Publications

To date there have been 133 publications from AREST CF research:

 

2015

Douglas T, Jordan B, Priddis L, Anderson V, Sheehan J, Kane RT, et al. Protocol for a study of the psychosocial determinants of health in early childhood among children with cystic fibrosis. J Adv Nurs. 2015.

 

Schultz A, Stick S. Early pulmonary inflammation and lung damage in children with cystic fibrosis. Respirology. 2015;20(4):569-78.

 

Rosenow T, Oudraad MC, Murray CP, Turkovic L, Kuo W, de Bruijne M, Ranganathan SC, Tiddens HA, Stick SM; AREST CF. PRAGMA-CF: a Quantitative Structural Lung Disease CT Outcome in Young Children with Cystic Fibrosis. Am J Respir Crit Care Med.

 

2014

Ramsey KA, Ranganathan S, Park J, et al. Early respiratory infection is associated with reduced spirometry in children with cystic fibrosis. American journal of respiratory and critical care medicine 2014;190:1111-6.

 

Kettle AJ, Turner R, Gangell CL, et al. Oxidation contributes to low glutathione in the airways of children with cystic fibrosis. The European respiratory journal 2014;44:122-9.

 

Garratt LW, Sutanto EN, Foo CJ, et al. Determinants of culture success in an airway epithelium sampling program of young children with cystic fibrosis. Experimental lung research 2014;40:447-59.

 

Fantino E, Gangell CL, Hartl D, Sly PD, Arest CF. Airway, but not serum or urinary, levels of YKL-40 reflect inflammation in early cystic fibrosis lung disease. BMC pulmonary medicine 2014;14(6):28.

 

Gangell CL, Shackleton C, Poreddy S, Kappers J, Gaydon JE, Sloots TP, Stick SM, Ranganathan SC, Sly PD. Feasibility of parental collected nasal swabs for virus detection in young children with cystic fibrosis. Journal of Cystic Fibrosis 2014;13:661-66.

 

Taccetti G, Sly PD.  Early detection of infection with Pseudomonas aeruginosa in cystic fibrosis: The Holy Grail or an achievable goal? J Cyst Fibros. 2014;13:491-493.

 

Zemanick ET, Wagner BD, Robertson CE, et al. Assessment of Airway Microbiota and Inflammation in Cystic Fibrosis Using Multiple Sampling Methods. Annals of the American Thoracic Society 2015;12(2):221-29.

 

Welsh L, Robertson CF, Ranganathan SC. Increased rate of lung function decline in Australian adolescents with cystic fibrosis. Pediatric pulmonology 2014;49:873-7.

 

Welsh L, Nesci C, Tran H, Tomai M, Ranganathan S. Lung clearance index during hospital admission in school-age children with cystic fibrosis. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2014;13:687-91.

 

Tiddens HA, Stick SM, Davis S. Multi-modality monitoring of cystic fibrosis lung disease: the role of chest computed tomography. Paediatric respiratory reviews 2014;15:92-7.

 

Sheehan J, Hiscock H, Massie J, Jaffe A, Hay M. Caregiver coping, mental health and child problem behaviours in cystic fibrosis: a cross-sectional study. International journal of behavioral medicine 2014;21:211-20.

 

Ramsey KA, Ranganathan S. Interpretation of lung function in infants and young children with cystic fibrosis. Respirology 2014;19:792-9.

 

Massie J, Ioannou L, Delatycki M. Prenatal and preconception population carrier screening for cystic fibrosis in Australia: where are we up to? The Australian & New Zealand journal of obstetrics & gynaecology 2014;54:503-9.

 

Massie J, Gillam L. Uncertain diagnosis after newborn screening for cystic fibrosis: An ethics-based approach to a clinical dilemma. Pediatric pulmonology 2014;49:1-7.

 

Massie J, Castellani C, Grody WW. Carrier screening for cystic fibrosis in the new era of medications that restore CFTR function. Lancet 2014;383:923-5.

 

Ioannou L, McClaren BJ, Massie J, et al. Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research. Genetics in medicine: official journal of the American College of Medical Genetics 2014;16:207-16.

 

Ioannou L, Massie J, Lewis S, McClaren B, Collins V, Delatycki MB. 'No thanks'-reasons why pregnant women declined an offer of cystic fibrosis carrier screening. Journal of community genetics 2014;5:109-17.

 

Ioannou L, Massie J, Lewis S, Collins V, McClaren B, Delatycki MB. Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening. European journal of human genetics: EJHG 2014;22:859-65.

 

Gu Y, Garcia-Perez S, Massie J, van Gool K. Cost of care for cystic fibrosis: an investigation of cost determinants using national registry data. The European journal of health economics: HEPAC : health economics in prevention and care 2014.

 

Elkins MR, Robinson P, Anderson SD, Perry CP, Daviskas E, Charlton B. Inspiratory flows and volumes in subjects with cystic fibrosis using a new dry powder inhaler device. The open respiratory medicine journal 2014;8:1-7.

 

Delatycki MB, Burke J, Christie L, et al. Human genetics society of australasia position statement: population-based carrier screening for cystic fibrosis. Twin research and human genetics: the official journal of the International Society for Twin Studies 2014;17:578-83.

 

Cunningham F, Lewis S, Curnow L, Glazner J, Massie J. Respiratory physicians and clinic coordinators' attitudes to population-based cystic fibrosis carrier screening. Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society 2014;13:99-105.

 

Chmiel JF, Aksamit TR, Chotirmall SH, et al. Antibiotic management of lung infections in cystic fibrosis. II. Nontuberculous mycobacteria, anaerobic bacteria, and fungi. Annals of the American Thoracic Society 2014;11:1298-306.

 

Castellani C, Massie J. Newborn screening and carrier screening for cystic fibrosis: alternative or complementary? The European respiratory journal 2014;43:20-3.

 

Blau H, Linnane B, Carzino R, et al. Induced sputum compared to bronchoalveolar lavage in young, non-expectorating cystic fibrosis children. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2014;13:106-10.

 

Archibald AD, Massie J, Smith MJ, Dalton DG, du Sart D, Amor DJ. Population-based genetic carrier screening for cystic fibrosis in Victoria. The Medical journal of Australia 2014;200:205-6.

 

 

2013

Wong JK, Ranganathan SC, Hart E, Australian Respiratory Early Surveillance Team for Cystic F. Staphylococcus aureus in early cystic fibrosis lung disease. Pediatric pulmonology 2013;48:1151-9.

 

Ranganathan SC, Skoric B, Ramsay KA, et al. Geographical differences in first acquisition of Pseudomonas aeruginosa in cystic fibrosis. Annals of the American Thoracic Society 2013;10:108-14.

 

Mott LS, Park J, Gangell CL, et al. Distribution of early structural lung changes due to cystic fibrosis detected with chest computed tomography. The Journal of pediatrics 2013;163:243-8 e1-3.

 

Mott LS, Graniel KG, Park J, et al. Assessment of early bronchiectasis in young children with cystic fibrosis is dependent on lung volume. Chest 2013;144:1193-8.

 

Mott LS, Park J, Murray CP, Gangell CL, de Klerk NH, Robinson PJ, Robertson CF, Ranganathan SC, Sly PD, Stick SM, AREST CF. (2013) Authors' response. Thorax 68:106

 

Simpson SJ, Mott LS, Esther CR, Jr., Stick SM, Hall GL. Novel end points for clinical trials in young children with cystic fibrosis. Expert review of respiratory medicine 2013;7:231-43.

 

Shields L, Munns A, Taylor M, Priddis L, Park J, Douglas T, AREST-CF. Scoping review of the literature about family-centered care with caregivers of children with cystic fibrosis. Neonatal, Paediatric and Child Health Nursing, 2013; 16(3): 21-5

 

Stick S, Tiddens H, Aurora P, Gustafsson P, Ranganathan S, Robinson P, Rosenfeld M, Sly P, Ratjen F. Early intervention studies in infants and preschool children with cystic fibrosis: are we ready? Eur Respir J. 2013;42:527-38.

 

Sly PD, Gangell CL, Chen L, Ware RS, Ranganathan S, Mott LS, Murrap CP, Stick SM, on behalf of AREST CF. Risk Factors for Bronchiectasis in Children with Cystic Fibrosis. N Engl J Med. 2013;368:1963-70.

 

Zemanick ET, Harris JK, Wagner BD, et al. Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations. PloS one 2013;8:e62917.

 

Wong R, Wong M, Robinson PD, Fitzgerald DA. Omalizumab in the management of steroid dependent allergic bronchopulmonary aspergillosis (ABPA) complicating cystic fibrosis. Paediatric respiratory reviews 2013;14:22-4.

 

Vandeleur M, Massie J, Oliver M. Gastrostomy in children with cystic fibrosis and portal hypertension. Journal of pediatric gastroenterology and nutrition 2013;57:245-7.

 

van Gool K, Norman R, Delatycki MB, Hall J, Massie J. Understanding the costs of care for cystic fibrosis: an analysis by age and health state. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2013;16:345-55.

 

Rosenfeld M, Allen J, Arets BH, et al. An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age. Annals of the American Thoracic Society 2013;10:S1-S11.

 

McClaren BJ, Aitken M, Massie J, Amor D, Ukoumunne OC, Metcalfe SA. Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing. Genetics in medicine : official journal of the American College of Medical Genetics 2013;15:533-40.

 

Massie J, Delatycki MB. Cystic fibrosis carrier screening. Paediatric respiratory reviews 2013;14:270-5.

 

Loeve M, Krestin GP, Rosenfeld M, de Bruijne M, Stick SM, Tiddens HA. Chest computed tomography: a validated surrogate endpoint of cystic fibrosis lung disease? The European respiratory journal 2013;42:844-57.

 

Kidd TJ, Ramsay KA, Hu H, et al. Shared Pseudomonas aeruginosa genotypes are common in Australian cystic fibrosis centres. The European respiratory journal 2013;41:1091-100.

 

Beydon N, Robinson PD. Early intervention for newborns screened for cystic fibrosis. American journal of respiratory and critical care medicine 2013;188:409-10.

 

 

2012

Garratt LW, Wright AK, Ranganathan SC, Grigg J, Sly PD, AREST CF. (2012) Small macrophages are present in early childhood respiratory disease. J Cyst Fibros 11:201-8

 

Mott LS, Park J, Murray CP, et al. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT. Thorax 2012;67:509-16.

 

Martin B, Schechter MS, Jaffe A, Cooper P, Bell SC, Ranganathan S. Comparison of the US and Australian cystic fibrosis registries: the impact of newborn screening. Pediatrics 2012;129:e348-55.

 

Robinson PD, Latzin P, Verbanck S, Hall GL, Horsley A, Gappa M, Thamrin C, Arets HGM, Aurora P, Fuchs S, King GG, Lum S, Macleod K, Paiva M, Pillow J, Ranganathan S, Ratjen F, Singer F, Sonnappa S, Stocks J, Subbarao P, Thompson B and Gustafsson P. (2012) Consensus statement for inert gas washout measurement using multiple- and single-breath tests. Eur Respir J 41:507-522

 

Smith C, Winn A, Seddon P, Ranganathan S. A fat lot of good: balance and trends in fat intake in children with cystic fibrosis. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2012;11:154-7.

 

Sheehan J, Massie J, Hay M, et al. The natural history and predictors of persistent problem behaviours in cystic fibrosis: a multicentre, prospective study. Archives of disease in childhood 2012;97:625-31.

 

Robinson P, Schechter MS, Sly PD, et al. Clarithromycin therapy for patients with cystic fibrosis: a randomized controlled trial. Pediatric pulmonology 2012;47:551-7.

 

Norman R, van Gool K, Hall J, Delatycki M, Massie J. Cost-effectiveness of carrier screening for cystic fibrosis in Australia. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2012;11:281-7.

 

Loeve M, Hop WC, de Bruijne M, et al. Chest computed tomography scores are predictive of survival in patients with cystic fibrosis awaiting lung transplantation. American journal of respiratory and critical care medicine 2012;185:1096-103.

 

Griffiths AL, Wurzel DF, Robinson PJ, Carzino R, Massie J. Australian epidemic strain pseudomonas (AES-1) declines further in a cohort segregated cystic fibrosis clinic. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2012;11:49-52.

 

 

2011

Sutanto EN, Kicic A, Foo CJ, et al. Innate inflammatory responses of pediatric cystic fibrosis airway epithelial cells: effects of nonviral and viral stimulation. American journal of respiratory cell and molecular biology 2011;44:761-7.

 

Stutz MD, Gangell CL, Berry LJ, et al. Cyanide in bronchoalveolar lavage is not diagnostic for Pseudomonas aeruginosa in children with cystic fibrosis. The European respiratory journal 2011;37:553-8.

 

Ranganathan SC, Parsons F, Gangell C, et al. Evolution of pulmonary inflammation and nutritional status in infants and young children with cystic fibrosis. Thorax 2011;66:408-13.

 

Pillarisetti N, Williamson E, Linnane B, et al. Infection, inflammation, and lung function decline in infants with cystic fibrosis. American journal of respiratory and critical care medicine 2011;184:75-81.

 

Hall GL, Logie KM, Parsons F, et al. Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening. PloS one 2011;6:e23932.

 

Gangell C, Gard S, Douglas T, et al. Inflammatory responses to individual microorganisms in the lungs of children with cystic fibrosis. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America 2011;53:425-32.

 

Gangell C, Hall GL, AREST CF. (2011) Early detection of lung function abnormalities in young children with Cystic Fibrosis. Annal Respir Med 2:22-27

 

Stick SM, Sly PD. Exciting new clinical trials in cystic fibrosis: infants need not apply. American journal of respiratory and critical care medicine 2011;183:1577-8.

 

Sly PD, Ware RS, de Klerk N, Stick SM. Randomised controlled trials in cystic fibrosis: what, when and how? The European respiratory journal 2011;37:991-3.

 

McClaren BJ, Metcalfe SA, Amor DJ, Aitken M, Massie J. A case for cystic fibrosis carrier testing in the general population. The Medical journal of Australia 2011;194:208-9.

 

Hall GL, Stocks J. Intervention trials and ventilation distribution in mild cystic fibrosis lung disease: will it all come out in the wash? The European respiratory journal 2011;37:757-9.

 

 

2010

Thomson E, Brennan S, Senthilmohan R, et al. Identifying peroxidases and their oxidants in the early pathology of cystic fibrosis. Free radical biology & medicine 2010;49:1354-60.

 

Sturges NC, Wikstrom ME, Winfield KR, et al. Monocytes from children with clinically stable cystic fibrosis show enhanced expression of Toll-like receptor 4. Pediatric pulmonology 2010;45:883-9.

 

Pillarisetti N, Linnane B, Ranganathan S, Arest CF. Early bronchiectasis in cystic fibrosis detected by surveillance CT. Respirology 2010;15:1009-11.

 

Gangell CL, Hall GL, Stick SM, Sly PD, Arest CF. Lung function testing in preschool-aged children with cystic fibrosis in the clinical setting. Pediatric pulmonology 2010;45:419-33.

 

Douglas TA, Brennan S, Berry L, et al. Value of serology in predicting Pseudomonas aeruginosa infection in young children with cystic fibrosis. Thorax 2010;65:985-90.

 

Berry LJ, Shiel B, Garratt L, Sly PD, AREST CF. (2010) Stability of interleukin 8 and neutrophil elastase in bronchoalveolar lavage fluid following long-term storage. J Cyst Fibros 9:346-50

 

Garratt LW, Mistry V, Singh R, Kaur Sandhu J, Sheil B, Cooke MS, Sly PD, AREST CF. (2010) Interpretation of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine is adversely affected by methodological inaccuracies when using a commercial ELISA. Free Radic Biol Med 48:1460-4

 

Massie J, Curnow L, Gaffney L, Carlin J, Francis I. Declining prevalence of cystic fibrosis since the introduction of newborn screening. Archives of disease in childhood 2010;95:531-3.

 

Massie J. Persistent elevated tissue-transglutaminase in cystic fibrosis. Journal of paediatrics and child health 2010;46:210.

 

Ioannou L, Massie J, Collins V, McClaren B, Delatycki MB. Population-based genetic screening for cystic fibrosis: attitudes and outcomes. Public health genomics 2010;13:449-56.

 

Cugley K, Crawford N, Royle J, Elia S, Massie J. Immunisation rates of children with cystic fibrosis using the Australian Childhood Immunisation Register. Journal of paediatrics and child health 2010;46:768-71.

 

Castellani C, Massie J. Emerging issues in cystic fibrosis newborn screening. Current opinion in pulmonary medicine 2010;16:584-90.

 

Castellani C, Macek M, Jr., Cassiman JJ, et al. Benchmarks for cystic fibrosis carrier screening: a European consensus document. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2010;9:165-78.

 

 

2009

Stick SM, Brennan S, Murray C, et al. Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. The Journal of pediatrics 2009;155:623-8 e1.

 

Sly PD, Brennan S, Gangell C, et al. Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening. American journal of respiratory and critical care medicine 2009;180:146-52.

 

Mott LS, Gangell CL, Murray CP, Stick SM, Sly PD, Arest CF. Bronchiectasis in an asymptomatic infant with cystic fibrosis diagnosed following newborn screening. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2009;8:285-7.

 

Brennan S, Sly PD, Gangell CL, et al. Alveolar macrophages and CC chemokines are increased in children with cystic fibrosis. The European respiratory journal 2009;34:655-61.

 

Harwood DT, Kettle AJ, Brennan S, Winterbourn CC. (2009) Simultaneous determination of reduced glutathione, glutathione disulphide and glutathione sulphonamide in cells and physiological fluids by isotope dilution liquid chromotagraphy-tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci 877:3393-9.

 

Douglas TA, Brennan S, Gard S, et al. Acquisition and eradication of P. aeruginosa in young children with cystic fibrosis. The European respiratory journal 2009;33:305-11.

 

Ward C, Massie J, Glazner J, et al. Problem behaviours and parenting in preschool children with cystic fibrosis. Archives of disease in childhood 2009;94:341-7.

 

Robinson PD, Cooper P, Van Asperen P, Fitzgerald D, Selvadurai H. Using index of ventilation to assess response to treatment for acute pulmonary exacerbation in children with cystic fibrosis. Pediatric pulmonology 2009;44:733-42.

 

Perera E, Massie J, Phillips RJ. Treatment of acne with oral isotretinoin in patients with cystic fibrosis. Archives of disease in childhood 2009;94:583-6.

 

O'Riordan SM, Robinson PD, Donaghue KC, Moran A. Management of cystic fibrosis-related diabetes in children and adolescents. Pediatric diabetes 2009;10 Suppl 12:43-50.

 

Neville LA, Ranganathan SC. Vitamin D in infants with cystic fibrosis diagnosed by newborn screening. Journal of paediatrics and child health 2009;45:36-41.

 

Massie J, Petrou V, Forbes R, et al. Population-based carrier screening for cystic fibrosis in Victoria: the first three years experience. The Australian & New Zealand journal of obstetrics & gynaecology 2009;49:484-9.

 

Massie J. Carrier screening for cystic fibrosis. Lancet 2009;374:978; author reply.

 

 

2008

Linnane BM, Hall GL, Nolan G, et al. Lung function in infants with cystic fibrosis diagnosed by newborn screening. American journal of respiratory and critical care medicine 2008;178:1238-44.

 

Stick SM. (2008) Clinical trials in infants with cystic fibrosis detected following newborn screening. Paediatr Respir Rev 9:176-80.

 

Sly PD. (2008) Early detection of lung disease in CF: do we have the necessary techniques? Paediatr Respir Rev 9:149-50.

 

Ranganathan S, Linnane B, Nolan G, Gangell C, Hall G. Early detection of lung disease in children with cystic fibrosis using lung function. Paediatric respiratory reviews 2008;9:160-7.

 

Linnane B, Robinson P, Ranganathan S, Stick S, Murray C. Role of high-resolution computed tomography in the detection of early cystic fibrosis lung disease. Paediatric respiratory reviews 2008;9:168-74; quiz 74-5.

 

Brennan S, Gangell C, Wainwright C, Sly PD. (2008) Disease surveillance using bronchoalveolar lavage. Paediatr Respir Rev 9:151-9.


Radhakrishnan M, van Gool K, Hall J, Delatycki M, Massie J. Economic evaluation of cystic fibrosis screening: a review of the literature. Health policy 2008;85:133-47.


 Mishra A, Greaves R, Smith K, et al. Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals. The Journal of pediatrics 2008;153:758-63.


Hafen GM, Hurst C, Yearwood J, Smith J, Dzalilov Z, Robinson PJ. A new scoring system in Cystic Fibrosis: statistical tools for database analysis - a preliminary report. BMC medical informatics and decision making 2008;8:44.


Farrell PM, Rosenstein BJ, White TB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. The Journal of pediatrics 2008;153:S4-S14.

 

 

2007

Thamrin C, Gangell CL, Udomittipong K, Kusel MMH, Patterson H, Fukushima T, Schultz A, Hall GL, Stick SM, Sly PD. (2007) Assessment of bronchodilator responsiveness in preschool children using forced oscillations. Thorax 62:814-9.


Gangell CL, Horak F, Jr., Patterson HJ, Sly PD, Stick SM, Hall GL. Respiratory impedance in children with cystic fibrosis using forced oscillations in clinic. The European respiratory journal 2007;30:892-7.


Mishra A, Greaves R, Massie J. The limitations of sweat electrolyte reference intervals for the diagnosis of cystic fibrosis: a systematic review. The Clinical biochemist Reviews / Australian Association of Clinical Biochemists 2007;28:60-76.


Massie J, Forbes R, Dusart D, Bankier A, Delatycki MB. Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis. Journal of paediatrics and child health 2007;43:721-3.


Horak F, Jr., Moeller A, Singer F, et al. Longitudinal monitoring of pediatric cystic fibrosis lung disease using nitrite in exhaled breath condensate. Pediatric pulmonology 2007;42:1198-206.


Comeau AM, Accurso FJ, White TB, et al. Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report. Pediatrics 2007;119:e495-518.


Cipolli M, Castellani C, Wilcken B, et al. Pancreatic phenotype in infants with cystic fibrosis identified by mutation screening. Archives of disease in childhood 2007;92:842-6.


Bell SC, Robinson PJ. Exacerbations in cystic fibrosis: 2 . prevention. Thorax 2007;62:723-32.

 

 

2006

Winfield KR, Gard S, Kent GN, Sly PD, Brennan S. (2006) Assay for urinary desmosines in a healthy pre-pubertal population using an improved extraction technique. Ann Clin Biochem 43:146-52.


Moeller A, Horak F, Jr., Lane C, et al. Inducible NO synthase expression is low in airway epithelium from young children with cystic fibrosis. Thorax 2006;61:514-20.


Franklin PJ, Hall GL, Moeller A, Horak F, Jr., Brennan S, Stick SM. Exhaled nitric oxide is not reduced in infants with cystic fibrosis. The European respiratory journal 2006;27:350-3.


Sawyer SM, Cerritelli B, Carter LS, Cooke M, Glazner JA, Massie J. Changing their minds with time: a comparison of hypothetical and actual reproductive behaviors in parents of children with cystic fibrosis. Pediatrics 2006;118:e649-56.


Massie J, Curnow L, Tzanakos N, Francis I, Robertson CF. Markedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing. Archives of disease in childhood 2006;91:222-5.


Massie J, Cranswick N. Pharmacokinetic profile of once daily intravenous tobramycin in children with cystic fibrosis. Journal of paediatrics and child health 2006;42:601-5.


Massie J. Sweat testing for cystic fibrosis: How good is your laboratory? Journal of paediatrics and child health 2006;42:153-4.


Lewis S, Curnow L, Ross M, Massie J. Parental attitudes to the identification of their infants as carriers of cystic fibrosis by newborn screening. Journal of paediatrics and child health 2006;42:533-7.


Hafen GM, Ranganathan SC, Robertson CF, Robinson PJ. Clinical scoring systems in cystic fibrosis. Pediatric pulmonology 2006;41:602-17.

 

 

2005

Pitrez PM, Brennan S, Turner S, Sly PD. Nasal wash as an alternative to bronchoalveolar lavage in detecting early pulmonary inflammation in children with cystic fibrosis. Respirology 2005;10:177-82.


Martin AC, Laing IA, Zhang G, et al. CD14 C-159T and early infection with Pseudomonas aeruginosa in children with cystic fibrosis. Respiratory research 2005;6:63.


Brennan S, Hall GL, Horak F, et al. Correlation of forced oscillation technique in preschool children with cystic fibrosis with pulmonary inflammation. Thorax 2005;60:159-63.


Ranganathan SC, Robertson CF. Ventilation inhomogeneities in patients with cystic fibrosis: inappropriate reference data and errors? American journal of respiratory and critical care medicine 2005;172:645; author reply -6.


Mishra A, Greaves R, Massie J. The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era. The Clinical biochemist Reviews / Australian Association of Clinical Biochemists 2005;26:135-53.


Massie J, Clements B, Australian Paediatric Respiratory G. Diagnosis of cystic fibrosis after newborn screening: the Australasian experience--twenty years and five million babies later: a consensus statement from the Australasian Paediatric Respiratory Group. Pediatric pulmonology 2005;39:440-6.

 

 

1996-2004

Sly PD, Brennan S. Detecting early lung disease in cystic fibrosis: are current techniques sufficient? Thorax 2004;59:1008-10.


Stapleton D, Kerr D, Gurrin L, Sherriff J, Sly P. Height and weight fail to detect early signs of malnutrition in children with cystic fibrosis. Journal of pediatric gastroenterology and nutrition 2001;33:319-25.


Brennan S, Cooper D, Sly PD. Directed neutrophil migration to IL-8 is increased in cystic fibrosis: a study of the effect of erythromycin. Thorax 2001;56:62-4.


Stapleton DR, Gurrin LC, Zubrick SR, Silburn SR, Sherriff JL, Sly PD. What do children with cystic fibrosis and their parents know about nutrition and pancreatic enzymes? Journal of the American Dietetic Association 2000;100:1494-500.


Everard ML, Sly P, Brenan S, Ryan G. Macrolide antibiotics in diffuse panbronchiolitis and in cystic fibrosis. The European respiratory journal 1997;10:2926.

 

 

Last updated: May 2015