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Results 1-10 of 39 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Hemispheric differences in motor cortex excitability during a simple index finger abduction task in humansSemmler, J.; Nordstrom, M.
2003Control of human mandibular posture during locomotionMiles, T.; Flavel, S.; Nordstrom, M.
2002Alterations in corticospinal excitability with imposed vs. voluntary fatigue in human hand musclesPitcher, J.; Miles, T.
2002A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotypeCundy, 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.
2004Motor-unit coherence and its relation with synchrony are influenced by trainingSemmler, J.; Sale, M.; Meyer, F.; Nordstrom, M.
2005A community-based intervention to reduce antibiotic use for upper respiratory tract infections in regional South AustraliaDollman, W.; LeBlanc, V.; Stevens, L.; O'Connor, P.; Turnidge, J.
2017Expression patterns of HENMT1 and PIWIL1 in human testis: implications for transposon expressionHempfling, A.; Lim, S.; Adelson, D.; Evans, J.; O Connor, A.; Qu, Z.; Kliesch, S.; Weidner, W.; O Bryan, M.; Bergmann, M.
2019GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in CameroonTingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
1999Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaGedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
2017Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingJansen, I.E.; Ye, H.; Heetveld, S.; Lechler, M.C.; Michels, H.; Seinstra, R.I.; Lubbe, S.J.; Drouet, V.; Lesage, S.; Majounie, E.; Gibbs, J.R.; Nalls, M.A.; Ryten, M.; Botia, J.A.; Vandrovcova, J.; Simon-Sanchez, J.; Castillo-Lizardo, M.; Rizzu, P.; Blauwendraat, C.; Chouhan, A.K.; et al.