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Research
Prednisolone Versus Dexamethasone for Croup: a Randomized Controlled TrialThe type of oral steroid seems to have no clinically significant impact on efficacy, both acutely and during the week after treatment
Research
Severe hypoglycemia rates are not associated with HbA1c: A cross-sectional analysis of 3 contemporary pediatric diabetes registry databasesTo examine the association between glycated hemoglobin (HbA1c) and severe hypoglycemia rates in patients with type 1 diabetes receiving usual care.
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.
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.
Read about the research fellows at the Children's Diabetes Centre, Martin de Bock, Aveni Hayes, Ashleigh Lin and Marie-Anne Burckhardt.
News & Events
Dr Shaun Teo and Dr Paul Fournier awarded Diabetes Australia grantsA big congratulations to our The Kids and UWA researchers Dr Shaun Teo and Dr Paul Fournier who have both been awarded $70,000 grants for their diabetes research projects, under the 2023 Diabetes Australia Research Program (DARP).
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.