Adelaide Research & Scholarship: Search

Search

Search:
for

Current filters:

Start a new search

Add filters:

Results/Page | Sort items by In order Authors/record

Results 61-70 of 145 (Search time: 0.002 seconds).

previous
1
...
4
5
6
7
8
9
10
...
15
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2003	Frontoethmoidal encephalomeningocele: new morphological findings and a new classification	Rojvachiranonda, N.; David, D.; Moore, M.; Cole, J.
	2002	ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation	Bienvenu, T.; Poirier, K.; Friocourt, G.; Bahi, N.; Beaumont, D.; Fauchereau, F.; Jeema, L.; Zemni, R.; Vinet, M.; Francis, F.; Couvert, P.; Gomot, M.; Moraine, C.; van Bokhoven, H.; Kalscheuer, V.; Frints, S.; Gecz, J.; Ohzaki, K.; Chaabouni, H.; Fryns, J.; et al.
	2006	Long-term outcome of skull base surgery with microvascular reconstruction for malignant disease	Nouraei, S.; Ismail, Y.; Gerber, C.; Crawford, P.; McLean, N.; Hodgkinson, P.
	2002	Effect of changes in antibiotic prescribing on patient outcomes in a community setting: A natural experiment in Australia	Beilby, J.; Marley, J.; Walker, D.; Chamberlain, N.; Burke, M.
	2002	National study of adverse reactions after vaccination with bacille Calmette-Guérin	Turnbull, F.; McIntyre, P.; Achat, H.; Wang, H.; Stapledon, R.; Gold, M.; Burgess, M.
	2007	Acute lung injury in pediatric intensive care in Australia and New Zealand - A prospective, multicenter, observational study	Erickson, S.; Schibler, A.; Numa, A.; Nuthall, G.; Yung, M.; Pascoe, E.; Wilkins, B.
	2009	An audit of first aid treatment of paediatric burns patients and their clinical outcome	Cuttle, L.; Kravchuk, O.; Wallis, B.; Kimble, R.
	2007	Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutations	Scheffer, I.; Harkin, L.; Grinton, B.; Dibbens, L.; Turner, S.; Zielinski, M.; Xu, R.; Jackson, G.; Adams, J.; Connellan, M.; Petrou, S.; Wellard, R.; Briellmann, R.; Wallace, R.; Mulley, J.; Berkovic, S.
	2007	Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor	Ali, A.; Christie, P.; Grigorieva, I.; Harding, B.; Van Esch, H.; Ahmed, S.; Bitner-Glindzicz, M.; Blind, E.; Bloch, C.; Christin, P.; Clayton, P.; Gecz, J.; Gilbert-Dussardier, B.; Guillen-Navarro, E.; Hackett, A.; Halac, I.; Hendy, G.; Lalloo, F.; Mache, C.; Mughal, Z.; et al.
	2002	Axonal injury in children after motor vehicle crashes: Extent, distribution, and size of axonal swellings using b-APP immunohistochemistry	Gorrie, C.; Oakes, S.; Duflou, J.; Blumbergs, P.; Waite, P.