Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy von BERKOVIC, S. F, KNOWLTON, R. C, LEROY, R. F, SCHIEMANN, J, FALTER, U

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Clinical spectrum of early-onset epileptic: encephalopathies associated with STXBP1 mutations von DEPREZ, L, WECKHUYSEN, S, JORDANOVA, A, VAN COSTER, R, YENDLE, S, BERKOVIC, S. F, SCHEFFER, I, CEULEMANS, B, DE JONGHE, P, HOLMGREN, P, SULS, A, VAN DYCK, T, GOOSSENS, D, DEL-FAVERO, J, JANSEN, A, VERHAERT, K, LAGAE, L

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The core network in absence epilepsy: Differences in cortical and thalamic BOLD response von CARNEY, P. W, MASTERTON, R. A. J, HARVEY, A. S, SCHEFFER, I. E, BERKOVIC, S. F, JACKSON, G. D

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Seizure Outcome after Temporal Lobectomy: Current Research Practice and Findings von McIntosh, A. M., Wilson, S. J., Berkovic, S. F.

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The frontal lobe in absence epilepsy EEG-fMRI findings von CARNEY, P. W, MASTERTON, R. A. J, FLANAGAN, D, BERKOVIC, S. F, JACKSON, G. D

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Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy von TAN, N. C. K, HERON, S. E, SCHEFFER, I. E, PELEKANOS, J. T, MCMAHON, J. M, VEARS, D. F, MULLEY, J. C, BERKOVIC, S. F

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Severe myoclonic epilepsy of infancy (Dravet syndrome) : Recognition and diagnosis in adults von JANSEN, F. E, SADLEIR, L. G, HARKIN, L. A, VADLAMUDI, L, MCMAHON, J. M, MULLEY, J. C, SCHEFFER, I. E, BERKOVIC, S. F

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The management of epilepsy in pregnancy von Walker, SP, Permezel, M, Berkovic, SF

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How Mutations in the nAChRs Can Cause ADNFLE Epilepsy von Bertrand, D., Picard, F., Le Hellard, S., Weiland, S., Favre, I., Phillips, H., Bertrand, S., Berkovic, S. F., Malafosse, A., Mulley, J.

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A Potassium Channel Mutation in Neonatal Human Epilepsy von Biervert, Christian, Schroeder, Björn C., Kubisch, Christian, Berkovic, Samuel F., Propping, Peter, Jentsch, Thomas J., Steinlein, Ortrud K.

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SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure von Dibbens, L.M., Michelucci, R., Gambardella, A., Andermann, F., Rubboli, G., Bayly, M.A., Joensuu, T., Vears, D.F., Franceschetti, S., Canafoglia, L., Wallace, R., Bassuk, A.G., Power, D.A., Tassinari, C.A., Andermann, E., Lehesjoki, A.E., Berkovic, S.F.

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Sleep deprivation increases cortical excitability in epilepsy : Syndrome-specific effects von BADAWY, R. A. B, CURATOLO, J. M, NEWTON, M, BERKOVIC, S. F, MACDONELL, R. A. L

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Why do seizures in generalized epilepsy often occur in the morning? von BADAWY, R. A. B, MACDONELL, R. A. L, JACKSON, G. D, BERKOVIC, S. F

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New-onset temporal lobe epilepsy in children : Lesion on MRI predicts poor seizure outcome von SPOONER, C. G, BERKOVIC, S. F, MITCHELL, L. A, WRENNALL, J. A, HARVEY, A. S

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Severe Myoclonic Epilepsy of Infancy: Extended Spectrum of GEFS+? von Singh, R., Andermann, E., Whitehouse, W. P. A., Harvey, A. S., Keene, D. L., Seni, M‐H., Crossland, K. M., Andermann, F., Berkovic, S. F., Scheffer, I. E.

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A new molecular mechanism for severe myoclonic epilepsy of infancy : Exonic deletions in SCN1A von MULLEY, J. C, NELSON, P, SCHEFFER, I. E, GUERRERO, S, DIBBENS, L, IONA, X, MCMAHON, J. M, HARKIN, L, SCHOUTEN, J, YU, S, BERKOVIC, S. F

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Generalized epilepsy in hypothalamic hamartoma: Evolution and postoperative resolution von FREEMAN, J. L, HARVEY, A. S, ROSENFELD, J. V, WRENNALL, J. A, BAILEY, C. A, BERKOVIC, S. F

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Generalized epilepsy with febrile seizures plus: A genetic disorder with heterogeneous clinical phenotypes von SCHEFFER, I. E, BERKOVIC, S. F

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Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures von Heron, S E, Cox, K, Grinton, B E, Zuberi, S M, Kivity, S, Afawi, Z, Straussberg, R, Berkovic, S F, Scheffer, I E, Mulley, J C

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Reduced striatal D1 receptor binding in autosomal dominant nocturnal frontal lobe epilepsy von FEDI, M, BERKOVIC, S. F, SCHEFFER, I. E, O'KEEFE, G, MARINI, C, MULLIGAN, R, GONG, S, TOCHON-DANGUY, H, REUTENS, D. C

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