Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3 von HEDERA, P, BLAIR, M. A, ABOU-KHALIL, B, ANDERMANN, E, ANDERMANN, F, D'AGOSTINO, D, TAYLOR, K. A, CHAHINE, L, PANDOLFO, M, BRADFORD, Y, HAINES, J. L

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Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures von NOACHTAR, S, ANDERMANN, E, MEYVISCH, P, ANDERMANN, F, GOUGH, W. B, SCHIEMANN-DELGADO, J

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Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis von Smith, Katherine R, Dahl, Hans-Henrik M, Canafoglia, Laura, Andermann, Eva, Damiano, John, Morbin, Michela, Bruni, Amalia C, Giaccone, Giorgio, Cossette, Patrick, Saftig, Paul, Grötzinger, Joachim, Schwake, Michael, Andermann, Frederick, Staropoli, John F, Sims, Katherine B, Mole, Sara E, Franceschetti, Silvana, Alexander, Noreen A, Cooper, Jonathan D, Chapman, Harold A, Carpenter, Stirling, Berkovic, Samuel F, Bahlo, Melanie

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Genetics of malformations of cortical development von Andermann, E

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Pathophysiological mechanisms of dominant and recessive GLRA1 mutations in hyperekplexia von Chung, Seo-Kyung, Vanbellinghen, Jean-François, Mullins, Jonathan G L, Robinson, Angela, Hantke, Janina, Hammond, Carrie L, Gilbert, Daniel F, Freilinger, Michael, Ryan, Monique, Kruer, Michael C, Masri, Amira, Gurses, Candan, Ferrie, Colin, Harvey, Kirsten, Shiang, Rita, Christodoulou, John, Andermann, Frederick, Andermann, Eva, Thomas, Rhys H, Harvey, Robert J, Lynch, Joseph W, Rees, Mark I

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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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A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population von Martin, C., Meloche, C., Rioux, M.-F., Nguyen, D.K., Carmant, L., Andermann, E., Gravel, M., Cossette, P.

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Intrinsic epileptogenicity in polymicrogyric cortex suggested by EEG-fMRI BOLD responses von KOBAYASHI, E, BAGSHAW, A. P, JANSEN, A, ANDERMANN, F, ANDERMANN, E, GOTMAN, J, DUBEAU, F

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Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease von Cadieux-Dion, M, Andermann, E, Lachance-Touchette, P, Ansorge, O, Meloche, C, Barnabé, A, Kuzniecky, RI, Andermann, F, Faught, E, Leonberg, S, Damiano, JA, Berkovic, SF, Rouleau, GA, Cossette, P

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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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1. Benign form of Unverricht–Lundborg disease (ULD) mimicking juvenile myoclonic epilepsy (JME) in adulthood von Amrom, D, Moghaddam, M.R. Heshmati, Andermann, F, Lehesjoki, A.-E, Andermann, E

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Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms von WALLACE, R. H, HODGSON, B. L, YAMAMOTO, T, ANDERMANN, E, MULLEY, J. C, BERKOVIC, S. F, SCHEFFER, I. E, GRINTON, B. E, GARDINER, R. M, ROBINSON, R, RODRIGUEZ-CASERO, V, SADLEIR, L, MORGAN, J, HARKIN, L. A, DIBBENS, L. M

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Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome von SHEEN, V. L, JANSEN, A, VAID, R. R, RUIZ, D. E, HUTCHINS, G. M, MENASHA, J, WILLNER, J, GENG, Y, GRIPP, K. W, NICHOLSON, L, BERRY-KRAVIS, E, BODELL, A, CHEN, M. H, APSE, K, HILL, R. S, DUBEAU, F, ANDERMANN, F, BARKOVICH, J, ANDERMANN, E, SHUGART, Y. Y, THOMAS, P, VIRI, M, VEGGIOTTI, P, PARRINI, E, ROBERTSON, S, GUERRINI, R, WALSH, C. A, MORGAN, T, RAVENSCROFT, R, GANESH, V, UNDERWOOD, T, WILEY, J, LEVENTER, R

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Congenital malformations due to antiepileptic drugs von Kaneko, S, Battino, D, Andermann, E, Wada, K, Kan, R, Takeda, A, Nakane, Y, Ogawa, Y, Avanzini, G, Fumarola, C, Granata, T, Molteni, F, Pardi, G, Minotti, L, Canger, R, Dansky, L, Oguni, M, Lopes-Cendas, I, Sherwin, A, Andermann, F, Seni, M.-H, Okada, M, Teranishi, T

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Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy von KOBAYASHI, E, D'AGOSTINO, M. D, LOPES-CENDES, I, BERKOVIC, S. F, LI, M. L, ANDERMANN, E, ANDERMANN, F, CENDES, F

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Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3 von Hedera, P, Blair, M A, Andermann, E, Andermann, F, D'Agostino, D, Taylor, K A, Chahine, L, Pandolfo, M, Bradford, Y, Haines, J L, Abou-Khalil, B

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Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24 von Phillips, H.A., Scheffer, I.E., Crossland, K.M., Bhatia, K.P., Fish, D.R., Marsden, C.D., Howell, S.J.L., Stephenson, J.B.P., Tolmie, J., Plazzi, G., Eeg-Olofsson, O., Singh, R., Lopes-Cendes, I., Andermann, E., Andermann, F., Berkovic, S.F., Mulley, J.C.

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Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment von Guerreiro, M. M., Andermann, E., Guerrini, R., Dobyns, W. B., Kuzniecky, R., Silver, K., Van Bogaert, P., Gillain, C., David, P., Ambrosetto, G., Rosati, A., Bartolomei, F., Parmeggiani, A., Paetau, R., Salonen, O., Ignatius, J., Borgatti, R., Zucca, C., Bastos, A. C., Palmini, A., Fernandes, W., Montenegro, M. A., Cendes, F., Andermann, F.

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Posterior quadrantic dysplasia or hemi-hemimegalencephaly: A characteristic brain malformation von D'AGOSTINO, M. D, BASTOS, A, CROSS, H, ANDERMANN, E, DUBEAU, F, MONTES, J, OLIVIER, A, ANDERMANN, F, PIRAS, C, BERNASCONI, A, GRISAR, T, GROSS TSUR, V, SNIPES, J, JUHASZ, C, CHUGANI, H, GUERRINI, R

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Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome von KOGAN, C. S, BERTONE, A, CORNISH, K, BOUTET, I, DER KALOUSTIAN, V. M, ANDERMANN, E, FAUBERT, J, CHAUDHURI, A

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