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 11-20 of 80 (Search time: 0.003 seconds).

previous
1
2
3
4
5
...
8
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2019	GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon	Tingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
	1999	Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda	Gedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
	2013	Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and function to evade naturally acquired immunity	Persson, K.; Fowkes, F.; McCallum, F.; Gicheru, N.; Reiling, L.; Richards, J.; Wilson, D.; Lopaticki, S.; Cowman, A.; Marsh, K.; Beeson, J.
	2001	Improvement in intestinal permeability precedes morphometric recovery of the small intestine in coeliac disease	Cummins, A.; Thompson, F.; Butler, R.; Cassidy, J.; Gillis, D.; Lorenzetti, M.; Southcott, E.; Wilson, P.
	2023	The effects of age and biological sex on the association between I-wave recruitment and the response to cTBS: an exploratory study	Van Dam, J.M.; Graetz, L.; Pitcher, J.B.; Goldsworthy, M.R.
	2009	Long-term effects of a very low-carbohydrate diet and a low-fat diet on mood and cognitive function	Brinkworth, G.; Buckley, J.; Noakes, M.; Clifton, P.; Wilson, C.
	2013	Axl mediates acquired resistance of head and neck cancer cells to the epidermal growth factor receptor inhibitor erlotinib	Giles, K.; Kalinowski, F.; Candy, P.; Epis, M.; Zhang, P.; Redfern, A.; Stuart, L.; Goodall, G.; Leedman, P.
	2004	Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy	Berkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
	2013	Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features	Bonnefond, A.; Raimondo, A.; Stutzmann, F.; Ghoussaini, M.; Ramachandrappa, S.; Bersten, D.; Durand, E.; Vatin, V.; Balkau, B.; Lantieri, O.; Raverdy, V.; Pattou, F.; Van Hul, W.; Van Gaal, L.; Peet, D.; Weill, J.; Miller, J.; Horber, F.; Goldstone, A.; Driscoll, D.; et al.
	2003	X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3	Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J.