
Dr. Carlos Eduardo Milla MD
Pulmonologist (Pediatric) | Pediatric Pulmonology
770 Welch Rd Suite 350 Palo Alto CA, 94304About
Dr. Carlos Milla practices Pediatric Pulmonology in Palo Alto, CA. Dr. Milla treats children who have breathing problems, or a problem with his or her lungs. Pediatric pulmonologists often treat children with chronic cough, difficulty breathing, recurring pneumonia, asthma, cystic fibrosis, apnea, chronic lung disease in premature infants, noisy breathing, and conditions that require special equipment to monitor and/or help with breathing at home.
Education and Training
Universidad Peruana Cayetano Heredia Facultad de Medicina Alberto Hurtado 1986
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Allergic bronchopulmonary aspergillosis and cystic fibrosis.
- Long-term effects of aerosolised rhDNase on pulmonary disease progression in patients with cystic fibrosis.
- Recombinant human DNase in cystic fibrosis.
- Randomized, controlled trial of low-dose inhaled nitric oxide in the treatment of term and near-term infants with respiratory failure and pulmonary hypertension.
- Trends in pulmonary function in patients with cystic fibrosis correlate with the degree of glucose intolerance at baseline.
- Continuous propofol infusion in 142 critically ill children.
- Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis.
- High-frequency chest compression: effect of the third generation compression waveform.
- Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis.
- Association of nutritional status and pulmonary function in children with cystic fibrosis.
- Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis.
- Cystic fibrosis pulmonary exacerbations.
- Inflammatory cytokines and the development of pulmonary complications after allogeneic hematopoietic cell transplantation in patients with inherited metabolic storage disorders.
- Different frequencies should be prescribed for different high frequency chest compression machines.
- Nutrition and lung disease in cystic fibrosis.
Treatments
- Asthma
- Sleep Apnea
- Cerebral Palsy
- Pulmonary Hypertension
- Bronchiectasis
- Chronic Obstructive Pulmonary Disease (copd)
- Cystic Fibrosis (cf)
- Obstructive Sleep Apnea (osa)
Publications
- American jourl of respiratory and critical care medicineMutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype.2014
- Anls of the American Thoracic SocietyStandardizing sal nitric oxide measurement as a test for primary ciliary dyskinesia.2013
- Current opinion in pediatricsCystic fibrosis in the era of genomic medicine.2013
- AMERICAN JOURL OF HUMAN GENETICSExome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia2013
- The Jourl of molecular diagnostics : JMDNovel CFTR Variants Identified during the First 3 Years of Cystic Fibrosis Newborn Screening0
- SCIENCE TRANSLATIOL MEDICINEQuantitative Alysis of the Human Airway Microbial Ecology Reveals a Perv2012
- OTOLARYNGOLOGY-HEAD AND NECK SURGERYEffect of Endoscopic Sinus Surgery on Pulmory Status of Adults with Cystic Fibrosis2012
- PAEDIATRIC RESPIRATORY REVIEWSPulmory Complications of Endocrine and Metabolic Disorders2012
- PEDIATRIC PULMONOLOGYDiagnostic Yield of sal Scrape Biopsies in Primary Ciliary Dyskinesia: A Multicenter Experience2011
- Pediatric pulmonologyDiagnostic yield of sal scrape biopsies in primary ciliary dyskinesia: A multicenter experience.0
- JOURL OF CYSTIC FIBROSISCharacteristics of gastroesophageal reflux in adults with cystic fibrosis2010
- BONE MARROW TRANSPLANTATIONPre-transplant risk factors affecting outcome in Hurler syndrome2010
- RESPIRATORY CAREComparison of Settings Used for High-Frequency Chest-Wall Compression in Cystic Fibrosis2010
- SEMIRS IN RESPIRATORY AND CRITICAL CARE MEDICINENutrition in Cystic Fibrosis2009
- PAEDIATRIC RESPIRATORY REVIEWSCystic fibrosis related diabetes2009
- PEDIATRIC PULMONOLOGYLongitudil Assessment of Lung Function From Infancy to Childhood in Patients With Cystic Fibrosis2009
- PEDIATRIC PULMONOLOGYAssociations of Psychosocial Factors With Health Outcomes Among Youth With Cystic Fibrosis2009
- PEDIATRIC PULMONOLOGYSteroid-sparing effect of Omalizumab for allergic bronchopulmory aspergillosis and cystic fibrosis2008
- JOURL OF CYSTIC FIBROSISGender differences in treatment adherence among youth with cystic fibrosis2008
- CHESTComparison of high-frequency chest wall oscillation with differing waveforms for airway clearance2007
- DIGESTIVE DISEASES AND SCIENCESHepatolithiasis and Cholangiocarcinoma in cystic fibrosis2007
- HUMAN GENE THERAPYRepeated aerosolized AAV-CFTR for treatment of cystic fibrosis2007
- CLINICS IN CHEST MEDICINENutrition and lung disease in cystic fibrosis2007
- DIABETES CAREMicrovascular complications in cystic fibrosis-related diabetes2007
- PEDIATRIC PULMONOLOGYMicrobiology, safety2006
- Biomedical instrumentation & technologyDifferent frequencies should be prescribed for different high frequency chest compression machines.2006
- BIOLOGY OF BLOOD AND MARROW TRANSPLANTATIONInflammatory cytokines2006
- JOURL OF PEDIATRICSCystic fibrosis pulmory exacerbations2006
- DIABETES CAREDiabetes is associated with dramatically decreased survival2005
- AMERICAN JOURL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYAbsence of host tumor necrosis factor receptor 1 attenuates manifestations of idiopathic pneumonia2005
- PEDIATRIC PULMONOLOGYSafety and tolerability of denufosol tetrasodium inhalation solution2005
- AMERICAN JOURL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYAltered airway responsiveness in CD38-deficient mice2005
- BIOLOGY OF BLOOD AND MARROW TRANSPLANTATIONtural history of pulmory complications in children after bone marrow transplantation2005
- METABOLISM-CLINICAL AND EXPERIMENTALInsulin regulation of free fatty acid kinetics2004
- CURRENT OPINION IN PULMORY MEDICINEAssociation of nutritiol status and pulmory function in children with cystic fibrosis2004
- AMERICAN JOURL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYMyeloperoxidase deficiency enhances inflammation after allogeneic marrow transplantation2004
- JOURL OF LABORATORY AND CLINICAL MEDICINEPeroxidase activity within circulating neutrophils correlates with pulmory phenotype2004
- jourl of allergy and clinical immunologyMethodologic advancements in the study of airway smooth muscle.2004
- Biomedical instrumentation & technologyHigh-frequency chest compression: effect of the third generation compression waveform.2004
- CHESTRepeated adeno-associated virus serotype 2 aerosol2004
- AMERICAN JOURL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYSurfactant protein A is a required mediator of keratinocyte growth factor after experimental marrow2003
- PEDIATRICSLongitudil changes in growth parameters are correlated with changes in pulmory function in children2003
- JOURL OF HEART AND LUNG TRANSPLANTATIONSafety of inhaled nitric oxide after lung transplantation2003
- Pediatric diabetesInsulin glargine improves hemoglobin A1c in children2003
- JOURL OF PEDIATRICSAbnormal glucose tolerance in cystic fibrosis: Why should patients be screened?2003
- PEDIATRICSContinuous propofol infusion in 142 critically ill children2002
- AMERICAN JOURL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYSurfactant protein A decreases lung injury and mortality after murine marrow transplantation2002
- AMERICAN JOURL OF CLINICAL NUTRITIONAbnormal lipid concentrations in cystic fibrosis2002
- AMERICAN JOURL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYEffects of oxidant stress on inflammation2001
- DIABETES CAREInsulin and glucose excursion following premeal insulin lispro or repaglinide in cystic fibrosis2001
- DIABETESProtein metabolism in clinically stable adult cystic fibrosis patients with abnormal glucose2001
- AMERICAN JOURL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYHuman surfactant protein A suppresses T cell-dependent inflammation2001
- Milla, C. E., Warwick, W. J., Moran, A.Trends in pulmory function in patients with cystic fibrosis correlate with the degree of glucose2000
- Cornfield, D. N., Mayrd, R. C., deRegnier, R. A., Guiang, S. F., BarbaRandomized, controlled trial of low-dose inhaled nitric oxide in the treatment of term and near1999
- LANCETRecombint human Dse in cystic fibrosis1999
- AMERICAN JOURL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYNO causes perital pulmory vasodilation through K+-channel activation and intracellular Ca2+ release1999
- AMERICAN JOURL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYHigh levels of peroxynitrite are generated1999
- PEDIATRIC PULMONOLOGYAllergic bronchopulmory aspergillosis and cystic fibrosis1999
- THORAXLong term effects of aerosolised rhDse on pulmory disease progression1998
- CIRCULATIONEffects of inhaled nitric oxide and oxygen in high-altitude pulmory edema1998
- CHESTRisk of death in cystic fibrosis patients with severely compromised lung function1998
- AMERICAN JOURL OF RESPIRATORY AND CRITICAL CARE MEDICINEPCR ribotyping and endonuclease subtyping in the epidemiology of Burkholderia cepacio infection1997
- JOURL OF PARENTERAL AND ENTERAL NUTRITIONGlycemic response to dietary supplements1996
- PEDIATRIC PULMONOLOGYClinical significance of the recovery of Aspergillus species from the respiratory secretions of1996
- LANCETHIGH-STRENGTH PANCREATIC-ENZYMES1994
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Nearest Hospitals
LUCILE SALTER PACKARD CHILDREN'S HSP AT STANFORDl
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570 WILLOW ROAD MENLO PARK CA 94025