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Preview	Issue Date	Title	Author(s)
	1995	Expression, purification and characterization of recombinant human N-acetylgalactosamine-6-sulphatase	Bielicki, J.; Fuller, M.; Guo, X.; Morris, C.; Hopwood, J.; Anson, D.
	1997	Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cells	Ferrara, M.; Occhiodoro, T.; Fuller, M.; Hawthorne, W.; Teutsch, S.; Tucker, V.; Hopwood, J.; Stewart, G.; Anson, D.
	2016	Cryopyrin-associated periodic syndrome in Australian children and adults: epidemiological, clinical and treatment characteristics	Mehr, S.; Allen, R.; Boros, C.; Adib, N.; Kakakios, A.; Turner, P.; Rogers, M.; Zurynski, Y.; Singh-Grewal, D.
	2018	The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registry	Girschick, H.; Finetti, M.; Orlando, F.; Schalm, S.; Insalaco, A.; Ganser, G.; Nielsen, S.; Herlin, T.; Koné-Paut, I.; Martino, S.; Cattalini, M.; Anton, J.; Al-Mayouf, S.; Hofer, M.; Quartier, P.; Boros, C.; Kuemmerle-Deschner, J.; Pires Marafon, D.; Alessio, M.; Schwarz, T.; et al.
	2014	Associations of circulating calcium and 25-hydroxyvitamin D with glucose metabolism in pregnancy: a cross-sectional study in European and south Asian women	Whitelaw, D.; Scally, A.; Tuffnell, D.; Davies, T.; Fraser, W.; Bhopal, R.; Wright, J.; Lawlor, D.
	1998	Transcranial correction of orbital neurofibromatosis	Snyder, B.; Hanieh, A.; Trott, J.; David, D.
	2000	No evidence for association of 5-HT2A receptor polymorphism with suicide	Crawford, J.; Sutherland, G.; Goldney, R.
	2006	Newborn screening for 3-methylcrontonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment	Stadler, S.; Polanetz, R.; Maier, E.; Heidenreich, S.; Niederer, B.; Mayerhofer, P.; Lagler, F.; Koch, H.; Santer, R.; Fletcher, J.; Ranieri, E.; Das, A.; Spiekerkotter, U.; Schwab, K.; Potzsch, S.; Marquardt, I.; Hennermann, J.; Knerr, I.; Mercimek-Mahmutoglu, S.; Kohlschmidt, N.; et al.
	2015	High incidence of Noonan Syndrome features including short stature and pulmonic stenosis in patients carrying NF1 missense mutations affecting p.Arg1809: genotype-phenotype correlation	Rojnueangnit, K.; Xie, J.; Gomes, A.; Sharp, A.; Callens, T.; Chen, Y.; Liu, Y.; Cochran, M.; Abbott, M.; Atkin, J.; Babovic-Vuksanovic, D.; Barnett, C.; Crenshaw, M.; Bartholomew, D.; Basel, L.; Bellus, G.; Ben-Shachar, S.; Bialer, M.; Bick, D.; Blumberg, B.; et al.
	2003	The new medical malpractice crisis	Couper, R.