Dr Didu Kariyawasam
BA, MA(Cantab), MRCPCH, RACP, PhD
Dr Didu (Sandi) Kariyawasamn is a paediatric neurologist, and post doctoral researcher at 黑料网大事记 Sydney. She听completed her Masters at the University of Cambridge, UK, subsequently graduating from University College London in 2007. She embarked on her training in Paediatric Neurology at John Radcliffe Hospital, Oxford, UK, gaining specialist expertise in the management of complex epilepsy (Great Ormond Street Hospital, London), movement disorders (Evelina Children鈥檚 Hospital London) and neuroinflammation (John Radcliffe Hospital, Oxford). In 2022, Sandi successfully completed a PhD in the investigation of pathways to optimise diagnosis and care for children with Neurogenetic disease.
Sandi currently practices clinically at Sydney Children鈥檚 Hospital (Randwick), and as an early career researcher, holds the title of associate lecturer at the University of New South Wales. She recently completed her PhD (2022),听evaluating the novel diagnostic and management pathways in paediatric neuromuscular disease (NMD).听
Sandi is active in the field of clinical trials and is part of the clinical research team providing access to new genetic therapies in the field of childhood onset neurological disease. Her work has been translational in the domain of paediatric neuromuscular disease where she strives to improve health and psychosocial outcomes for affected children and their families.听
Sandi's goal is to provide optimal care and informed choice for families, based on best current evidence, taking into account the values and beliefs of the individual. The ethos that underpins her work is maintaining a child- and family-centred focus to improve the health and well-being of her patients.
- Publications
- Media
- Grants
- Awards
- Research Activities
- Engagement
- Teaching and Supervision
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黑料网大事记 Paediatric Research Week Annual Prize (2019)
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ANZCNS Best Research Award (2020)
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Brain Foundation Grant (2021).
Publications听
1.听Kariyawasam DST, Russell JS, Wiley V, Alexander IE, Farrar MA. The implementation of newborn screening for spinal muscular atrophy: the Australian experience.听Genet Med. 2020;22(3):557-565. doi:10.1038/s41436-019-0673-0
2. Kariyawasam DST, D'Silva A, Lin C, Ryan MM, Farrar MA. Biomarkers and the Development of a Personalized Medicine Approach in Spinal Muscular Atrophy.听Front Neurol. 2019;10:898. Published 2019 Aug 19. doi:10.3389/fneur.2019.00898
3.听Didu Kariyawasam, Kate A. Carey, Kristi J. Jones, Michelle A. Farrar. New and developing therapies in spinal muscular atrophy. Paediatric Respiratory Reviews. 2018. https://doi.org/10.1016/j.prrv.2018.03.003.
4.听Kariyawasam听D,听Alexander听IE,听Kurian听M, et al. Great expectations: virus-mediated gene therapy in neurological disorders. Journal of Neurology, Neurosurgery & Psychiatry听2020;91:849-860.
5.听D'Silva AM, Holland S, Kariyawasam D, et al. Onasemnogene abeparvovec in spinal muscular atrophy: an Australian experience of safety and efficacy.听Ann Clin Transl Neurol. 2022;9(3):339-350. doi:10.1002/acn3.51519
6.听D'Silva AM, Kariyawasam DST, Best S, Wiley V, Farrar MA; NSW SMA NBS Study Group. Integrating newborn screening for spinal muscular atrophy into health care systems: an Australian pilot programme.听Dev Med Child Neurol. 2022;64(5):625-632. doi:10.1111/dmcn.15117
7.听Kariyawasam D, D'Silva A, Howells J, et al. Motor unit changes in children with symptomatic spinal muscular atrophy treated with nusinersen [published online ahead of print, 2020 Oct 26].听J Neurol Neurosurg Psychiatry. 2020;92(1):78-85. doi:10.1136/jnnp-2020-324254
8.听Kariyawasam, D., D鈥橲ilva, A., Mowat, D.听et al.听Incidence of Duchenne muscular dystrophy in the modern era; an Australian study.听Eur J Hum Genet听30, 1398鈥1404 (2022). https://doi.org/10.1038/s41431-022-01138-2
9. Kariyawasam DST, D'Silva AM, Vetsch J, Wakefield CE, Wiley V, Farrar MA. "We needed this": perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy.听EClinicalMedicine. 2021;33:100742. Published 2021 Feb 19. doi:10.1016/j.eclinm.2021.100742
10.听Kariyawasam DS, D'Silva AM, Sampaio H, et al. Newborn screening for spinal muscular atrophy in Australia: a non-randomised cohort study [published online ahead of print, 2023 Jan 17].听Lancet Child Adolesc Health. 2023;S2352-4642(22)00342-X. doi:10.1016/S2352-4642(22)00342-X
11.听Kariyawasam DST, D'Silva AM, Herbert K, et al. Axonal excitability changes in children with spinal muscular atrophy treated with nusinersen.听J Physiol. 2022;600(1):95-109. doi:10.1113/JP282249
12.听Nguyen CQ, Kariyawasam D, Alba-Concepcion K, et al. 'Advocacy groups are the connectors': Experiences and contributions of rare disease patient organization leaders in advanced neurotherapeutics.听Health Expect. 2022;25(6):3175-3191. doi:10.1111/hex.13625
13. D'Silva AM, Kariyawasam D, Venkat P, Mayoh C, Farrar MA. Identification of Novel CSF-Derived miRNAs in Treated Paediatric Onset Spinal Muscular Atrophy: An Exploratory Study.听Pharmaceutics. 2023;15(1):170. Published 2023 Jan 3. doi:10.3390/pharmaceutics15010170
14.听Farrar MA, Kariyawasam D, Grattan S, et al. Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy.听J Neuromuscul Dis. 2023;10(1):15-28. doi:10.3233/JND-221535
15.听Kariyawasam DS, McShane T. Brain tumours in paediatrics: when should they be suspected?.听Arch Dis Child. 2015;100(12):1102-1103. doi:10.1136/archdischild-2015-308729
16.听Kariyawasam听DS,听Samapio听H,听Mowat听D, et al. Genetic carrier screening for duchenne muscular dystrophy: the outcome of over twenty years of genetic counselling on disease epidemiology in a single-centre cohort study in new south wales (NSW), Australia. Journal of Neurology, Neurosurgery & Psychiatry听2019;90:A8-A9.
17.听Anand听G,听Vasallo听G,听Spanou听M,..., Kariyawasam DS, et al. Diagnosis of sporadic neurofibromatosis type 2 in the paediatric population. Archives of Disease in Childhood听2018;103:463-469.
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Society Memberships & Professional Activities:
- Member of the Royal College of Paediatrics and Child Health, UK听
- Royal Australasian College of Physicians听