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Johannesen, KM, Gardella, E, Scheffer, I, Howell, K, Smith, DM, Helbig, I, Møller, RS, Rubboli, G.
Early mortality in SCN8A-related epilepsies.
Epilepsy Research
143:
79 -81
2018
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Berecki, G, Howell, KB, Deerasooriya, YH, Cilio, MR, Oliva, MK, Kaplan, D, Scheffer, IE, Berkovic, SF, Petrou, S.
Dynamic action potential clamp predicts functional separation in mild familial and severe de novo forms of SCN2A epilepsy.
Proceedings of the National Academy of Sciences of the United States of America
115(24)
:
e5516 -e5525
2018
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Howell, KB, Eggers, S, Dalziel, K, Riseley, J, Mandelstam, S, Myers, CT, McMahon, JM, Schneider, A, Carvill, GL, Mefford, HC, et al.
A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy.
Epilepsia
59(6)
:
1177 -1187
2018
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Manikkam, SA, Chetcuti, K, Howell, KB, Savarirayan, R, Fink, AM, Mandelstam, SA.
Temporal Lobe Malformations in Achondroplasia: Expanding the Brain Imaging Phenotype Associated with FGFR3-Related Skeletal Dysplasias.
American Journal of Neuroradiology
39(2)
:
380 -384
2018
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Corbett, MA, Bellows, ST, Li, M, Carroll, R, Micallef, S, Carvill, GL, Myers, CT, Howell, KB, Maljevic, S, Lerche, H, et al.
Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.
Neurology
87(19)
:
1975 -1984
2016
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