-
Howell, KB, Freeman, JL, Mackay, MT, Fahey, MC, Archer, J, Berkovic, SF, Chan, E, Dabscheck, G, Eggers, S, Hayman, M, et al.
The severe epilepsy syndromes of infancy: A population-based study..
Epilepsia
62(2)
:
358 -370
2021
view publication
-
Macdonald-Laurs, E, Bailey, CA, Barton, S, Yang, JY-M, Mandelstam, S, Macgregor, D, Lockhart, PJ, Leventer, RJ, Maixner, WJ, Harvey, AS.
Clinical seizure manifestations in the absence of synaptic connections..
Epileptic Disord
23(1)
:
167 -172
2021
view publication
-
Eratne, D, Schneider, A, Lynch, E, Martyn, M, Velakoulis, D, Fahey, M, Kwan, P, Leventer, R, Rafehi, H, Chong, B, et al.
The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective..
J Neurol Sci
420:
117260
2021
view publication
-
Siffredi, V, Preti, MG, Kebets, V, Obertino, S, Leventer, RJ, McIlroy, A, Wood, AG, Anderson, V, Spencer-Smith, MM, Van De Ville, D.
Structural Neuroplastic Responses Preserve Functional Connectivity and Neurobehavioural Outcomes in Children Born Without Corpus Callosum..
Cereb Cortex
31(2)
:
1227 -1239
2021
view publication
-
Brock, S, Vanderhasselt, T, Vermaning, S, Keymolen, K, Régal, L, Romaniello, R, Wieczorek, D, Storm, TM, Schaeferhoff, K, Hehr, U, et al.
Defining the phenotypical spectrum associated with variants in TUBB2A..
J Med Genet
58(1)
:
33 -40
2021
view publication