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Showing results 33 to 46 of 46 < previous 
PreviewIssue DateTitleAuthor(s)
2006Obstetric litigation is asphyxiating our maternity servicesHankins, G.; MacLennan, A.; Speer, M.; Strunk, A.; Nelson, K.
2006Only an expert witness can prevent cerebral palsy!MacLennan, A.; Hankins, G.; Speer, M.
2013Rare copy number variation in cerebral palsyMcMichael, G.; Girirajan, S.; Moreno-De-Luca, A.; Gecz, J.; Shard, C.; Nguyen, L.; Nicholl, J.; Gibson, C.; Haan, E.; Eichler, E.; Martin, C.; MacLennan, A.
2000Risk management in cerebral palsyMacLennan, A.
2013Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysisO'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; Dekker, G.
2008The antenatal causes of cerebral palsy - Genetic and viral associationsGibson, C.; MacLennan, A.; Goldwater, P.; Dekker, G.
2006The association between inherited cytokine polymorphisms and cerebral palsyGibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; Hague, W.; Morton, M.
2011The Australian cerebral palsy research study - Protocol for a national collaborative study investigating genomic and clinical associations with cerebral palsyO'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Priest, K.; Goldwater, P.; Dekker, G.
2009The genomic basis of cerebral palsy: A HuGE systematic literature reviewO'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G.
1995The origins of cerebral palsy - A consensus statementMacLennan, A.; Stanley, F.; Blair, E.; Rice, G.; Stone, P.; Robinson, J.; Henderson-Smart, D.; Yu, V.; Harbord, M.; Stern, L.; Chambers, H.; Furness, M.; Hayward, T.; Eckert, K.; Boundy, C.; Merrett, S.; Kenny, M.
2005The prevalence of inherited thrombophilias in a Caucasian Australian populationGibson, C.; MacLennan, A.; Rudzki, Z.; Hague, W.; Haan, E.; Sharpe, P.; Priest, K.; Chan, A.; Dekker, G.; Khong, T.
2005Who will deliver our grandchildren? Implications of cerebral palsy litigationMacLennan, A.; Nelson, K.; Hankins, G.; Speer, M.
2002Who will deliver the next generation of Australians?MacLennan, A.; Spencer, M.
2013ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
Showing results 33 to 46 of 46 < previous