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105 results for Ranganathan,+Sarath+C.

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ArticlesPeer ReviewedFull Text
Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children
Author / Creator:Muhlebach, Marianne S. ; Zorn, Bryan T. ; Esther, Charles R. ; Hatch, Joseph E. ; Murray, Conor P. ; Turkovic, Lidija ; Ranganathan, Sarath C. ; Boucher, Richard C. ; Stick, Stephen M. ; Wolfgang, Matthew C.
Publisher:United States: Public Library of Science
Journal title:PLoS pathogens, 2018-01, Vol.14 (1), p.e1006798-e1006798
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A Three-Way Comparison of Tuberculin Skin Testing, QuantiFERON-TB Gold and T-SPOT.TB in Children
Author / Creator:Connell, Tom G. ; Ritz, Nicole ; Paxton, Georgia A. ; Buttery, Jim P. ; Curtis, Nigel ; Ranganathan, Sarath C.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2008-07, Vol.3 (7), p.e2624-e2624
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Telehealth spirometry for children with cystic fibrosis
Author / Creator:Logie, Karla ; Welsh, Liam ; Ranganathan, Sarath C
Publisher:England
Journal title:Archives of disease in childhood, 2020-12, Vol.105 (12), p.1203-1205
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Bile Acid Signal Molecules Associate Temporally with Respiratory Inflammation and Microbiome Signatures in Clinically Stable Cystic Fibrosis Patients
Author / Creator:Flynn, Stephanie ; Reen, F. Jerry ; Caparrós-Martín, Jose A. ; Woods, David F. ; Peplies, Jörg ; Ranganathan, Sarath C. ; Stick, Stephen M. ; O'Gara, Fergal
Publisher:MDPI
Journal title:Microorganisms (Basel), 2020-11, Vol.8 (11), p.1741
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The Detection of Bile Acids in the Lungs of Paediatric Cystic Fibrosis Patients Is Associated with Altered Inflammatory Patterns
Author / Creator:Caparrós-Martín, Jose A. ; Flynn, Stephanie ; Reen, F. Jerry ; Woods, David F. ; Agudelo-Romero, Patricia ; Ranganathan, Sarath C. ; Stick, Stephen M. ; O’Gara, Fergal
Publisher:Switzerland: MDPI AG
Journal title:Diagnostics (Basel), 2020-05, Vol.10 (5), p.282
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DNA methylation biomarkers of future health outcomes in children
Author / Creator:Shanthikumar, Shivanthan ; Neeland, Melanie R. ; Maksimovic, Jovana ; Ranganathan, Sarath C. ; Saffery, Richard
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Molecular and cellular pediatrics, 2020-07, Vol.7 (1), Article 7
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The Evolution of Airway Function in Early Childhood Following Clinical Diagnosis of Cystic Fibrosis
Author / Creator:Ranganathan, Sarath C ; Stocks, Janet ; Dezateux, Carol ; Bush, Andrew ; Wade, Angie ; Carr, Siobhan ; Castle, Rosemary ; Dinwiddie, Robert ; Hoo, Ah-Fong ; Lum, Sooky ; Price, John ; Stroobant, John ; Wallis, Colin
Publisher:New York, NY: Am Thoracic Soc
Journal title:American journal of respiratory and critical care medicine, 2004-04, Vol.169 (8), p.928-933
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Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?
Author / Creator:Ranganathan, Sarath C. ; Hall, Graham L. ; Sly, Peter D. ; Stick, Stephen M. ; Douglas, Tonia A.
Publisher:United States: American Thoracic Society
Journal title:American journal of respiratory and critical care medicine, 2017-06, Vol.195 (12), p.1567-1575
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PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis
Author / Creator:Rosenow, Tim ; Oudraad, Merel C. J. ; Murray, Conor P. ; Turkovic, Lidija ; Kuo, Wieying ; de Bruijne, Marleen ; Ranganathan, Sarath C. ; Tiddens, Harm A. W. M. ; Stick, Stephen M.
Publisher:United States: American Thoracic Society
Journal title:American journal of respiratory and critical care medicine, 2015-05, Vol.191 (10), p.1158-1165
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Lung Clearance Index and Structural Lung Disease on Computed Tomography in Early Cystic Fibrosis
Author / Creator:Ramsey, Kathryn A. ; Rosenow, Tim ; Turkovic, Lidija ; Skoric, Billy ; Banton, Georgia ; Adams, Anne-Marie ; Simpson, Shannon J. ; Murray, Conor ; Ranganathan, Sarath C. ; Stick, Stephen M. ; Hall, Graham L.
Publisher:United States: American Thoracic Society
Journal title:American journal of respiratory and critical care medicine, 2016-01, Vol.193 (1), p.60-67
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The lower airway microbiota in early cystic fibrosis lung disease: a longitudinal analysis
Author / Creator:Frayman, Katherine B ; Armstrong, David S ; Carzino, Rosemary ; Ferkol, Thomas W ; Grimwood, Keith ; Storch, Gregory A ; Teo, Shu Mei ; Wylie, Kristine M ; Ranganathan, Sarath C
Publisher:England: BMJ Publishing Group LTD
Journal title:Thorax, 2017-12, Vol.72 (12), p.1104-1112
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Progression of early structural lung disease in young children with cystic fibrosis assessed using CT
Author / Creator:Mott, Lauren S ; Park, Judy ; Murray, Conor P ; Gangell, Catherine L ; de Klerk, Nicholas H ; Robinson, Philip J ; Robertson, Colin F ; Ranganathan, Sarath C ; Sly, Peter D ; Stick, Stephen M
Publisher:London: BMJ Publishing Group
Journal title:Thorax, 2012-06, Vol.67 (6), p.509-516
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Antibiotic Management of Lung Infections in Cystic Fibrosis. I. The Microbiome, Methicillin-Resistant Staphylococcus aureus , Gram-Negative Bacteria, and Multiple Infections
Author / Creator:Chmiel, James F. ; Aksamit, Timothy R. ; Chotirmall, Sanjay H. ; Dasenbrook, Elliott C. ; Elborn, J. Stuart ; LiPuma, John J. ; Ranganathan, Sarath C. ; Waters, Valerie J. ; Ratjen, Felix A.
Publisher:United States: American Thoracic Society
Journal title:Annals of the American Thoracic Society, 2014-09, Vol.11 (7), p.1120-1129
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Lung Disease at Diagnosis in Infants with Cystic Fibrosis Detected by Newborn Screening
Author / Creator:Sly, Peter D ; Brennan, Siobhain ; Gangell, Catherine ; de Klerk, Nicholas ; Murray, Conor ; Mott, Lauren ; Stick, Stephen M ; Robinson, Philip J ; Robertson, Colin F ; Ranganathan, Sarath C ; on behalf of Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST-CF)
Publisher:New York, NY: Am Thoracic Soc
Journal title:American journal of respiratory and critical care medicine, 2009-07, Vol.180 (2), p.146-152
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ArticlesPeer ReviewedFull Text
Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis
Author / Creator:Ranganathan, Sarath C ; Parsons, Faith ; Gangell, Catherine ; Brennan, Siobhan ; Stick, Stephen M ; Sly, Peter D
Publisher:England: BMJ Publishing Group Ltd and British Thoracic Society
Journal title:Thorax, 2011-05, Vol.66 (5), p.408-413
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ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death
Author / Creator:Ogier, Jacqueline M. ; Gao, Yujing ; Dunne, Eileen M. ; Wilson, Michael A. ; Ranganathan, Sarath C. ; Tesch, Gregory H. ; Nikolic Paterson, David J. ; Dabdoub, Alain ; Burt, Rachel A. ; Nayagam, Bryony A. ; Lockhart, Paul J.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of molecular medicine (Berlin, Germany), 2022-05, Vol.100 (5), p.797-813
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Antibiotic Management of Lung Infections in Cystic Fibrosis. II. Nontuberculous Mycobacteria, Anaerobic Bacteria, and Fungi
Author / Creator:Chmiel, James F. ; Aksamit, Timothy R. ; Chotirmall, Sanjay H. ; Dasenbrook, Elliott C. ; Elborn, J. Stuart ; LiPuma, John J. ; Ranganathan, Sarath C. ; Waters, Valerie J. ; Ratjen, Felix A.
Publisher:United States: American Thoracic Society
Journal title:Annals of the American Thoracic Society, 2014-10, Vol.11 (8), p.1298-1306
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The implementation of a cystic fibrosis annual review process in a tertiary paediatric hospital
Author / Creator:Armiento, Raffaela ; Ranganathan, Sarath C ; Harrison, Joanne
Publisher:England: BMJ Publishing Group LTD
Journal title:Archives of disease in childhood. Education and practice edition, 2018-10, Vol.103 (5), p.241-243
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Multiple-Breath Washout Outcomes Are Sensitive to Inflammation and Infection in Children with Cystic Fibrosis
Author / Creator:Ramsey, Kathryn A. ; Foong, Rachel E. ; Grdosic, Jasmine ; Harper, Alana ; Skoric, Billy ; Clem, Charles ; Davis, Miriam ; Turkovic, Lidija ; Stick, Stephen M. ; Davis, Stephanie D. ; Ranganathan, Sarath C. ; Hall, Graham L.
Publisher:United States: American Thoracic Society
Journal title:Annals of the American Thoracic Society, 2017-09, Vol.14 (9), p.1436-1442
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Correction to: ASK1 is a novel molecular target for preventing aminoglycoside‑induced hair cell death
Author / Creator:Ogier, Jacqueline M. ; Gao, Yujing ; Dunne, Eileen M. ; Wilson, Michael A. ; Ranganathan, Sarath C. ; Tesch, Gregory H. ; Nikolic Paterson, David J. ; Dabdoub, Alain ; Burt, Rachel A. ; Nayagam, Bryony A. ; Lockhart, Paul J.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of molecular medicine (Berlin, Germany), 2022-05, Vol.100 (5), p.815-815
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Showing 1 to 20 of 105 results

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Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children

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A Three-Way Comparison of Tuberculin Skin Testing, QuantiFERON-TB Gold and T-SPOT.TB in Children

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Telehealth spirometry for children with cystic fibrosis

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Bile Acid Signal Molecules Associate Temporally with Respiratory Inflammation and Microbiome Signatures in Clinically Stable Cystic Fibrosis Patients

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The Detection of Bile Acids in the Lungs of Paediatric Cystic Fibrosis Patients Is Associated with Altered Inflammatory Patterns

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DNA methylation biomarkers of future health outcomes in children

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The Evolution of Airway Function in Early Childhood Following Clinical Diagnosis of Cystic Fibrosis

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Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?

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PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis

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Lung Clearance Index and Structural Lung Disease on Computed Tomography in Early Cystic Fibrosis

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The lower airway microbiota in early cystic fibrosis lung disease: a longitudinal analysis

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Progression of early structural lung disease in young children with cystic fibrosis assessed using CT

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Antibiotic Management of Lung Infections in Cystic Fibrosis. I. The Microbiome, Methicillin-Resistant Staphylococcus aureus , Gram-Negative Bacteria, and Multiple Infections

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Lung Disease at Diagnosis in Infants with Cystic Fibrosis Detected by Newborn Screening

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Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis

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ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death

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Antibiotic Management of Lung Infections in Cystic Fibrosis. II. Nontuberculous Mycobacteria, Anaerobic Bacteria, and Fungi

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The implementation of a cystic fibrosis annual review process in a tertiary paediatric hospital

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Multiple-Breath Washout Outcomes Are Sensitive to Inflammation and Infection in Children with Cystic Fibrosis

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Correction to: ASK1 is a novel molecular target for preventing aminoglycoside‑induced hair cell death

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