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Preview	Issue Date	Title	Author(s)
	2021	Different types of disease-causing non-coding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability	Field, M.J.; Sharma, R.; Hackett, A.; Kayumi, S.; Shoubridge, C.; Ewans, L.J.; Ivancevic, A.M.; Dudding-Byth, T.; Carroll, R.; Kroes, T.; Gardner, A.E.; Sullivan, P.; Ha, T.T.; Schwartz, C.E.; Cowley, M.J.; Dinger, M.E.; Palmer, E.E.; Christie, L.; Shaw, M.; Roscioli, T.; et al.
	2023	Randomized Trial of BCG Vaccine to Protect against Covid-19 in Health Care Workers	Pittet, L.F.; Messina, N.L.; Orsini, F.; Moore, C.L.; Abruzzo, V.; Barry, S.; Bonnici, R.; Bonten, M.; Campbell, J.; Croda, J.; Dalcolmo, M.; Gardiner, K.; Gell, G.; Germano, S.; Gomes-Silva, A.; Goodall, C.; Gwee, A.; Jamieson, T.; Jardim, B.; Kollmann, T.R.; et al.
	2021	Prospective characterisation of SARS-CoV-2 infections among children presenting to tertiary paediatric hospitals across Australia in 2020: a national cohort study	Wurzel, D.; McMinn, A.; Hoq, M.; Blyth, C.C.; Burgner, D.; Tosif, S.; Buttery, J.; Carr, J.; Clark, J.E.; Cheng, A.C.; Dinsmore, N.; Francis, J.R.; Kynaston, A.; Lucas, R.; Marshall, H.; McMullan, B.; Singh-Grewal, D.; Wood, N.; Macartney, K.; Britton, P.N.; et al.
	2022	Longitudinal audit of assessment and pharmaceutical intervention for cardiovascular risk in the Australasian Diabetes Data Network	Robertson, C.A.; Earnest, A.; Chee, M.; Craig, M.E.; Colman, P.; Barrett, H.L.; Bergman, P.; Cameron, F.; Davis, E.E.; Donaghue, K.C.; Fegan, P.G.; Hamblin, P.S.; Holmes-Walker, D.J.; Jefferies, C.; Johnson, S.; Mok, M.T.; King, B.R.; Sinnott, R.; Ward, G.; Wheeler, B.J.; et al.
	2022	Management of paediatric acute severe behavioural disturbance in emergency departments across Australia: A PREDICT survey of senior medical staff	Bourke, E.M.; Knott, J.C.; Craig, S.; Babl, F.E.; Babl, F.; Beattie, A.; Borland, M.; Bourke, E.; Buntine, P.; Craig, S.; Gamage, L.; George, S.; Ghedina, N.; Furyk, J.; Halkidis, L.; Hort, J.; King, A.; Kochar, A.; Lithgow, A.; McKenzie, B.; et al.
	2023	A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome	Walker, R.; Mahmood, K.; Joo, J.E.; Clendenning, M.; Georgeson, P.; Como, J.; Joseland, S.; Preston, S.G.; Antill, Y.; Austin, R.; Boussioutas, A.; Bowman, M.; Burke, J.; Campbell, A.; Daneshvar, S.; Edwards, E.; Gleeson, M.; Goodwin, A.; Harris, M.T.; Henderson, A.; et al.
	2022	Probiotic peanut oral immunotherapy versus oral immunotherapy and placebo in children with peanut allergy in Australia (PPOIT-003): a multicentre, randomised, phase 2b trial	Loke, P.; Orsini, F.; Lozinsky, A.C.; Gold, M.; O'Sullivan, M.D.; Quinn, P.; Lloyd, M.; Ashley, S.E.; Pitkin, S.; Axelrad, C.; Metcalfe, J.R.; Su, E.L.; Tey, D.; Robinson, M.N.; Allen, K.J.; Prescott, S.L.; Galvin, A.D.; Tang, M.L.K.; O'Sullivan, M.; Fahy-Scheer, S.; et al.
	2023	Bi-allelic variants in the neuronal cell adhesion molecule NRCAM lead to a novel neurodevelopmental disorder characterized by developmental delay, hypotonia, peripheral neuropathy or spasticity	Kurolap, A.; Kreuder, F.; Gonzaga-Jauregui, C.; Duvdevani, M.P.; Harel, T.; Tammer, L.; Xin, B.; Bakhtiari, S.; Rice, J.; van Eyk, C.; Gecz, J.; Mah, J.K.; Atkinson, D.; Cope, H.; Sullivan, J.A.; Douek, A.M.; Colquhoun, D.; Henry, J.; Wlodkowic, D.; Parman, Y.; et al.; 55th European Society of Human Genetics Conference (ESHG) (11 Jun 2022 - 14 Jun 2022 : Vienna, Austria & virtual online)
	2024	Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment	Bhattacharjee, R.; Jolly, L.A.; Corbett, M.A.; Wee, I.C.; Rao, S.R.; Gardner, A.E.; Ritchie, T.; van Hugte, E.J.H.; Ciptasari, U.; Piltz, S.; Noll, J.E.; Nazri, N.; van Eyk, C.L.; White, M.; Fornarino, D.; Poulton, C.; Baynam, G.; Collins-Praino, L.E.; Snel, M.F.; Nadif Kasri, N.; et al.