Publications by authors named "Carlos Milla"

100Publications

Defining the Clinical Utility of the Lung Clearance Index: Are We There Yet?

Am J Respir Crit Care Med 2020 Nov 12. Epub 2020 Nov 12.

Stanford University, Center for Excellence in Pulmonary Biology, Palo Alto, California, United States;

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November 2020

An autonomous wearable system for diurnal sweat biomarker data acquisition.

Lab Chip 2020 12;20(24):4582-4591

Interconnected and Integrated Bioelectronics Lab (I2BL), Henry Samueli School of Engineering and Applied Science, University of California, Los Angeles, CA, USA. and Department of Electrical and Computer Engineering, University of California, Los Angeles, CA, USA and Department of Bioengineering, University of California, Los Angeles, CA, USA.

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December 2020

Area under the curve achievement of once daily tobramycin in children with cystic fibrosis during clinical care.

Pediatr Pulmonol 2020 12 3;55(12):3343-3350. Epub 2020 Sep 3.

Department of Pediatrics, Stanford University, Stanford, California.

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December 2020

Noninvasive wearable electroactive pharmaceutical monitoring for personalized therapeutics.

Proc Natl Acad Sci U S A 2020 08 27;117(32):19017-19025. Epub 2020 Jul 27.

Interconnected & Integrated Bioelectronics Lab (IBL), Department of Electrical and Computer Engineering, University of California, Los Angeles, CA 90095;

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August 2020

Methods for Extraction and Detection of Pf Bacteriophage DNA from the Sputum of Patients with Cystic Fibrosis.

Phage (New Rochelle) 2020 06 16;1(2):100-108. Epub 2020 Jun 16.

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University, Stanford, California, USA.

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June 2020

Natural Perspiration Sampling and in Situ Electrochemical Analysis with Hydrogel Micropatches for User-Identifiable and Wireless Chemo/Biosensing.

ACS Sens 2020 01 1;5(1):93-102. Epub 2019 Dec 1.

The Stanford Cystic Fibrosis Center, Center for Excellence in Pulmonary Biology , Stanford School of Medicine , Palo Alto , California 94305 , United States.

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January 2020

Proof of concept for identifying cystic fibrosis from perspiration samples.

Proc Natl Acad Sci U S A 2019 12 18;116(49):24408-24412. Epub 2019 Nov 18.

Department of Chemistry, Stanford University, Stanford, CA 94305;

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December 2019

New Algorithm for the Integration of Ultrasound Into Cystic Fibrosis Liver Disease Screening.

J Pediatr Gastroenterol Nutr 2019 10;69(4):404-410

Division of Pediatric Pulmonary Medicine, Stanford University, Palo Alto, CA.

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October 2019

Salivary Thiocyanate as a Biomarker of Cystic Fibrosis Transmembrane Regulator Function.

Anal Chem 2019 06 4;91(12):7929-7934. Epub 2019 Jun 4.

Center for Excellence in Pulmonary Biology, Department of Pediatrics , Stanford University , Stanford , California 94304 , United States.

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June 2019

Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults.

Sci Rep 2018 11 2;8(1):16233. Epub 2018 Nov 2.

Cystic Fibrosis Research Laboratory, Stanford University, Stanford, CA, 94305, USA.

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November 2018

Tear Down This Wall: Diversity and Disparities in Cystic Fibrosis.

Am J Respir Crit Care Med 2018 10;198(8):983-984

1 Center for Excellence in Pulmonary Biology Stanford University School of Medicine Stanford, California.

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October 2018

Age-related heterogeneity in dental caries and associated risk factors in individuals with cystic fibrosis ages 6-20 years: A pilot study.

J Cyst Fibros 2018 11 10;17(6):747-759. Epub 2018 Jul 10.

University of Missouri - Kansas City, School of Dentistry, Department of Dental Public, Health and Behavioral Science, 650 E. 25th St., Kansas City, MO 64108, USA.

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November 2018

KB001-A, a novel anti-inflammatory, found to be safe and well-tolerated in cystic fibrosis patients infected with Pseudomonas aeruginosa.

J Cyst Fibros 2018 07 29;17(4):484-491. Epub 2017 Dec 29.

University Hospitals Rainbow Babies and Children's Hospital, Cleveland, OH 44106, USA; Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

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July 2018

Ivacaftor restores CFTR-dependent sweat gland fluid secretion in cystic fibrosis subjects with S945L alleles.

J Cyst Fibros 2018 03 24;17(2):179-185. Epub 2017 Dec 24.

Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA. Electronic address:

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March 2018

Implementation of Depression Screening and Global Health Assessment in Pediatric Subspecialty Clinics.

J Adolesc Health 2017 Nov 19;61(5):591-598. Epub 2017 Aug 19.

Division of Endocrinology and Diabetes, Department of Pediatrics, Stanford University School of Medicine, Stanford, California; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California. Electronic address:

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November 2017

Lung clearance index is sensitive to small airway disease in pediatric lung transplant recipients.

J Heart Lung Transplant 2017 Sep 10;36(9):980-984. Epub 2017 May 10.

Stanford University, Palo Alto, California; Center for Excellence in Pulmonary Biology Department of Pediatrics, Stanford University School of Medicine, Palo Alto, California. Electronic address:

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September 2017

The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements.

PLoS One 2017 18;12(4):e0175486. Epub 2017 Apr 18.

Cystic Fibrosis Research Laboratory, Stanford University, Stanford, California, United States of America.

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May 2017

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis.

J Pediatr 2017 02;181S:S45-S51.e1

Department for Women's and Children's Health, University of Liverpool, Institute in the Park, Alder Hey Children's Hospital, Liverpool, United Kingdom.

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February 2017

Lumacaftor/Ivacaftor in Patients Aged 6-11 Years with Cystic Fibrosis and Homozygous for F508del-CFTR.

Am J Respir Crit Care Med 2017 04;195(7):912-920

4 Pulmonary and Sleep Medicine, Seattle Children's Hospital, Seattle, Washington; and.

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April 2017

Evaporimeter and Bubble-Imaging Measures of Sweat Gland Secretion Rates.

PLoS One 2016 21;11(10):e0165254. Epub 2016 Oct 21.

Cystic Fibrosis Research Laboratory, Stanford University, Stanford, California, United States of America.

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June 2017

Response.

Chest 2016 09;150(3):753

Department of Pediatrics, Division of General Pediatrics, Center for Policy, Outcomes and Prevention, Stanford University School of Medicine, Stanford, CA.

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September 2016

Airway epithelial homeostasis and planar cell polarity signaling depend on multiciliated cell differentiation.

JCI Insight 2016 Aug;1(13)

Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.

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August 2016

Sweat chloride testing: controversies and issues.

Lancet Respir Med 2016 08;4(8):605-607

Department of Pediatrics, Stanford University, Stanford, CA, USA; Department of Psychology, Stanford University, Stanford, CA, USA.

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August 2016

The evolving spectrum of ciliopathies and respiratory disease.

Authors:
Carlos E Milla

Curr Opin Pediatr 2016 06;28(3):339-47

The Stanford Cystic Fibrosis Center, Stanford, California, USA.

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June 2016

Assessing Differences in Mortality Rates and Risk Factors Between Hispanic and Non-Hispanic Patients With Cystic Fibrosis in California.

Chest 2016 Feb 12;149(2):380-389. Epub 2016 Jan 12.

Department of Pediatrics, Division of General Pediatrics, Center for Policy, Outcomes and Prevention, Stanford University School of Medicine, Stanford, CA.

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February 2016

Pulmonary nocardiosis in an immunocompetent patient with cystic fibrosis.

Case Rep Pulmonol 2015 15;2015:984171. Epub 2015 Apr 15.

Division of Pulmonary Medicine, Department of Pediatrics, Stanford Children's Hospital, 725 Welch Road, Palo Alto, CA 94304, USA.

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May 2015

Inhaled β2-Agonist Therapy Increases Functional Residual Capacity in Mechanically Ventilated Children With Respiratory Failure.

Pediatr Crit Care Med 2015 Sep;16(7):e189-93

1Division of Pediatric Critical Care Medicine, Sheikh Khalifa Medical City (SKMC) in affiliation with Cleveland Clinic, Abu Dhabi, United Arab Emirates. 2Respiratory Therapy Department, Lucile Packard Children's Hospital at Stanford University, Palo Alto, CA. 3Division of Pulmonary Medicine, Center for Excellence in Pulmonary Biology, Stanford University School of Medicine, Stanford, CA. 4Department of Pediatrics, Center for Excellence in Pulmonary Biology, Stanford University School of Medicine, Stanford, CA.

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September 2015

Recent advances in cystic fibrosis.

Curr Opin Pediatr 2015 Jun;27(3):317-24

aThe Stanford Cystic Fibrosis Center, Palo Alto bCenter for Excellence in Pulmonary Biology, Stanford University School of Medicine, Stanford, California, USA.

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June 2015

A little CFTR goes a long way: CFTR-dependent sweat secretion from G551D and R117H-5T cystic fibrosis subjects taking ivacaftor.

PLoS One 2014 10;9(2):e88564. Epub 2014 Feb 10.

Cystic Fibrosis Research Laboratory, Stanford University, Stanford, California, United States of America ; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America ; Department of Psychology, Stanford University, Stanford, California, United States of America.

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October 2014

Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial.

Lancet Respir Med 2013 Oct 10;1(8):630-638. Epub 2013 Sep 10.

Division of Respiratory Medicine, Department of Paediatrics, Physiology and Experimental Medicine, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.

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October 2013

In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands.

PLoS One 2013 24;8(10):e77114. Epub 2013 Oct 24.

Cystic Fibrosis Research Laboratory, Stanford University, Stanford, California, United States of America ; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America ; Department of Psychology, Stanford University, Stanford, California, United States of America.

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August 2014

Pricing for orphan drugs: will the market bear what society cannot?

JAMA 2013 Oct;310(13):1343-4

Department of Pediatrics, University of Massachusetts Medical School, Worcester, MA 01655, USA.

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October 2013

Anti-PcrV antibody in cystic fibrosis: a novel approach targeting Pseudomonas aeruginosa airway infection.

Pediatr Pulmonol 2014 Jul 9;49(7):650-8. Epub 2013 Sep 9.

Center for Excellence in Pulmonary Biology, Stanford University, 770 Welch Road, Suite 350, Palo Alto, CA 94304.

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July 2014

Cystic fibrosis in the era of genomic medicine.

Authors:
Carlos E Milla

Curr Opin Pediatr 2013 Jun;25(3):323-8

Department of Pediatrics, Center for Excellence in Pulmonary Biology, Stanford University, 770 Welch Road, Suite 350, Palo Alto, CA 94304, USA.

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June 2013

Quantitative analysis of the human airway microbial ecology reveals a pervasive signature for cystic fibrosis.

Sci Transl Med 2012 Sep;4(153):153ra130

Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.

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September 2012

Effect of endoscopic sinus surgery on pulmonary status of adults with cystic fibrosis.

Otolaryngol Head Neck Surg 2012 Sep 18;147(3):557-62. Epub 2012 Apr 18.

The Minnesota CF Center, Department of Medicine, University of Minnesota School of Medicine, Minneapolis, Minnesota 55455, USA.

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September 2012

Dyspnea in a patient with Raynaud's phenomenon: the uncovering of interstitial lung disease.

Pediatr Pulmonol 2012 Sep 29;47(9):926-7. Epub 2012 Mar 29.

Stanford University, Pediatric Pulmonary Division, Palo Alto, CA 94040, USA.

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September 2012

Pulmonary complications of endocrine and metabolic disorders.

Paediatr Respir Rev 2012 Mar 22;13(1):23-8. Epub 2011 Feb 22.

Center for Excellence in Pulmonary Biology, Stanford University Medical School, Palo Alto, CA, USA.

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March 2012

CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR.

J Med Genet 2011 Apr 20;48(4):235-41. Epub 2010 Nov 20.

McKusick-Nathans Institute of Genetic Medicine, 733 North Broadway, Johns Hopkins Medical Institutions, Baltimore, MD 21205, USA.

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April 2011

Characteristics of gastroesophageal reflux in adults with cystic fibrosis.

J Cyst Fibros 2010 Sep 31;9(5):365-70. Epub 2010 Jul 31.

Department of Pediatrics, Stanford University School of Medicine, 725 Welch Road, Stanford CA 94305, United States.

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September 2010

Comparison of settings used for high-frequency chest-wall compression in cystic fibrosis.

Respir Care 2010 Jun;55(6):695-701

Department of Medicine, Hennepin County Medical Center, University of Minnesota School of Medicine, Mail Stop G-5, 701 Park Avenue, Minneapolis, MN 55415, USA.

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June 2010

Nutrition in cystic fibrosis.

Semin Respir Crit Care Med 2009 Oct 16;30(5):579-86. Epub 2009 Sep 16.

The Stanford Cystic Fibrosis Center, Center for Excellence in Pulmonary Biology, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, California 94304, USA.

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October 2009

Cystic fibrosis related diabetes.

Paediatr Respir Rev 2009 Sep 14;10(3):118-23; quiz 123. Epub 2009 Jul 14.

Centre for Excellence in Pulmonary Biology, Stanford Cystic Fibrosis Centre, Stanford University Medical School, Palo Alto, CA, USA.

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September 2009

Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis.

Pediatr Pulmonol 2009 Apr;44(4):330-9

Miller Children's Hospital at Long Beach Memorial Medical Center, Long Beach, California 90806, USA.

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April 2009

Associations of psychosocial factors with health outcomes among youth with cystic fibrosis.

Pediatr Pulmonol 2009 Jan;44(1):46-53

Division of Epidemiology & Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota, MN 55454, USA.

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January 2009

Steroid-sparing effect of omalizumab for allergic bronchopulmonary aspergillosis and cystic fibrosis.

Pediatr Pulmonol 2008 Jun;43(6):607-10

The Minnesota CF Center, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota, USA.

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June 2008

Comparison of high-frequency chest wall oscillation with differing waveforms for airway clearance in cystic fibrosis.

Chest 2007 Oct 21;132(4):1227-32. Epub 2007 Sep 21.

Minnesota Cystic Fibrosis Center, Department of Medicine, University of Minnesota School of Medicine, Minneapolis, MN, USA.

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October 2007

Gender differences in treatment adherence among youth with cystic fibrosis: development of a new questionnaire.

J Cyst Fibros 2008 Mar 24;7(2):154-64. Epub 2007 Aug 24.

Division of Epidemiology & Community Health, University of Minnesota, School of Public Health, 1300 South 2nd Street, Suite 300, Minneapolis, MN 55454, United States.

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March 2008

Nutrition and lung disease in cystic fibrosis.

Authors:
Carlos E Milla

Clin Chest Med 2007 Jun;28(2):319-30

Department of Pediatrics, Center for Excellence in Pulmonary Biology, Stanford University, 770 Welch Road, Palo Alto, CA 94304, USA.

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June 2007

Hepatolithiasis and cholangiocarcinoma in cystic fibrosis: a case series and review of the literature.

Dig Dis Sci 2007 Oct 19;52(10):2638-42. Epub 2007 Apr 19.

Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.

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October 2007

Microvascular complications in cystic fibrosis-related diabetes.

Diabetes Care 2007 May 23;30(5):1056-61. Epub 2007 Feb 23.

Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55454, USA.

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May 2007

Different frequencies should be prescribed for different high frequency chest compression machines.

Biomed Instrum Technol 2006 Jul-Aug;40(4):319-24

University of Minnesota Cystic Fibrosis Center, Minneapolis, MN, USA.

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January 2007

Cystic fibrosis pulmonary exacerbations.

J Pediatr 2006 Feb;148(2):259-64

Department of Pediatrics, Cell Biology and Physiology, Washington University School of Medicine, St. Louis Children's Hospital, 660 South Euclid Avenue, St. Louis, MO 63110, USA.

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February 2006

Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis.

Diabetes Care 2005 Sep;28(9):2141-4

Department of Pediatrics, MMC 742, Minnesota Cystic Fibrosis Center, University of Minnesota, 420 Delaware St. WE, Minneapolis, Minnesota 55455, USA.

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September 2005

Absence of host tumor necrosis factor receptor 1 attenuates manifestations of idiopathic pneumonia syndrome.

Am J Physiol Lung Cell Mol Physiol 2005 May 17;288(5):L942-9. Epub 2004 Dec 17.

Dept. of Pediatrics, University of Minnesota, Minneapolis, MN 55455, USA.

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May 2005

Altered airway responsiveness in CD38-deficient mice.

Am J Respir Cell Mol Biol 2005 Feb 19;32(2):149-56. Epub 2004 Nov 19.

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, 1971 Commonwealth Avenue, Saint Paul, MN 55108, USA.

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February 2005

Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance.

Metabolism 2004 Nov;53(11):1467-72

Division of Endocrinology, Department of Pediatrics, University of Minnesota, MN 55455, USA.

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November 2004

Association of nutritional status and pulmonary function in children with cystic fibrosis.

Authors:
Carlos E Milla

Curr Opin Pulm Med 2004 Nov;10(6):505-9

The Minnesota CF Center, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.

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November 2004

Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis.

J Lab Clin Med 2004 Sep;144(3):127-33

Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN 55455, USA.

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September 2004

High-frequency chest compression: effect of the third generation compression waveform.

Biomed Instrum Technol 2004 Jul-Aug;38(4):322-8

Cystic Fibrosis Center, University of Minnesota Medical School, Minneapolis, MN 55455, USA.

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November 2004

Myeloperoxidase deficiency enhances inflammation after allogeneic marrow transplantation.

Am J Physiol Lung Cell Mol Physiol 2004 Oct 12;287(4):L706-14. Epub 2004 Mar 12.

Division of Pulmonary and Critical Care, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455, USA.

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October 2004

Longitudinal changes in growth parameters are correlated with changes in pulmonary function in children with cystic fibrosis.

Pediatrics 2003 Sep;112(3 Pt 1):588-92

Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis, USA.

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September 2003