Lauren J Rice
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Explore the profile of Lauren J Rice including associated specialties, affiliations and a list of published articles.
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19
Citations
161
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Recent Articles
1.
Rice L, Agu J, Carter C, Cho Y, Harris J, Heilman K, et al.
Int J Psychophysiol
. 2024 Sep;
205:112429.
PMID: 39237036
This study aimed to increase our understanding of cardiac activity abnormalities in Prader-Willi Syndrome (PWS) and the relationship between cardiac activity, PWS behaviours thought to be associated with cardiac vagal...
2.
Stubbs T, Cannon L, Carter E, Naanai H, Okurame J, Martiniuk A, et al.
BMJ Open
. 2024 Jul;
14(7):e086999.
PMID: 39002966
Objectives: This scoping review aimed to identify and critically appraise resources for health professionals to identify, diagnose, refer, and support individuals with fetal alcohol spectrum disorder (FASD)-including the extent to...
3.
Rice L, Agu J, Carter C, Harris J, Nazarloo H, Naanai H, et al.
Front Endocrinol (Lausanne)
. 2023 Jun;
14:1183525.
PMID: 37313445
Background: Oxytocin and vasopressin systems are altered in Prader Willi syndrome (PWS). However, investigations into endogenous oxytocin and vasopressin levels as well as clinical trials evaluating the effect of exogenous...
4.
Rice L, Cannon L, Dadlani N, Cheung M, Einfeld S, Efron D, et al.
Eur Child Adolesc Psychiatry
. 2023 Mar;
33(2):505-526.
PMID: 36864363
A better understanding of the endocannabinoid system and a relaxation in regulatory control of cannabis globally has increased interest in the medicinal use of cannabinoid-based products (CBP). We provide a...
5.
Shields N, Bennell K, Southby A, Rice L, Markovic T, Bigby C, et al.
BMJ Open
. 2022 Dec;
12(12):e060306.
PMID: 36549735
Introduction: Preliminary evidence suggests that progressive resistance training may be beneficial for people with Prader-Willi Syndrome (PWS), a rare genetic condition that results in muscle weakness and low muscle tone.To...
6.
McAlary L, Shephard V, Sher M, Rice L, Yerbury J, Cashman N, et al.
STAR Protoc
. 2022 Oct;
3(4):101748.
PMID: 36201320
Proteinaceous inclusions are associated with neurodegenerative diseases and cell models are often used to determine genetic and chemical modifiers of their formation. This protocol involves the usage of automated microscopy...
7.
Okurame J, Cannon L, Carter E, Thomas S, Elliott E, Rice L
BMJ Open
. 2022 Sep;
12(9):e065327.
PMID: 36100303
Introduction: People with fetal alcohol spectrum disorder (FASD) encounter a range of health and allied health providers and require specialised support to ensure health services are provided safely and effectively....
8.
Rice L, Tsang T, Carter E, Hand M, Davies J, Thomas S, et al.
BMJ Open
. 2022 Apr;
12(4):e058111.
PMID: 35365538
Introduction: The Lililwan Project was the first Australian population-based prevalence study of fetal alcohol spectrum disorder (FASD) using active case ascertainment. Conducted in 2010-2011, the study included 95% of all...
9.
Lees B, Riches J, Mewton L, Elliott E, Allsop S, Newton N, et al.
Health Promot J Austr
. 2022 Jan;
33(3):797-809.
PMID: 35028999
Children with foetal alcohol spectrum disorder (FASD) can experience neurodevelopmental, physical, psychological and behavioural impairments that can result in a disrupted school experience. However, educators often have limited knowledge or...
10.
Rice L, Ecroyd H, van Oijen A
Comput Struct Biotechnol J
. 2021 Sep;
19:4711-4724.
PMID: 34504664
The aggregation of proteins into insoluble filamentous amyloid fibrils is a pathological hallmark of neurodegenerative diseases that include Parkinson's disease and Alzheimer's disease. Since the identification of amyloid fibrils and...