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Preview	Issue Date	Title	Author(s)
	2007	Improving patient satisfaction through information provision	Billing, K.; Newland, H.; Selva-Nayagam, D.
	2000	Open invitation from the International Poverty and Health Network to all healthcare professionals	Heath, I.; Haines, A.; Glover, J.; Hetzel, D.
	2008	TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness	Guipponi, M.; Antonarakis, S.; Scott, H.
	2006	Prevalence of trachoma among a group of Aboriginal school children in remote South Australia	Durkin, S.; Casson, R.; Selva-Nayagam, D.; Newland, H.
	2001	Use of inhaled anti-inflammatory medication in children with asthma in managed care settings	Adams, R.; Fuhlbrigge, A.; Finkelstein, J.; Lozano, P.; Livingston, J.; Weiss, K.; Weiss, S.
	2020	Contemporary Incidence and Prevalence of Rheumatic Fever and Rheumatic Heart Disease in Australia Using Linked Data: The Case for Policy Change	Katzenellenbogen, J.M.; Bond-Smith, D.; Seth, R.J.; Dempsey, K.; Cannon, J.; Stacey, I.; Wade, V.; de Klerk, N.; Greenland, M.; Sanfilippo, F.M.; Brown, A.; Carapetis, J.R.; Wyber, R.; Nedkoff, L.; Hung, J.; Bessarab, D.; Ralph, A.P.
	2023	The unfinished agenda of communicable diseases among children and adolescents before the COVID-19 pandemic, 1990–2019: a systematic analysis of the Global Burden of Disease Study 2019	Sharew, N.T.
	2019	Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2	Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.
	2019	Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission	Guo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
	2019	Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia	Gorman, K.M.; Meyer, E.; Grozeva, D.; Spinelli, E.; McTague, A.; Sanchis-Juan, A.; Carss, K.J.; Bryant, E.; Reich, A.; Schneider, A.L.; Pressler, R.M.; Simpson, M.A.; Debelle, G.D.; Wassmer, E.; Morton, J.; Sieciechowicz, D.; Jan-Kamsteeg, E.; Paciorkowski, A.R.; King, M.D.; Cross, J.H.; et al.