Carlos Milla

Associate Professor of Pediatrics (Pulmonary Medicine) at the Lucile Salter Packard Children's Hospital

Professional Education

Board Certification: Pediatric Pulmonary, American Board of Pediatrics (1996)

Medical Education: Universidad Peruana Cayetano Heredia (1986) Peru

Internship: SUNY at Brooklyn School Of Medicine (1990) NY

Residency: SUNY at Brooklyn School Of Medicine (1992) NY

Fellowship: University of Minnesota School of Medicine (1995) MN

Honors & 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)

Administrative Appointments

Director, The Stanford Cystic Fibrosis Center (2009 - Present)

Clinical Trials

Clinical trials are research studies that evaluate a new medical approach, device, drug, or other treatment. As a Stanford Health Care patient, you have access to the latest, advanced clinical trials.

Open trials refer to studies currently accepting participants. Closed trials are not currently enrolling, but may open in the future.

Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype
Knowles, M. R., Ostrowski, L. E., Leigh, M. W., Sears, P. R., Davis, S. D., & Zariwala, M. A. (2014). Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 189(6), 707-717.

Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.
Leigh, M. W., Hazucha, M. J., Chawla, K. K., Baker, B. R., Shapiro, A. J., & Knowles, M. R. (2013). Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia. Annals of the American Thoracic Society, 10(6), 574-581.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
Austin-Tse, C., Halbritter, J., Zariwala, M. A., Gilberti, R. M., Gee, H. Y., & Hildebrandt, F. (2013). Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia. AMERICAN JOURNAL OF HUMAN GENETICS, 93(4), 672-686.

Cystic fibrosis in the era of genomic medicine.
Milla, C. E. (2013). Cystic fibrosis in the era of genomic medicine. Current opinion in pediatrics, 25(3), 323-328.

Exome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia
Knowles, M. R., Leigh, M. W., Ostrowski, L. E., Huang, L., Carson, J. L., & Zariwala, M. A. (2013). Exome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia. AMERICAN JOURNAL OF HUMAN GENETICS, 92(1), 99-106.

Novel CFTR Variants Identified during the First 3 Years of Cystic Fibrosis Newborn Screening in California.
Prach, L., Koepke, R., Kharrazi, M., Keiles, S., & Salinas, D. B. (2013). Novel CFTR Variants Identified during the First 3 Years of Cystic Fibrosis Newborn Screening in California. The Journal of molecular diagnostics : JMD.

Quantitative Analysis of the Human Airway Microbial Ecology Reveals a Pervasive Signature for Cystic Fibrosis
Blainey, P. C., Milla, C. E., Cornfield, D. N., & Quake, S. R. (2012). Quantitative Analysis of the Human Airway Microbial Ecology Reveals a Pervasive Signature for Cystic Fibrosis. SCIENCE TRANSLATIONAL MEDICINE, 4(153).

Effect of Endoscopic Sinus Surgery on Pulmonary Status of Adults with Cystic Fibrosis
Kempainen, R. R., Sajan, J. A., Pylkas, A. M., Dunitz, J. M., Rimell, F. L., & Milla, C. E. (2012). Effect of Endoscopic Sinus Surgery on Pulmonary Status of Adults with Cystic Fibrosis. OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 147(3), 557-562.

Pulmonary Complications of Endocrine and Metabolic Disorders
Milla, C. E., & Zirbes, J. (2012). Pulmonary Complications of Endocrine and Metabolic Disorders. PAEDIATRIC RESPIRATORY REVIEWS, 13(1), 23-28.

Diagnostic Yield of Nasal Scrape Biopsies in Primary Ciliary Dyskinesia: A Multicenter Experience
Olin, J. T., Burns, K., Carson, J. L., Metjian, H., Atkinson, J. J., & Sagel, S. D. (2011). Diagnostic Yield of Nasal Scrape Biopsies in Primary Ciliary Dyskinesia: A Multicenter Experience. PEDIATRIC PULMONOLOGY, 46(5), 483-488.

Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: A multicenter experience.
Olin, J. T., Burns, K., Carson, J. L., Metjian, H., & Atkinson, J. J. (2011). Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: A multicenter experience. Pediatric pulmonology.

Characteristics of gastroesophageal reflux in adults with cystic fibrosis
Sabati, A. A., Kempainen, R. R., Milla, C. E., Ireland, M., Schwarzenberg, S. J., & Khan, K. M. (2010). Characteristics of gastroesophageal reflux in adults with cystic fibrosis. JOURNAL OF CYSTIC FIBROSIS, 9(5), 365-370.

Pre-transplant risk factors affecting outcome in Hurler syndrome
Orchard, P. J., Milla, C., Braunlin, E., DeFor, T., Bjoraker, K., & Tolar, J. (2010). Pre-transplant risk factors affecting outcome in Hurler syndrome. BONE MARROW TRANSPLANTATION, 45(7), 1239-1246.

Comparison of Settings Used for High-Frequency Chest-Wall Compression in Cystic Fibrosis
Kempainen, R. R., Milla, C., Dunitz, J., Savik, K., Hazelwood, A., & Billings, J. L. (2010). Comparison of Settings Used for High-Frequency Chest-Wall Compression in Cystic Fibrosis. RESPIRATORY CARE, 55(6), 695-701.

Nutrition in Cystic Fibrosis
Matel, J. L., & Milla, C. E. (2009). Nutrition in Cystic Fibrosis. SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 30(5), 579-586.

Cystic fibrosis related diabetes
Zirbes, J., & Milla, C. E. (2009). Cystic fibrosis related diabetes. PAEDIATRIC RESPIRATORY REVIEWS, 10(3), 118-123.

Longitudinal Assessment of Lung Function From Infancy to Childhood in Patients With Cystic Fibrosis
Harrison, A. N., Regelmann, W. E., Zirbes, J. M., & Milla, C. E. (2009). Longitudinal Assessment of Lung Function From Infancy to Childhood in Patients With Cystic Fibrosis. PEDIATRIC PULMONOLOGY, 44(4), 330-339.

Associations of Psychosocial Factors With Health Outcomes Among Youth With Cystic Fibrosis
Patterson, J. M., Wall, M., Berge, J., & Milla, C. (2009). Associations of Psychosocial Factors With Health Outcomes Among Youth With Cystic Fibrosis. PEDIATRIC PULMONOLOGY, 44(1), 46-53.

Steroid-sparing effect of Omalizumab for allergic bronchopulmonary aspergillosis and cystic fibrosis
Zirbes, J. M., & Milla, C. E. (2008). Steroid-sparing effect of Omalizumab for allergic bronchopulmonary aspergillosis and cystic fibrosis. PEDIATRIC PULMONOLOGY, 43(6), 607-610.

Gender differences in treatment adherence among youth with cystic fibrosis: Development of a new questionnaire
Patterson, J. M., Wall, M., Berge, J., & Milla, C. (2008). Gender differences in treatment adherence among youth with cystic fibrosis: Development of a new questionnaire. JOURNAL OF CYSTIC FIBROSIS, 7(2), 154-164.

Comparison of high-frequency chest wall oscillation with differing waveforms for airway clearance in cystic fibrosis
Kempainen, R. R., Williams, C. B., Hazelwood, A., Rubin, B. K., & Milla, C. E. (2007). Comparison of high-frequency chest wall oscillation with differing waveforms for airway clearance in cystic fibrosis. CHEST, 132(4), 1227-1232.

Hepatolithiasis and Cholangiocarcinoma in cystic fibrosis: A case series and review of the literature
Perdue, D. G., Cass, O. W., Milla, C., Dunitz, J., Jessurun, J., & Schwarzenberg, S. J. (2007). Hepatolithiasis and Cholangiocarcinoma in cystic fibrosis: A case series and review of the literature. DIGESTIVE DISEASES AND SCIENCES, 52(10), 2638-2642.

Repeated aerosolized AAV-CFTR for treatment of cystic fibrosis: A Randomized placebo-controlled phase 2B trial
Moss, R. B., Milla, C., Colombo, J., Accurso, F., Zeitlin, P. L., & Heald, A. E. (2007). Repeated aerosolized AAV-CFTR for treatment of cystic fibrosis: A Randomized placebo-controlled phase 2B trial. HUMAN GENE THERAPY, 18(8), 726-732.

Nutrition and lung disease in cystic fibrosis
Milla, C. E. (2007). Nutrition and lung disease in cystic fibrosis. CLINICS IN CHEST MEDICINE, 28(2), 319-?.

Microvascular complications in cystic fibrosis-related diabetes
Schwarzenberg, S. J., Walk, D., Thomas, W., Milla, C., Olsen, T. W., & Grover, T. (2007). Microvascular complications in cystic fibrosis-related diabetes. DIABETES CARE, 30(5), 1056-1061.

Microbiology, safety, and pharmacokinetics of aztreonam lysinate for inhalation in patients with cystic fibrosis
Gibson, R. L., Retsch-Bogart, G. Z., Oermann, C., Milla, C., Pilewski, J., & Burns, J. L. (2006). Microbiology, safety, and pharmacokinetics of aztreonam lysinate for inhalation in patients with cystic fibrosis. PEDIATRIC PULMONOLOGY, 41(7), 656-665.

Different frequencies should be prescribed for different high frequency chest compression machines.
Milla, C. E., Hansen, L. G., & Warwick, W. J. (2006). Different frequencies should be prescribed for different high frequency chest compression machines. Biomedical instrumentation & technology , 40(4), 319-324.

Inflammatory cytokines and the development of pulmonary complications after allogeneic hematopoietic cell transplantation in patients with inherited metabolic storage disorders
Kbarbanda, S., Panoskaltsis-Mortari, A., Haddad, I. Y., Blazar, B. R., Orchard, P. J., & Baker, K. S. (2006). Inflammatory cytokines and the development of pulmonary complications after allogeneic hematopoietic cell transplantation in patients with inherited metabolic storage disorders. BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 12(4), 430-437.

Cystic fibrosis pulmonary exacerbations
Ferkol, T., Rosenfeld, M., & Milla, C. E. (2006). Cystic fibrosis pulmonary exacerbations. JOURNAL OF PEDIATRICS, 148(2), 259-264.

Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis
Milla, C. E., Billings, J., & Moran, A. (2005). Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis. DIABETES CARE, 28(9), 2141-2144.

Absence of host tumor necrosis factor receptor 1 attenuates manifestations of idiopathic pneumonia syndrome
Shukla, M., Yang, S. X., Milla, C., Panoskaltsis-Mortari, A., Blazar, B. R., & Haddad, I. Y. (2005). Absence of host tumor necrosis factor receptor 1 attenuates manifestations of idiopathic pneumonia syndrome. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 288(5), L942-L949.

Safety and tolerability of denufosol tetrasodium inhalation solution, a novel P2Y(2) receptor agonist: Results of a phase 1/phase 2 multicenter study in mild to moderate cystic fibrosis
Deterding, R., Retsch-Bogart, G., Milgram, L., Gibson, R., Daines, C., & Ramsey, B. (2005). Safety and tolerability of denufosol tetrasodium inhalation solution, a novel P2Y(2) receptor agonist: Results of a phase 1/phase 2 multicenter study in mild to moderate cystic fibrosis. PEDIATRIC PULMONOLOGY, 39(4), 339-348.

Altered airway responsiveness in CD38-deficient mice
Deshpande, D. A., White, T. A., Guedes, A. Gp., Milla, C., Walseth, T. F., & Kannan, M. S. (2005). Altered airway responsiveness in CD38-deficient mice. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 32(2), 149-156.

Natural history of pulmonary complications in children after bone marrow transplantation
Eikenberry, M., Bartakova, H., DeFor, T., Haddad, I. Y., Ramsay, N. Kc., & Cornfield, D. N. (2005). Natural history of pulmonary complications in children after bone marrow transplantation. BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 11(1), 56-64.

Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance
Moran, A., Basu, R., Milla, C., & Jensen, M. D. (2004). Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance. METABOLISM-CLINICAL AND EXPERIMENTAL, 53(11), 1467-1472.

Association of nutritional status and pulmonary function in children with cystic fibrosis
Milla, C. E. (2004). Association of nutritional status and pulmonary function in children with cystic fibrosis. CURRENT OPINION IN PULMONARY MEDICINE, 10(6), 505-509.

Myeloperoxidase deficiency enhances inflammation after allogeneic marrow transplantation
Milla, C., Yang, S. X., Cornfield, D. N., Brennan, M. L., Hazen, S. L., & Haddad, I. Y. (2004). Myeloperoxidase deficiency enhances inflammation after allogeneic marrow transplantation. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 287(4), L706-L714.

Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis
Garner, H. P., PHILLIPS, J. R., Herron, J. G., Severson, S. J., Milla, C. E., & Regelmann, W. E. (2004). Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis. JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 144(3), 127-133.

Methodologic advancements in the study of airway smooth muscle.
Kotlikoff, M. I., Kannan, M. S., Solway, J., Deng, K.-Y., Deshpande, D. A., & Woodruff, P. G. (2004). Methodologic advancements in the study of airway smooth muscle. journal of allergy and clinical immunology, 114(2), S18-31.

High-frequency chest compression: effect of the third generation compression waveform.
Milla, C. E., Hansen, L. G., Weber, A., & Warwick, W. J. (2004). High-frequency chest compression: effect of the third generation compression waveform. Biomedical instrumentation & technology , 38(4), 322-328.

Repeated adeno-associated virus serotype 2 aerosol-mediated cystic fibrosis transmembrane regulator gene transfer to the lungs of patients with cystic fibrosis - A multicenter, double-blind, placebo-controlled trial
Moss, R. B., Rochman, D., Spencer, L. T., Aitken, M. L., Zeitlhi, P. L., & Heald, A. E. (2004). Repeated adeno-associated virus serotype 2 aerosol-mediated cystic fibrosis transmembrane regulator gene transfer to the lungs of patients with cystic fibrosis - A multicenter, double-blind, placebo-controlled trial. CHEST, 125(2), 509-521.

Surfactant protein A is a required mediator of keratinocyte growth factor after experimental marrow transplantation
Haddad, I. Y., Milla, C., Yang, S. X., Panoskaltsis-Mortari, A., Hawgood, S., & Blazar, B. R. (2003). Surfactant protein A is a required mediator of keratinocyte growth factor after experimental marrow transplantation. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 285(3), L602-L610.

Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis
Peterson, M. L., Jacobs, D. R., & Milla, C. E. (2003). Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis. PEDIATRICS, 112(3), 588-592.

Safety of inhaled nitric oxide after lung transplantation
Cornfield, D. N., Milla, C. E., Haddad, I. Y., Barbato, J. E., & Park, S. J. (2003). Safety of inhaled nitric oxide after lung transplantation. JOURNAL OF HEART AND LUNG TRANSPLANTATION, 22(8), 903-907.

Insulin glargine improves hemoglobin A1c in children and adolescents with poorly controlled type 1 diabetes.
Jackson, A., Ternand, C., Brunzell, C., Kleinschmidt, T., Dew, D., & Moran, A. (2003). Insulin glargine improves hemoglobin A1c in children and adolescents with poorly controlled type 1 diabetes. Pediatric diabetes, 4(2), 64-69.

Abnormal glucose tolerance in cystic fibrosis: Why should patients be screened?
Moran, A., & Milla, C. (2003). Abnormal glucose tolerance in cystic fibrosis: Why should patients be screened?. JOURNAL OF PEDIATRICS, 142(2), 97-99.

Continuous propofol infusion in 142 critically ill children
Cornfield, D. N., Tegtmeyer, K., Nelson, M. D., Milla, C. E., & Sweeney, M. (2002). Continuous propofol infusion in 142 critically ill children. PEDIATRICS, 110(6), 1177-1181.

Surfactant protein A decreases lung injury and mortality after murine marrow transplantation
Yang, S. X., Milla, C., Panoskaltsis-Mortari, A., Hawgood, S., Blazar, B. R., & Haddad, I. Y. (2002). Surfactant protein A decreases lung injury and mortality after murine marrow transplantation. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 27(3), 297-305.

Abnormal lipid concentrations in cystic fibrosis
FIGUEROA, V., Milla, C., Parks, E. J., Schwarzenberg, S. J., & Moran, A. (2002). Abnormal lipid concentrations in cystic fibrosis. AMERICAN JOURNAL OF CLINICAL NUTRITION, 75(6), 1005-1011.

Effects of oxidant stress on inflammation and survival of iNOS knockout mice after marrow transplantation
Yang, S. X., Porter, V. A., Cornfield, D. N., Milla, C., Panoskaltsis-Mortari, A., & Haddad, I. Y. (2001). Effects of oxidant stress on inflammation and survival of iNOS knockout mice after marrow transplantation. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 281(4), L922-L930.

Insulin and glucose excursion following premeal insulin lispro or repaglinide in cystic fibrosis-related diabetes
Moran, A., Phillips, J., & Milla, C. (2001). Insulin and glucose excursion following premeal insulin lispro or repaglinide in cystic fibrosis-related diabetes. DIABETES CARE, 24(10), 1706-1710.

Protein metabolism in clinically stable adult cystic fibrosis patients with abnormal glucose tolerance
Moran, A., Milla, C., Ducret, R., & Nair, K. S. (2001). Protein metabolism in clinically stable adult cystic fibrosis patients with abnormal glucose tolerance. DIABETES, 50(6), 1336-1343.

Human surfactant protein A suppresses T cell-dependent inflammation and attenuates the manifestations of idiopathic pneumonia syndrome in mice
Yang, S. X., Milla, C., Panoskaltsis-Mortari, A., Ingbar, D. H., Blazar, B. R., & Haddad, I. Y. (2001). Human surfactant protein A suppresses T cell-dependent inflammation and attenuates the manifestations of idiopathic pneumonia syndrome in mice. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 24(5), 527-536.

Trends in pulmonary function in patients with cystic fibrosis correlate with the degree of glucose intolerance at baseline
Milla, C. E., Warwick, W. J., & Moran, A. (2000). Trends in pulmonary function in patients with cystic fibrosis correlate with the degree of glucose intolerance at baseline. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 162(3), 891-895.

Randomized, controlled trial of low-dose inhaled nitric oxide in the treatment of term and near-term infants with respiratory failure and pulmonary hypertension
Cornfield, D. N., Maynard, R. C., deRegnier, R. Ao., Guiang, S. F., Barbato, J. E., & Milla, C. E. (1999). Randomized, controlled trial of low-dose inhaled nitric oxide in the treatment of term and near-term infants with respiratory failure and pulmonary hypertension. PEDIATRICS, 104(5), 1089-1094.

Recombinant human DNase in cystic fibrosis
Milla, C. E. (1999). Recombinant human DNase in cystic fibrosis. LANCET, 354(9176), 428-428.

NO causes perinatal pulmonary vasodilation through K+-channel activation and intracellular Ca2+ release
Saqueton, C. B., Miller, R. B., Porter, V. A., Milla, C. E., & Cornfield, D. N. (1999). NO causes perinatal pulmonary vasodilation through K+-channel activation and intracellular Ca2+ release. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 276(6), L925-L932.

High levels of peroxynitrite are generated in the lungs of irradiated mice given cyclophosphamide and allogeneic T cells - A potential mechanism of injury after marrow transplantation
Haddad, I. Y., Panoskaltsis-Mortari, A., Ingbar, D. H., Yang, S. X., Milla, C. E., & Blazar, B. R. (1999). High levels of peroxynitrite are generated in the lungs of irradiated mice given cyclophosphamide and allogeneic T cells - A potential mechanism of injury after marrow transplantation. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 20(6), 1125-1135.

Allergic bronchopulmonary aspergillosis and cystic fibrosis
Milla, C. E. (1999). Allergic bronchopulmonary aspergillosis and cystic fibrosis. PEDIATRIC PULMONOLOGY, 27(2), 71-73.

Long term effects of aerosolised rhDNase on pulmonary disease progression in patients with cystic fibrosis
Milla, C. E. (1998). Long term effects of aerosolised rhDNase on pulmonary disease progression in patients with cystic fibrosis. THORAX, 53(12), 1014-1017.

Effects of inhaled nitric oxide and oxygen in high-altitude pulmonary edema
Anand, I. S., Prasad, B. Ak., Chugh, S. S., Rao, K. Rm., Cornfield, D. N., & Selvamurthy, W. (1998). Effects of inhaled nitric oxide and oxygen in high-altitude pulmonary edema. CIRCULATION, 98(22), 2441-2445.

Risk of death in cystic fibrosis patients with severely compromised lung function
Milla, C. E., & Warwick, W. J. (1998). Risk of death in cystic fibrosis patients with severely compromised lung function. CHEST, 113(5), 1230-1234.

PCR ribotyping and endonuclease subtyping in the epidemiology of Burkholderia cepacio infection
Shreve, M. R., Johnson, S. J., Milla, C. E., Wielinski, C. L., & Regelmann, W. E. (1997). PCR ribotyping and endonuclease subtyping in the epidemiology of Burkholderia cepacio infection. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 155(3), 984-989.

Glycemic response to dietary supplements in cystic fibrosis is dependent on the carbohydrate content of the formula
Milla, C., Doherty, L., Raatz, S., Schwarzenberg, S. J., Regelmann, W., & Moran, A. (1996). Glycemic response to dietary supplements in cystic fibrosis is dependent on the carbohydrate content of the formula. JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 20(3), 182-186.

Clinical significance of the recovery of Aspergillus species from the respiratory secretions of cystic fibrosis patients
Milla, C. E., Wielinski, C. L., & Regelmann, W. E. (1996). Clinical significance of the recovery of Aspergillus species from the respiratory secretions of cystic fibrosis patients. PEDIATRIC PULMONOLOGY, 21(1), 6-10.

HIGH-STRENGTH PANCREATIC-ENZYMES
Milla, C. E., Wielinski, C. L., & Warwick, W. J. (1994). HIGH-STRENGTH PANCREATIC-ENZYMES. LANCET, 343(8897), 599-599.