1. Adelaide Research & Scholarship

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Results 61-70 of 262 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2010A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
2010A new species of Neoheterocotyle Hargis, 1955 (Monogenea: Monocotylidae) from the gills of Rhinobatos annulatus Müller & Henle (Rhinobatidae) off the southern tip of AfricaVaughan, D.; Chisholm, L.
2010Cryogenic burns from intentional use of aerosol spray in children: An emerging phenomenonStefanutti, G.; Yee, J.; Sparnon, A.
2010Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephalyGiannandrea, M.; Bianchi, V.; Mignogna, M.; Sirri, A.; Carrabino, S.; D'Elia, E.; Vecellio, M.; Russo, S.; Cogliati, F.; Larizza, L.; Ropers, H.; Tzschach, A.; Kalscheuer, V.; Oehl-Jaschkowitz, B.; Skinner, C.; Schwartz, C.; Gecz, J.; Van Esch, H.; Raynaud, M.; Chelly, J.; et al.
2010Mitochondrial uncoupler FCCP activates proton conductance but does not block store-operated Ca2+ current in liver cellsTo, M.; Aromataris, E.; Castro, J.; Roberts, M.; Barritt, G.; Rychkov, G.
2010Reintervention after Mobile-bearing Oxford Unicompartmental Knee ArthroplastyClark, M.; Campbell, D.; Kiss, G.; Dobson, P.; Lewis, P.
2010The lacrimal bypass tube for lacrimal pump failure attributable to facial palsyMadge, S.; Malhotra, R.; deSousa, J.; McNab, A.; O'Donnell, B.; Dolman, P.; Selva-Nayagam, D.
2010Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndromeGecz, J.
2010Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determinationPearlman, A.; Loke, J.; Le Caignec, C.; White, S.; Chin, L.; Friedman, A.; Warr, N.; Willan, J.; Brauer, D.; Farmer, C.; Brooks, E.; Oddoux, C.; Riley, B.; Shajahan, S.; Camerino, G.; Homfray, T.; Crosby, A.; Couper, J.; David, A.; Greenfield, A.; et al.
2010Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceTischfield, M.; Baris, H.; Wu, C.; Rudolph, G.; van Maldergem, L.; He, W.; Chan, W.; Andrews, C.; Demer, J.; Robertson, R.; Mackey, D.; Ruddle, J.; Bird, T.; Gottlob, I.; Pieh, C.; Traboulsi, E.; Pomeroy, S.; Hunter, D.; Soul, J.; Newlin, A.; et al.

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