Adelaide Research & Scholarship
Browsing "School of Paediatrics & Reproductive Health" by Author Vadlamudi, L.
Showing results 1 to 5 of 5
| Preview | Issue Date | Title | Author(s) |
| 2008 | Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis | Berkovic, S.; Dibbens, L.; Oshlack, A.; Silver, J.; Katerelos, M.; Vears, D.; Lullmann-Rauch, R.; Blanz, J.; Zhang, K.; Stankovich, J.; Kalnins, R.; Dowling, J.; Andermann, E.; Andermann, F.; Faldini, E.; D'Hooge, R.; Vadlamudi, L.; Macdonnell, R.; Hodgson, B.; Bayly, M.; et al. |
| 2008 | Gene expression analysis in absence epilepsy using a monozygotic twin design | Helbig, I.; Matigian, N.; Vadlamudi, L.; Lawrence, K.; Bayly, M.; Bain, S.; Diyagama, D.; Scheffer, I.; Mulley, J.; Holloway, A.; Berkovic, S.; Hayward, N. |
| 2014 | Genetics of epilepsy: the testimony of twins in the molecular era | Vadlamudi, L.; Milne, R.; Lawrence, K.; Heron, S.; Eckhaus, J.; Keay, D.; Connellan, M.; Torn-Broers, Y.; Howell, R.; Mulley, J.; Scheffer, I.; Dibbens, L.; Hopper, J.; Berkovic, S. |
| 2014 | Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations | Scheffer, I.; Heron, S.; Regan, B.; Mandelstam, S.; Crompton, D.; Hodgson, B.; Licchetta, L.; Provini, F.; Bisulli, F.; Vadlamudi, L.; Gecz, J.; Connelly, A.; Tinuper, P.; Ricos, M.; Berkovic, S.; Dibbens, L. |
| 2010 | Timing of de novo mutagenesis - A twin study of sodium-channel mutations | Vadlamudi, L.; Dibbens, L.; Lawrence, K.; Iona, X.; McMahon, J.; Murrell, W.; Mackay-Sim, A.; Scheffer, I.; Berkovic, S. |
