Adelaide Research & Scholarship: Search

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Preview	Issue Date	Title	Author(s)
	1997	The spectrum of primary immundeficiency disorders in Australia	Baumgart, K.; Britton, W.; Kemp, A.; French, M.; Roberton, D.
	2000	Randomized trial of omeprazole and metronidazole with amoxycillin or clarithromycin for Helicobacter pylori eradication, in a region of high primary metronidazole resistance: the HERO study	Katelaris, P.; Adamthwaite, D.; Midolo, P.; Yeomans, N.; Davidson, G.; Lambert, J.
	2005	Enzyme replacement therapy for Gaucher disease in Australia	Goldblatt, J.; Szer, J.; Fletcher, J.; McGill, J.; Rowell, J.; Wilson, M.
	2007	A cross-sectional survey to assess community attitudes to introduction of human papillomavirus vaccine	Marshall, H.; Ryan, P.; Roberton, D.; Baghurst, P.
	2007	Promoting lay participation in medical school curriculum development: Lay and faculty perspectives	O'Keefe, M.; Jones, A.
	2005	The Hunter-McAlpine syndrome results from duplication 5q35-qter	Hunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
	2012	Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): A new autosomal dominant syndrome	Worthley, D.; Phillips, K.; Wayte, N.; Schrader, K.; Healey, S.; Kaurah, P.; Shulkes, A.; Grimpen, F.; Clouston, A.; Moore, D.; Cullen, D.; Ormonde, D.; Mounkley, D.; Wen, X.; Lindor, N.; Carniero, F.; Huntsman, D.; Chenevix-Trench, G.; Suthers, G.
	2010	Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registry	Walsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
	2005	Antro-pyloro-duodenal motor responses to gastric and duodenal nutrient in critically ill patients	Chapman, M.; Fraser, R.; Yandell, R.; Bryant, L.; Tam, W.; Nguyen, Q.; Zacharakis, B.; Butler, R.; Davidson, G.; Horowitz, M.
	2009	SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype	Spurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.