Clement L Ren

Summary

Affiliation: University of Rochester
Country: USA

Publications

  1. pmc Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis
    Clement L Ren
    University of Rochester, Rochester, NY, USA
    J Cyst Fibros 11:293-9. 2012
  2. doi request reprint Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosis
    Clement L Ren
    University of Rochester, Rochester, New York 14642, USA
    Pediatr Pulmonol 47:574-81. 2012
  3. doi request reprint Clinical outcomes in infants with cystic fibrosis transmembrane conductance regulator (CFTR) related metabolic syndrome
    Clement L Ren
    Division of Pediatric Pulmonology, School of Medicine and Dentistry, University of Rochester, Rochester, New York, USA
    Pediatr Pulmonol 46:1079-84. 2011
  4. ncbi request reprint Changes in lung function measured by spirometry and the forced oscillation technique in cystic fibrosis patients undergoing treatment for respiratory tract exacerbation
    Clement L Ren
    Division of Pediatric Pulmonology, University of Rochester, Rochester, New York 14642, USA
    Pediatr Pulmonol 41:345-9. 2006
  5. ncbi request reprint Assessment and monitoring of cystic fibrosis lung disease in infants and young children
    Clement L Ren
    University of Rochester, Department of Pediatrics, 601 Elmwood Avenue, Rochester, NY 14642, USA
    Expert Rev Respir Med 2:381-90. 2008
  6. ncbi request reprint Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function
    Clement L Ren
    Department of Pediatrics, University of Rochester, Rochester, New York 14642, USA
    Pediatr Pulmonol 42:513-8. 2007
  7. ncbi request reprint Cystic fibrosis: evolution from a fatal disease of infancy with a clear phenotype to a chronic disease of adulthood with diverse manifestations
    Clement L Ren
    Division of Pediatric Pulmonology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA
    Clin Rev Allergy Immunol 35:97-9. 2008
  8. ncbi request reprint Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function
    Raj Padman
    Department of Pediatrics, Alfred I duPont Hospital for Children, Nemours Children s Clinic, Wilmington, DE 19899, USA
    Pediatrics 119:e531-7. 2007
  9. ncbi request reprint Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort
    Margaret Rosenfeld
    Department of Pediatrics, Seattle Children s Hospital and University of Washington, Seattle, Washington, USA
    Pediatr Pulmonol 45:934-44. 2010
  10. doi request reprint Relationship between inhaled corticosteroid therapy and rate of lung function decline in children with cystic fibrosis
    Clement L Ren
    Department of Pediatrics, University of Rochester, Rochester, NY, USA
    J Pediatr 153:746-51. 2008

Detail Information

Publications19

  1. pmc Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis
    Clement L Ren
    University of Rochester, Rochester, NY, USA
    J Cyst Fibros 11:293-9. 2012
    ..The goal of this study was to determine the association of multiple antibiotic-resistant Pseudomonas aeruginosa (MARPA) acquisition with lung function decline in patients with cystic fibrosis (CF)...
  2. doi request reprint Analysis of the associations between lung function and clinical features in preschool children with cystic fibrosis
    Clement L Ren
    University of Rochester, Rochester, New York 14642, USA
    Pediatr Pulmonol 47:574-81. 2012
    ..To analyze cross-sectional and longitudinal associations between lung function measures and clinical features in a cohort of preschool children with cystic fibrosis (CF)...
  3. doi request reprint Clinical outcomes in infants with cystic fibrosis transmembrane conductance regulator (CFTR) related metabolic syndrome
    Clement L Ren
    Division of Pediatric Pulmonology, School of Medicine and Dentistry, University of Rochester, Rochester, New York, USA
    Pediatr Pulmonol 46:1079-84. 2011
    ..Close initial monitoring of these patients is warranted. Pediatr. Pulmonol. 2011; 46:1079-1084. © 2011 Wiley Periodicals, Inc...
  4. ncbi request reprint Changes in lung function measured by spirometry and the forced oscillation technique in cystic fibrosis patients undergoing treatment for respiratory tract exacerbation
    Clement L Ren
    Division of Pediatric Pulmonology, University of Rochester, Rochester, New York 14642, USA
    Pediatr Pulmonol 41:345-9. 2006
    ..We speculate that FOT can serve as an alternative method to measure lung function in CF patients unable to perform spirometry, such as young children...
  5. ncbi request reprint Assessment and monitoring of cystic fibrosis lung disease in infants and young children
    Clement L Ren
    University of Rochester, Department of Pediatrics, 601 Elmwood Avenue, Rochester, NY 14642, USA
    Expert Rev Respir Med 2:381-90. 2008
    ..In this article, we will review these advances and techniques, and discuss future directions for research and clinical applications...
  6. ncbi request reprint Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function
    Clement L Ren
    Department of Pediatrics, University of Rochester, Rochester, New York 14642, USA
    Pediatr Pulmonol 42:513-8. 2007
    ..Similar results were seen in patients >or=18 years old. The results of our study highlight the growing clinical impact of MRSA infections in CF patients...
  7. ncbi request reprint Cystic fibrosis: evolution from a fatal disease of infancy with a clear phenotype to a chronic disease of adulthood with diverse manifestations
    Clement L Ren
    Division of Pediatric Pulmonology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA
    Clin Rev Allergy Immunol 35:97-9. 2008
    ..This issue of CRAI will review several areas of progress in our understanding and treatment of CF...
  8. ncbi request reprint Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function
    Raj Padman
    Department of Pediatrics, Alfred I duPont Hospital for Children, Nemours Children s Clinic, Wilmington, DE 19899, USA
    Pediatrics 119:e531-7. 2007
    ..The aim of this study was to assess whether patterns of care for infants at cystic fibrosis sites with superior average lung function in 6- to 12-year-old children showed any differences from those at the lowest outcome sites...
  9. ncbi request reprint Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort
    Margaret Rosenfeld
    Department of Pediatrics, Seattle Children s Hospital and University of Washington, Seattle, Washington, USA
    Pediatr Pulmonol 45:934-44. 2010
    ..The EPIC Observational Study is an ongoing prospective cohort study investigating risk factors for and clinical outcomes associated with early Pseudomonas aeruginosa (Pa) acquisition in young children with cystic fibrosis (CF)...
  10. doi request reprint Relationship between inhaled corticosteroid therapy and rate of lung function decline in children with cystic fibrosis
    Clement L Ren
    Department of Pediatrics, University of Rochester, Rochester, NY, USA
    J Pediatr 153:746-51. 2008
    ....
  11. doi request reprint Effect of azithromycin on pulmonary function in patients with cystic fibrosis uninfected with Pseudomonas aeruginosa: a randomized controlled trial
    Lisa Saiman
    Columbia University, Department of Pediatrics, 650 W 168th St, PH 4 West, Room 420, New York, NY 10032, USA
    JAMA 303:1707-15. 2010
    ..Azithromycin is recommended as therapy for cystic fibrosis (CF) patients with chronic Pseudomonas aeruginosa infection, but there has not been sufficient evidence to support the benefit of azithromycin in other patients with CF...
  12. ncbi request reprint Early childhood wheezing is associated with lower lung function in cystic fibrosis
    Clement L Ren
    Department of Pediatrics, University of Rochester, Rochester, New York
    Pediatr Pulmonol 49:745-50. 2014
    ..To study the association between wheezing in children with cystic fibrosis (CF) and lung function in later life...
  13. ncbi request reprint Diagnosis of cystic fibrosis
    Karen Z Voter
    Division of Pediatric Pulmonology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA
    Clin Rev Allergy Immunol 35:100-6. 2008
    ..In this article, we will review the indications for sweat testing, alternative techniques to diagnose CF, and the approach to patients with an ambiguous or indeterminate diagnosis of CF...
  14. ncbi request reprint Use of modulators of airways inflammation in patients with CF
    Clement L Ren
    Division of Pediatric Pulmonology and Allergy, University of Rochester, Box 667, 601 Elmwood Ave, Rochester, NY 14642, USA
    Clin Rev Allergy Immunol 23:29-39. 2002
    ..In summary, numerous anti-inflammatory therapies have been applied to CF lung disease, but more large, well-controlled studies will need to be performed to determine their true clinical usefulness...
  15. ncbi request reprint Pulmonary function in technology-dependent children 2 years and older with bronchopulmonary dysplasia
    Isaac Talmaciu
    Division of Pediatric Pulmonology, St Christopher s Hospital For Children, Philadelphia, Pennsylvania, USA
    Pediatr Pulmonol 33:181-8. 2002
    ..We speculate that measurements of lung elastic recoil and tests of distribution of ventilation and pulmonary perfusion may be more sensitive in differentiating normoxemic and hypoxemic children with BPD 2 years and older...
  16. ncbi request reprint Trends in the clinical characteristics of the U.S. cystic fibrosis patient population from 1995 to 2005
    Donald R VanDevanter
    ICON Clinical Research, San Francisco, California, USA
    Pediatr Pulmonol 43:739-44. 2008
    ..Additionally, changes in these variables over the past decade may provide insight into the improving health of the CF population...
  17. ncbi request reprint Pulmonary manifestations in deltaF508/R117H
    Clement L Ren
    Pediatrics 119:647; author reply 647-8. 2007
  18. ncbi request reprint Comment on Sagel et al
    Clement L Ren
    Pediatr Pulmonol 40:275; author reply 276. 2005
  19. ncbi request reprint What is the best way to measure lung function?
    Clement L Ren
    Chest 123:667-8. 2003