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Results 11-20 of 107 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2019Anticipation of a midsession reversal in humansMcMillan, N.; Spetch, M.L.
2019"Anybody can make kids; it takes a real man to look after your kids": Aboriginal men's discourse on parentingCanuto, K.; Towers, K.; Riessen, J.; Perry, J.; Bond, S.; Ah Chee, D.; Brown, A.; Yousafzai, A.K.
2019Recessive DES cardio/myopathy without myofibrillar aggregates: intronic splice variant silences one allele leaving only missense L190P-desminRiley, L.G.; Waddell, L.B.; Ghaoui, R.; Evesson, F.J.; Cummings, B.B.; Bryen, S.J.; Joshi, H.; Wang, M.X.; Brammah, S.; Kritharides, L.; Corbett, A.; MacArthur, D.G.; Cooper, S.T.
2019A randomized controlled trial testing provision of fecal and blood test options on participation for colorectal cancer screeningSymonds, E.L.; Hughes, D.; Flight, I.; Woodman, R.; Chen, G.; Ratcliffe, J.; Pedersen, S.K.; Fraser, R.J.L.; Young, G.P.; Wilson, C.J.
2019'We're here to listen and help them as well': a qualitative study of staff and Indigenous patient perceptions about participating in social and emotional wellbeing research at primary healthcare servicesFarnbach, S.; Gee, G.; Eades, A.-M.; Evans, J.R.; Fernando, J.; Hammond, B.; Simms, M.; DeMasi, K.; Hackett, M.L.; Teixeira-Pinto, A.; Glozier, N.; Skinner, T.; Askew, D.; Cass, A.; Brown, A.
2019Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.
2019Association of HIV preexposure prophylaxis with incidence of sexually transmitted infections among individuals at high risk of HIV infectionTraeger, M.W.; Cornelisse, V.J.; Asselin, J.; Price, B.; Roth, N.J.; Willcox, J.; Tee, B.K.; Fairley, C.K.; Chang, C.C.; Armishaw, J.; Vujovic, O.; Penn, M.; Cundill, P.; Forgan-Smith, G.; Gall, J.; Pickett, C.; Lal, L.; Mak, A.; Spelman, T.D.; Long, N.; et al.
2019Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionGuo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
2019Getting it Right: validating a culturally specific screening tool for depression (aPHQ-9) in Aboriginal and Torres Strait Islander AustraliansHackett, M.L.; Teixeira-Pinto, A.; Farnbach, S.; Glozier, N.; Skinner, T.; Askew, D.A.; Gee, G.; Cass, A.; Brown, A.
2019Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant dataPatel, R.S.; Schmidt, A.F.; Tragante, V.; McCubrey, R.O.; Holmes, M.; Howe, L.J.; Direk, K.; Akerblom, A.; Leander, K.; Virani, S.S.; Kaminski, K.A.; Muehlschlegel, J.D.; Dube, M.-P.; Allayee, H.; Almgren, P.; Alver, M.; Baranova, E.; Behlouli, H.; Boeckx, B.; Braund, P.S.; et al.

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