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News & Events
Diabetes clinic: We've movedWith a little over a week before outpatient clinics move from Princess Margaret Hospital (PMH) to Perth Children’s Hospital (PCH), now is the time to familiarise yourself with all the information you need to know before you make your first visit.
Research
Use of Hybrid Closed Loop therapy in hypoglycaemia awarenessThis study will tell us if the use of a hybrid closed loop system can improve awareness of hypoglycaemia.
Research
Is sport an untapped resource for recovery from first episode psychosis? A narrative review and call to actionSport-based interventions could be an opportunity to provide intervention to individuals recovering from their first psychotic episode
Research
Age at diagnosis of birth defectsMany birth defects surveillance programs ascertain cases of birth defects diagnosed beyond 1 year of age.
Besides the challenges associated with their teenage years, adolescents with Type 1 Diabetes (T1D) encounter additional challenges of having a chronic condition.
News & Events
Combating glucose rises after meals - new studyParticipants are needed for a new Children's Diabates Centre study looking at the patterns in glucose rise after meals.
News & Events
Family’s fundraising efforts a hole-in-oneWhen Meghan Bunter’s daughter was first diagnosed with diabetes, she felt overwhelmed not only with Ella’s diagnosis but also the flood of donation requests.
News & Events
Diabetes in Schools updateDo you know that the clinical team at Perth Children’s Hospital’s Diabetes Clinic can visit your child’s school to administer glucagon or camp education?
Research
Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 yearsWe report data from the interim analysis of the ongoing VIVIANE study, the aim of which is to assess the efficacy, safety, and immunogenicity of the HPV...
Research
An evaluation of GPT models for phenotype concept recognitionClinical deep phenotyping and phenotype annotation play a critical role in both the diagnosis of patients with rare disorders as well as in building computationally-tractable knowledge in the rare disorders field.