WS9.6 Cystic fibrosis-related postural and baropodometric changes: A comparison with healthy individuals
Autor: | R.R. Batista, Patricia Xavier Hommerding, Denizar Alberto da Silva Melo, P.J. Marostica, Cláudia Silva Schindel, Márcio Vinícius Fagundes Donadio |
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Jazyk: | angličtina |
Předmět: |
Pulmonary and Respiratory Medicine
medicine.medical_specialty business.industry medicine.medical_treatment Medical school medicine.disease Cystic fibrosis law.invention Respiratory Medicine Randomized controlled trial law Healthy individuals Pediatrics Perinatology and Child Health Physical therapy Medicine Pediatrics Perinatology and Child Health business human activities Saline |
Zdroj: | Journal of Cystic Fibrosis. :S19 |
ISSN: | 1569-1993 |
DOI: | 10.1016/S1569-1993(13)60057-0 |
Popis: | WS9.5 Saline at lower tonicity in cystic fibrosis (SALTI-CF) trial − A randomised, controlled trial comparing 0.9% v 3% v 6% nebulised saline T. Dwyer1,2, M. Elkins1,2, R. Dentice1,2,3, S. Forbes4, M. Mcarthur4, P. Cooper4, A. Jaffe5,6, P. Middleton1,7, P. Wark8, P. Bye1,2, SALTI-CF Study Group. 1University of Sydney, Sydney Medical School, Sydney, Australia; 2Royal Prince Alfred Hospital, Respiratory Medicine, Sydney, Australia; 3Royal Prince Alfred Hospital, Physiotherapy, Sydney, Australia; 4Children’s Hospital Westmead, Respiratory Medicine, Sydney, Australia; 5University of New South Wales, School of Women’s and Children’s Health, Sydney, Australia; 6Sydney Children’s Hospital, Respiratory Medicine, Sydney, Australia; 7Westmead Hospital, Respiratory Medicine, Sydney, Australia; 8John Hunter Hospital, Respiratory Medicine, Newcastle, Australia |
Databáze: | OpenAIRE |
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