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Results 11-20 of 44 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2011Comparison of DNA extraction methods from small samples of newborn screening cards suitable for retrospective perinatal viral researchMcMichael, G.; Highet, A.; Gibson, C.; Goldwater, P.; O'Callaghan, M.; Alvino, E.; MacLennan, A.
2006Only an expert witness can prevent cerebral palsy!MacLennan, A.; Hankins, G.; Speer, M.
2002Who will deliver the next generation of Australians?MacLennan, A.; Spencer, M.
2006Cerebral palsy and the application of the international criteria for acute intrapartum hypoxiaStrijbis, E.; Oudman, I.; van Essen, P.; MacLennan, A.
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.
2013Cesarean delivery and cerebral palsy: A systematic review and meta-analysisO'Callaghan, M.; MacLennan, A.
2009The genomic basis of cerebral palsy: A HuGE systematic literature reviewO'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G.
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.
2013Genetic and clinical contributions to cerebral palsy: A multi-variable analysisO'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Baghurst, P.; Goldwater, P.; Dekker, G.
2013NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyMcMichael, G.; Haan, E.; Gardner, A.; Yap, T.; Thompson, S.; Ouvrier, R.; Dale, R.; Gecz, J.; MacLennan, A.

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