Carlos Milla
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) 724-4788 Fax (650) 497-8791Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
- Academic Offices
Personal Information Email Tel (650) 736-9824 Tel (650) 723-8325Alternate Contact Linda Young Administrative Associate Email Tel Work 650-723-8325Not for medical emergencies or patient use
Professional Overview
Clinical Focus
- Pediatric Pulmonary
- Cystic Fibrosis
- Primary Ciliary Dyskinesia
- Bronchopulmonary Dysplasia
- Pulmonary Hypertension
- Rare Lung Diseases
Administrative Appointments
- Director, The Stanford Cystic Fibrosis Center (2009 - present)
Honors and Awards
- Crandall Endowed Scholar in Pediatric Pulmonary Medicine, Stanford University School of Medicine (2007)
- Annalisa Marzotto Endowed Chair in Cystic Fibrosis Care, University of Minnesota Medical School (2005)
Professional Education
| Internship: | SUNY at Brooklyn School Of Medicine NY (1990) |
| Residency: | SUNY at Brooklyn School Of Medicine NY (1992) |
| Board Certification: | Pediatric Pulmonary, American Board of Pediatrics (1996) |
| Fellowship: | University of Minnesota School of Medicine MN (1995) |
| Medical Education: | Universidad Peruana Cayetano Heredia, APDO 5045 Peru (1986) |
Graduate & Fellowship Program Affiliations
Scientific Focus
Current Research Interests
My research interests have centered on the inflammatory responses that lead to airway disease in Cystic Fibrosis (CF) and the metabolic factors that contribute to CF lung disease progression. Current efforts are focused on the understanding of the early events that drive the development of lung disease through the study of infants with CF identified by newborn screening. This includes the development of new diagnostic tools that permit the early detection of lung disease manifestations.
Clinical Trials
- Recruiting Early Intervention in Cystic Fibrosis Exacerbation
- Recruiting Study to Evaluate the Effect of KB001-A on Time-to-Need for Antibiotic Treatment
- Recruiting Long-term Study in US Cystic Fibrosis Patients Receiving Digestive Enzyme Supplements to Assess Any Narrowing of the Large Intestine Causing Adverse Intestinal Symptoms (Fibrosing Colonopathy)
- Recruiting Rare Genetic Disorders of the Breathing Airways
Publications
- Cystic fibrosis in the era of genomic medicine. Curr Opin Pediatr. 2013; (3): 323-8
- Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia. Am J Hum Genet. 2013; (1): 99-106
- Effect of endoscopic sinus surgery on pulmonary status of adults with cystic fibrosis. Otolaryngol Head Neck Surg. 2012; (3): 557-62
- Pulmonary complications of endocrine and metabolic disorders. Paediatr Respir Rev. 2012; (1): 23-8
- Quantitative analysis of the human airway microbial ecology reveals a pervasive signature for cystic fibrosis. Sci Transl Med. 2012; (153): 153ra130
- Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: A multicenter experience. Pediatr Pulmonol. 2011
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