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PreviewIssue DateTitleAuthor(s)
1997A dose-intensive, cyclophosphamide-based regimen for the treatment of recurrent/progressive or advanced solid tumors of childhood: a report from the Australia and New Zealand Children's Cancer Study GroupCarpenter, P.; White, L.; McCowage, G.; Nayanar, V.; Toogood, I.; Shaw, P.; Lockwood, L.; Tiedemann, K.
2011A guide to using Team Management Systems (TMS) for learning and teaching quality improvement in health care teamsO'Keefe, M.F.; McAllister, S.; Burgess, T.; Stupans, I.; LeCouteur, A.; Australian Learning and Teaching Council
2011A high-throughput platform for lentiviral overexpression screening of the human ORFeomeSkalamera, D.; Ranall, M.; Wilson, B.; Leo, P.; Purdon, A.; Hyde, C.; Nourbakhsh, E.; Grimmond, S.; Barry, S.; Gabrielli, B.; Gonda, T.; Jothi, R.
2011A lipidomic screen of palmitate-treated MIN6 β-cells links sphingolipid metabolites with endoplasmic reticulum (ER) stress and impaired protein traffickingBoslem, E.; Macintosh, G.; Preston, A.; Bartley, C.; Busch, A.; Fuller, M.; Laybutt, D.; Meikle, P.; Biden, T.
2013A long-term evaluation of 150 costochondral nasal graftsChummun, S.; McLean, N.; Anderson, P.; David, D.
1997A membrane protein primarily associated with the lysosomal compartmentBrooks, D.; Bradford, T.; Carlsson, S.; Hopwood, J.
2011A method to objectively assess swallow function in adults with suspected aspirationOmari, T.; Dejaeger, E.; Van Beckevoort, D.; Goeleven, A.; Davidson, G.; Dent, J.; Tack, J.; Rommel, N.
1999A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardationMerienne, K.; Jacquot, S.; Pannetier, S.; Zeniou, M.; Bankier, A.; Gecz, J.; Mandel, J.L.; Mulley, J.; Sassone-Corsi, P.; Hanauer, A.
1995A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsySteinlein, O.; Mulley, J.; Propping, P.; Wallace, R.; Phillips, H.; Sutherland, G.; Scheffer, I.; Berkovic, S.
2012A model of care for familial hypercholesterolaemia: key role for clinical biochemistryWatts, G.; Sullivan, D.; van Bockxmeer, F.; Poplawski, N.; Hamilton-Craig, I.; Clifton, P.; O'Brien, R.; George, P.; Burnett, J.
2007A mouse model for assessing the impact of ingested nutrients on gastric emptying rateSymonds, E.; Butler, R.; Omari, T.
1999A mouse model for mucopolysaccharidosis type III A (Sanfilippo syndrome)Bhaumik, M.; Muller, V.; Rozaklis, T.; Johnson, L.; Dobrenis, K.; Bhattacharyya, R.; Wurzelmann, S.; Finamore, P.; Hopwood, J.; Walkley, S.; Stanley, P.
2008A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritisMartin, D.; Atmuri, V.; Hemming, R.; Farley, J.; Mort, J.; Byers, S.; Hombach-Klonisch, S.; Stern, R.; Triggs-Raine, B.
2021A multi-centre, open label, randomised, parallel-group, superiority Trial to compare the efficacy of URsodeoxycholic acid with RIFampicin in the management of women with severe early onset Intrahepatic Cholestasis of pregnancy: the TURRIFIC randomised trialHague, W.M.; Callaway, L.; Chambers, J.; Chappell, L.; Coat, S.; de Haan-Jebbink, J.; Dekker, M.; Dixon, P.; Dodd, J.; Fuller, M.; Gordijn, S.; Graham, D.; Heikinheimo, O.; Hennessy, A.; Kaaja, R.; Khong, T.Y.; Lampio, L.; Louise, J.; Makris, A.; Markus, C.; et al.
2017A multicentre randomised controlled trial of levetiracetam versus phenytoin for convulsive status epilepticus in children (protocol): Convulsive Status Epilepticus Paediatric Trial (ConSEPT) - a PREDICT studyDalziel, S.R.; Furyk, J.; Bonisch, M.; Oakley, E.; Borland, M.; Neutze, J.; Donath, S.; Sharpe, C.; Harvey, S.; Davidson, A.; Craig, S.; Phillips, N.; George, S.; Rao, A.; Cheng, N.; Zhang, M.; Sinn, K.; Kochar, A.; Brabyn, C.; Babl, F.E.
1995A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyLaing, N.; Wilton, S.; Akkari, P.; Dorosz, S.; Boundy, K.; Kneebone, C.; Blumbergs, P.; White, S.; Watkins, H.; Love, D.; Haan, E.
2012A new model of care for familial hypercholesterolaemia: What is the role of cardiology?Watts, G.; Sullivan, D.; van Bockxmeer, F.; Poplawski, N.; Hamilton-Craig, I.; Clifton, P.; O'Brien, R.; Bishop, W.; George, P.; Semsarian, C.; Tonkin, A.
2011A new syndrome with craniosynostosis and cleft lip and palateAnderson, P.; Haan, E.; David, D.
2010A new technique to examine individual pollutant particle and fibre deposition and transit behaviour in live mouse tracheaDonnelley, M.; Siu, K.; Morgan, K.; Skinner, W.; Suzuki, Y.; Takeuchi, A.; Uesugi, K.; Yagi, N.; Parsons, D.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.