-
Ramanathan, S, Prelog, K, Barnes, EH, Tantsis, EM, Reddel, SW, Henderson, APD, Vucic, S, Gorman, MP, Benson, LA, Alper, G, et al.
Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis..
Mult Scler
22(4)
:
470 -482
2016
view publication
-
Nosadini, M, Alper, G, Riney, CJ, Benson, LA, Mohammad, SS, Ramanathan, S, Nolan, M, Appleton, R, Leventer, RJ, Deiva, K, et al.
Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder..
Neurol Neuroimmunol Neuroinflamm
3(1)
:
e188
2016
view publication
-
Sim, JC, Scerri, T, Fanjul-Fernández, M, Riseley, JR, Gillies, G, Pope, K, van Roozendaal, H, Heng, JI, Mandelstam, SA, McGillivray, G, et al.
Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3..
Ann Neurol
79(1)
:
132 -137
2016
view publication
-
Jansen, AC, Robitaille, Y, Honavar, M, Mullatti, N, Leventer, RJ, Andermann, E, Andermann, F, Squier, W.
The histopathology of polymicrogyria: a series of 71 brain autopsy studies..
Dev Med Child Neurol
58(1)
:
39 -48
2016
view publication
-
Damiano, JA, Afawi, Z, Bahlo, M, Mauermann, M, Misk, A, Arsov, T, Oliver, KL, Dahl, H-HM, Shearer, AE, Smith, RJH, et al.
Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia..
Hum Mol Genet
24(16)
:
4483 -4490
2015
view publication