Terry E Robinson
Affiliation: Stanford University
- Cystic fibrosis HRCT scores correlate strongly with Pseudomonas infectionTerry E Robinson
Center of Excellence for Pediatric Cystic Fibrosis and Pulmonary Diseases, Stanford University Medical Center, Palo Alto, California 94305 5715, USA
Pediatr Pulmonol 44:1107-17. 2009....
- An airway phantom to standardize CT acquisition in multicenter clinical trialsTerry E Robinson
Center of Excellence for Pulmonary Biology, Division of Pediatric Pulmonary, Stanford University Medical Center, 770 Welch Road, Suite 350, Palo Alto, CA 94305 5715, USA
Acad Radiol 16:1134-41. 2009..The purpose of this study was to demonstrate the use of a phantom to standardize low-dose chest computed tomographic (CT) protocols in children with cystic fibrosis...
- Quantitative analysis of longitudinal response to aerosolized granulocyte-macrophage colony-stimulating factor in two adolescents with autoimmune pulmonary alveolar proteinosisTerry E Robinson
Center of Excellence in Pulmonary Biology, Division of Pediatric Pulmonary, Stanford University Medical Center, 770 Welch Road, Stanford, CA 94305 5715, USA
Chest 135:842-8. 2009..Aerosolized GM-CSF therapy (aeroGM-SCF) has qualitatively improved the clinical condition of patients with APAP. This report details quantitative chest CT responses to aeroGM-CSF...
- Computed tomography scanning techniques for the evaluation of cystic fibrosis lung diseaseTerry E Robinson
Center of Excellence for Pulmonary Biology, Division of Pediatric Pulmonary, Stanford University School of Medicine, Palo Alto, California 94305 5715, USA
Proc Am Thorac Soc 4:310-5. 2007....
- Imaging of the chest in cystic fibrosisTerry E Robinson
Department of Pediatrics, Center of Excellence in Pulmonary Biology Pulmonary Division, Stanford University Medical Center, 770 Welch Road, Palo Alto, CA 94304 5715, USA
Clin Chest Med 28:405-21. 2007..This article covers current chest imaging modalities. It discusses CT, the research modality most commonly used to assess lung disease in CF, new insights regarding CF lung disease, and future directions in research and clinical care...
- Dornase alfa reduces air trapping in children with mild cystic fibrosis lung disease: a quantitative analysisTerry E Robinson
Department of Pediatrics Pulmonary, Pediatric Pulmonary Division, Stanford University Medical Center, 701 Welch Rd, Whelan Building, 3328, Palo Alto, CA 94305 5786, USA
Chest 128:2327-35. 2005....
- High-resolution CT scanning: potential outcome measureTerry E Robinson
Pediatric Pulmonary Division, Stanford University Medical Center, Palo Alto, California 94305 5786, USA
Curr Opin Pulm Med 10:537-41. 2004..The purpose of this review is to summarize recent developments in HRCT and volumetric chest CT imaging, CF chest CT scoring systems, and review how HRCT/volumetric CT can provide useful outcome measures for future CF clinical research...
- Composite spirometric-computed tomography outcome measure in early cystic fibrosis lung diseaseTerry E Robinson
Pediatric Pulmonary Division, Stanford University Medical Center, 701 Welch Road, Whelan Building 3328, Palo Alto, CA 94304 5786
Am J Respir Crit Care Med 168:588-93. 2003....
- Sampling density for the quantitative evaluation of air trappingMichael L Goris
Division of Nuclear Medicine H0101, Stanford University School of Medicine, Stanford, CA, 94305 5281, USA
Pediatr Radiol 39:221-5. 2009..To reduce the dose one can change the CT acquisition settings or decrease the sampling density...
- Development and validation of automated 2D-3D bronchial airway matching to track changes in regional bronchial morphology using serial low-dose chest CT scans in children with chronic lung diseasePavithra Raman
Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305 5105, USA
J Digit Imaging 23:744-54. 2010..01) and was as accurate as manual matching, allowing efficient comparison of airways obtained on low-dose spiral CT imaging with low-dose HRCT scans...
- A critical discussion of computer analysis in medical imagingMichael L Goris
Division of Nuclear Medicine, Stanford University School of Medicine, Stanford, CA 94305 5281, USA
Proc Am Thorac Soc 4:347-9. 2007..However, in the context of trials, the validation may come from a superior ability to detect objective change and to discriminate between affected and unaffected individuals...
- Acute stress disorder following ventilationRichard J Shaw
Division of Child Psychiatry, Stanford University School of Medicine, 401 Quarry Road, Stanford, CA 94305-5719, USA
Psychosomatics 43:74-6. 2002
- An automated approach to quantitative air trapping measurements in mild cystic fibrosisMichael L Goris
Division of Nuclear Medicine Radiology, Stanford University, CA 94305, USA
Chest 123:1655-63. 2003..To automatically derive the degree of air trapping in mild cystic fibrosis (CF) disease from high-resolution CT (HRCT) data, and to evaluate the discriminating power of the measurement...
- Fully automated system for three-dimensional bronchial morphology analysis using volumetric multidetector computed tomography of the chestRaman Venkatraman
Department of Pediatric Pulmonology, Stanford University School of Medicine, Stanford, CA 94305, USA
J Digit Imaging 19:132-9. 2006....
- Computed tomography in the evaluation of cystic fibrosis lung diseaseAlan S Brody
Department of Radiology, MLC 5031, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229 3039, USA
Am J Respir Crit Care Med 172:1246-52. 2005..Second is the need for more sensitive outcome measures to assess new therapies. This had led to new interest and a series of important publications. The goal of this article is to present the current status of CT scanning in CF...
- Quantitative air-trapping analysis in children with mild cystic fibrosis lung diseaseAnne-Sophie Bonnel
Division of Pediatric Respirology, University Hospital, Rouen, France
Pediatr Pulmonol 38:396-405. 2004..Pulmonary density measurements and % AT better discriminated differences between groups than PFTs. Measurements made on expiratory scans near FRC showed significantly higher values for AT than those made near RV...
- Phenotypic and genetic characterization of patients with features of "nonclassic" forms of cystic fibrosisJoshua D Groman
Cyctic Fibrosis Foundation Genotyping Center and McKusick Nathans Institute of Genetic Medicine, Bloomberg School of Public Health, Johns Hopkins University School of Medicine, 733 N Broadway, Baltimore, MD 21287, USA
J Pediatr 146:675-80. 2005....
- Estimation of the radiation dose from CT in cystic fibrosisPim A de Jong
Chest 133:1289-91; author reply 1290-1. 2008