenberg JH, Greenberg JM, Kemp J, Mariani TJ, Panitch H, Ren C, Shaw P, Taussig LM, Hamvas A. Prematurity and respiratory outcomes program (PROP): study protocol of a prospective multicenter study of respiratory outcomes of preterm infants in the United States. Bmc Pediatrics. 15: 37. PMID 25886363 DOI: 10.1186/S12887-015-0346-3 |
0.532 |
|
| 2015 |
Ren CL, Parad R, Borowitz D. Indeterminate cystic fibrosis newborn screening results. Pediatric Pulmonology. 50: 209-10. PMID 24760681 DOI: 10.1002/Ppul.23055 |
0.522 |
|
| 2013 |
Rosenfeld M, Allen J, Arets BH, Aurora P, Beydon N, Calogero C, Castile RG, Davis SD, Fuchs S, Gappa M, Gustaffson PM, Hall GL, Jones MH, Kirkby JC, Kraemer R, ... ... Ren CL, et al. 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. Annals of the American Thoracic Society. 10: S1-S11. PMID 23607855 DOI: 10.1513/Annalsats.201301-017St |
0.626 |
|
| 2012 |
Ren CL, Rosenfeld M, Mayer OH, Davis SD, Kloster M, Castile RG, Hiatt PW, Hart M, Johnson R, Jones P, Brumback LC, Kerby GS. Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosis. Pediatric Pulmonology. 47: 574-81. PMID 22081584 DOI: 10.1002/Ppul.21590 |
0.499 |
|
| 2012 |
Kerby GS, Rosenfeld M, Ren CL, Mayer OH, Brumback L, Castile R, Hart MA, Hiatt P, Kloster M, Johnson R, Jones P, Davis SD. Lung function distinguishes preschool children with CF from healthy controls in a multi-center setting. Pediatric Pulmonology. 47: 597-605. PMID 22081559 DOI: 10.1002/Ppul.21589 |
0.502 |
|
| 2010 |
Rosenfeld M, Emerson J, McNamara S, Joubran K, Retsch-Bogart G, Graff GR, Gutierrez HH, Kanga JF, Lahiri T, Noyes B, Ramsey B, Ren CL, Schechter M, Morgan W, Gibson RL, et al. Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort. Pediatric Pulmonology. 45: 934-44. PMID 20597081 DOI: 10.1002/Ppul.21279 |
0.305 |
|
| 2008 |
Ren CL. Assessment and monitoring of cystic fibrosis lung disease in infants and young children. Expert Review of Respiratory Medicine. 2: 381-90. PMID 20477200 DOI: 10.1586/17476348.2.3.381 |
0.347 |
|
| 2007 |
Padman R, McColley SA, Miller DP, Konstan MW, Morgan WJ, Schechter MS, Ren CL, Wagener JS. Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function. Pediatrics. 119: e531-7. PMID 17332172 DOI: 10.1542/peds.2006-1414 |
0.334 |
|
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