Terry Robinson
Academic Appointments
- Associate Professor - Med Center Line, Pediatrics - Pulmonary Medicine
- Member, Child Health Research Institute
Key Documents
Contact Information
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Clinical Offices
Respiratory Specialties and ENT 730 Welch Rd 1st Floor Palo Alto, CA 94304 Tel Work (650) 497-8841 Fax (650) 497-8791Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
- Academic Offices
Personal Information EmailAlternate Contact Linda Young Administrative Assistant Email Tel Work 650-723-8325Not for medical emergencies or patient use
Professional Overview
Clinical Focus
- Pediatric Pulmonary
- Pulmonary Medicine/Cystic Fibrosis, Pediatric
Administrative Appointments
- Medical Specialties Peer Review Committee, LPCH (2005 - 2007)
- Packard Children's Hospital Resident Education Committee, LPCH (2001 - 2002)
Honors and Awards
- Provider of the Year, Cystic Fibrosis Foundation, Northern California Chapter (October 2006)
- Honorary Invited Participant, Leuven, Belgium, European Respiratory Society (February 2007)
- Honorary Invited Speaker Annual Scientific Meeting, Sydney, Australia, Auckland, New Zealand,, The Thoracic Society of Australia & New Zealand and ANZSRS (March 2007)
Professional Education
| Fellowship: | Stanford University School of Medicine CA (1997) |
| Residency: | Stanford University School of Medicine CA (1993) |
| Internship: | Stanford University School of Medicine CA (1991) |
| Board Certification: | Pediatric Pulmonary, American Board of Pediatrics (2002) |
| Medical Education: | Brown University Program RI (1990) |
Scientific Focus
Current Research Interests
My research interests focus on detection of early and progressive Cystic fibrosis (CF) structural lung disease by utilizing chest CT imaging and CT post-processing methodology. Current research efforts involve utilization of low dose infant & children CT imaging protocols and quantitative airway and air trapping algorithms to evaluate early and progressive CF disease. Additional areas of research in our laboratory include defining more direct pulmonary outcome measures to evaluate treatment effects in chronic diseases such as cystic fibrosis and pulmonary alveolar proteinosis.
Publications
- 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 disease. J Digit Imaging. 2010; (6): 744-54
- An airway phantom to standardize CT acquisition in multicenter clinical trials. Acad Radiol. 2009; (9): 1134-41
- Cystic fibrosis HRCT scores correlate strongly with Pseudomonas infection. Pediatr Pulmonol. 2009; (11): 1107-17
- Quantitative analysis of longitudinal response to aerosolized granulocyte-macrophage colony-stimulating factor in two adolescents with autoimmune pulmonary alveolar proteinosis. Chest. 2009; (3): 842-8
- Sampling density for the quantitative evaluation of air trapping. Pediatr Radiol. 2009; (3): 221-5
- Successful pregnancy and cesarean delivery via noninvasive ventilation in mitochondrial myopathy. J Perinatol. 2009; (2): 166-7
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