Showing results 31 to 46 of 46
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Preview | Issue Date | Title | Author(s) |
| 2006 | Neurotropic viruses and cerebral palsy: population based case-control study | Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G. |
| 2013 | NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy | McMichael, G.; Haan, E.; Gardner, A.; Yap, T.; Thompson, S.; Ouvrier, R.; Dale, R.; Gecz, J.; MacLennan, A. |
| 2006 | Obstetric litigation is asphyxiating our maternity services | Hankins, G.; MacLennan, A.; Speer, M.; Strunk, A.; Nelson, K. |
| 2006 | Only an expert witness can prevent cerebral palsy! | MacLennan, A.; Hankins, G.; Speer, M. |
| 2013 | Rare copy number variation in cerebral palsy | McMichael, 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. |
| 2000 | Risk management in cerebral palsy | MacLennan, A. |
| 2013 | Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysis | O'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; Dekker, G. |
| 2008 | The antenatal causes of cerebral palsy - Genetic and viral associations | Gibson, C.; MacLennan, A.; Goldwater, P.; Dekker, G. |
| 2006 | The association between inherited cytokine polymorphisms and cerebral palsy | Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; Hague, W.; Morton, M. |
| 2011 | The Australian cerebral palsy research study - Protocol for a national collaborative study investigating genomic and clinical associations with cerebral palsy | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Priest, K.; Goldwater, P.; Dekker, G. |
| 2009 | The genomic basis of cerebral palsy: A HuGE systematic literature review | O'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G. |
| 1995 | The origins of cerebral palsy - A consensus statement | MacLennan, 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. |
| 2005 | The prevalence of inherited thrombophilias in a Caucasian Australian population | Gibson, C.; MacLennan, A.; Rudzki, Z.; Hague, W.; Haan, E.; Sharpe, P.; Priest, K.; Chan, A.; Dekker, G.; Khong, T. |
| 2005 | Who will deliver our grandchildren? Implications of cerebral palsy litigation | MacLennan, A.; Nelson, K.; Hankins, G.; Speer, M. |
| 2002 | Who will deliver the next generation of Australians? | MacLennan, A.; Spencer, M. |
| 2013 | ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity | Hirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J. |