Detalhe da pesquisa
1.
Evaluation of mild periorbital cellulitis and home-based therapy in children-EPOCH study: A prospective single centre cohort study.
Clin Exp Ophthalmol
; 51(5): 462-471, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37143401
2.
Assessing the adherence to guidelines in the management of croup in Australian children: a population-based sample survey.
Int J Qual Health Care
; 31(10): 759-767, 2019 Dec 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31665290
3.
Bell's Palsy in Children (BellPIC): protocol for a multicentre, placebo-controlled randomized trial.
BMC Pediatr
; 17(1): 53, 2017 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-28193257
4.
Pain in children with Bell's palsy: secondary analysis of a randomised controlled trial.
Arch Dis Child
; 109(3): 227-232, 2024 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38049992
5.
Facial Function in Bell Palsy in a Cohort of Children Randomized to Prednisolone or Placebo 12 Months After Diagnosis.
Pediatr Neurol
; 153: 44-47, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38320457
6.
Agreement Between House-Brackmann and Sunnybrook Facial Nerve Grading Systems in Bell's Palsy in Children: Secondary Analysis of a Randomized, Placebo-Controlled Multicenter Trial.
J Child Neurol
; 38(1-2): 44-51, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36740927
7.
Efficacy of Prednisolone for Bell Palsy in Children: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial.
Neurology
; 2022 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36008143
8.
Treatment patterns and frequency of key outcomes in acute severe asthma in children: a Paediatric Research in Emergency Departments International Collaborative (PREDICT) multicentre cohort study.
BMJ Open Respir Res
; 9(1)2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35301198
9.
Out-of-hospital arrests attending an Australian tertiary paediatric emergency department over 13 years: An observational study.
Emerg Med Australas
; 30(5): 687-693, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30021244
10.
An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies.
Am J Med Genet A
; 143A(20): 2452-9, 2007 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17853472