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 1-10 of 11 (Search time: 0.001 seconds).

previous
1
2
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2002	Alterations in corticospinal excitability with imposed vs. voluntary fatigue in human hand muscles	Pitcher, J.; Miles, T.
	2002	A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype	Cundy, T.; Hegde, M.; Naot, D.; Chong, B.; King, A.; Wallace, R.; Mulley, J.; Love, D.; Seidel, J.; Fawkner, M.; Banovic, T.; Callon, K.; Grey, A.; Reid, I.; Middleton-Hardie, C.; Cornish, J.
	2002	Sodium-channel defects in benign familial neonatal-infantile seizures	Heron, S.; Crossland, K.; Andermann, E.; Phillips, H.; Hall, A.; Bleasel, A.; Shevell, M.; Mercho, S.; Seni, M.; Guiot, M.; Mulley, J.; Berkovic, S.; Scheffer, I.
	2002	Long-term facilitation of ventilation is not present during wakefulness in healthy men or women	Jordan, A.; Catcheside, P.; O'Donoghue, F.; McEvoy, R.
	2002	Dexterity is not affected by fatigue-induced depression of human motor cortex excitability	Cole, J.; Ridding, M.; Miles, T.
	2002	Time course of induction of increased human motor cortex excitability by nerve stimulation	McKay, D.; Brooker, R.; Giacomin, P.; Ridding, M.; Miles, T.
	2002	Is birthweight a good marker for gestational exposures that increase the risk of adult disease?	Morley, R.; Owens, J.; Blair, E.; Dwyer, T.
	2002	X-linked myoclonic epilepsy with spasticity and intellectual disability - Mutation in the homeobox gene ARX	Scheffer, I.; Wallace, R.; Phillips, F.; Hewson, P.; Reardon, K.; Parasivam, G.; Stromme, P.; Berkovic, S.; Gecz, J.; Mulley, J.
	2002	Noninvasive cardiovascular markers of acoustically induced arousal from non-rapid-eye-movement sleep	Catcheside, P.; Orr, R.; Chiong, S.; Mercer, J.; Saunders, N.; McEvoy, R.
	2002	Correlation among genotype, phenotype, and biochemical markers in Gaucher disease: Implications for the prediction of disease severity	Whitfield, P.; Nelson, P.; Sharp, P.; Bindloss, C.; Dean, C.; Ravenscroft, E.; Fong, B.; Fietz, M.; Hopwood, J.; Meikle, P.