Key Publications

2018

The School Experiences of Siblings of Children With Chronic Illness: Australian Parents’ Perceptions, Gan LL; Lum A; Wakefield CE; Donnan BM; Marshall GM; Burns MA; Jaffe A; Leach S; Lemberg DA; Fardell JE, 2018, Educational and Developmental Psychologist, pp. 1 - 15

Probiotics for people with cystic fibrosis Coffey MJ; Garg M; Homaira N; Jaffe A; Ooi CY, 2018, Cochrane Database of Systematic Reviews, vol. 2018

Age-related levels of fecal M2-pyruvate kinase in children with cystic fibrosis and healthy children 0 to 10 years old, Garg M; Leach ST; Pang T; Needham B; Coffey MJ; Katz T; Strachan R; Widger J; Field P; Belessis Y; Chuang S; Day AS; Jaffe A; Ooi CY, 2018, Journal of Cystic Fibrosis, vol. 17, pp. 109 - 113

2017

Rare disease registries: a call to action, Lacaze P; Millis N; Fookes M; Zurynski Y; Jaffe A; Bellgard M; Winship I; McNeil J; Bittles AH, 2017, Internal Medicine Journal, vol. 47, pp. 1075 - 1079

Age-dependent variation of fecal calprotectin in cystic fibrosis and healthy children, Garg M; Leach ST; Coffey MJ; Katz T; Strachan R; Pang T; Needham B; Lui K; Ali F; Day AS; Appleton L; Moeeni V; Jaffe A; Ooi CY, 2017, Journal of Cystic Fibrosis, vol. 16, pp. 631 - 636,

Association of rhinovirus with exacerbations in young children affected by cystic fibrosis: Preliminary data, Stelzer-Braid S; Liu N; Doumit M; D'Cunha R; Belessis Y; Jaffe A; Rawlinson WD, 2017, Journal of Medical Virology, vol. 89, pp. 1494 - 1497,

2016

Question 5: What is the role of macrolide antibiotics as anti-inflammatory treatment in Cystic fibrosis?, Fitzgerald NM; Jaffe A, 2016, Paediatric Respiratory Reviews, vol. 18, pp. 55 - 57

Resolution of intestinal histopathology changes in cystic fibrosis after treatment with ivacaftor, Safe M; Gifford AJ; Jaffe A; Ooi CY, 2016, Annals of the American Thoracic Society, vol. 13, pp. 297 - 298

Is there a role for stool metabolomics in cystic fibrosis?, Kaakoush NO; Pickford R; Jaffe A; Ooi CY, 2016, Pediatrics International, vol. 58, pp. 808 - 811

Diagnosing cystic fibrosis-related diabetes: current methods and challenges, Prentice B; Hameed S; Verge CF; Ooi CY; Jaffe A; Widger J , 2016, Expert Review of Respiratory Medicine, vol. 10, pp. 799 - 811

Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis Nielsen S; Needham B; Leach ST; Day AS; Jaffe A; Thomas T; Ooi CY, 2016, Scientific Reports, vol. 6

Diagnostic accuracy and distress associated with oropharyngeal suction in cystic fibrosis, Doumit M; Belessis Y; Stelzer-Braid S; Mallitt KA; Rawlinson W; Jaffe A, 2016, Journal of Cystic Fibrosis, vol. 15, pp. 473 - 478,

2015

A pilot study of inhaled dry-powder mannitol during cystic fibrosis-related pulmonary exacerbation, Middleton A; Robinson PD; McKay K; Jaffe A; Selvadurai H, 2015, European Respiratory Journal, vol. 45, pp. 541 - 544,

Advances in the detection and management of cystic fibrosis related diabetes, Hameed S; Jaffé A; Verge CF, 2015, Current Opinion in Pediatrics, vol. 27, pp. 525 - 533