Clinical utility of EEG in diagnosing and monitoring epilepsy in adults von Tatum, W.O., Rubboli, G., Kaplan, P.W., Mirsatari, S.M., Radhakrishnan, K., Gloss, D., Caboclo, L.O., Drislane, F.W., Koutroumanidis, M., Schomer, D.L., Kasteleijn-Nolst Trenite, D., Cook, Mark, Beniczky, S.

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Are adverse effects of antiepileptic drugs different in symptomatic partial and idiopathic generalized epilepsies? The Portuguese–Brazilian validation of the Liverpool Adverse Even... von Martins, H.H, Alonso, N.B, Vidal-Dourado, M, Carbonel, T.D, de Araújo Filho, G.M, Caboclo, L.O, Yacubian, E.M, Guilhoto, L.M

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Nonconvulsive status epilepticus in epileptic encephalopathies in childhood von Hamad, A.P., Ferrari-Marinho, T., Caboclo, L.O., Thomé, U., Fernandes, R.M.F.

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Balloon cells associated with granule cell dispersion in the dentate gyrus in hippocampal sclerosis von Thom, M., Martinian, L., Caboclo, L. O., McEvoy, A. W., Sisodiya, S. M.

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Corrigendum to “Clinical utility of EEG in diagnosing and monitoring epilepsy in adults” [Clin. Neurophysiol. 129 (2018) 1056–1082] von Tatum, W.O., Rubboli, G., Kaplan, P.W., Mirsattari, S.M., Radhakrishnan, K., Gloss, D., Caboclo, L.O., Drislane, F.W., Koutroumanidis, M., Schomer, D.L., Kasteleijn-Nolst Trenite, D., Cook, Mark, Beniczky, S.

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Response: Filamin A, Periventricular Nodular Heterotopia, and West Syndrome von Masruha, M.R., Caboclo, L.O., Carrete, H., Cendes, I.L., Rodrigues, M.G., Garzon, E., Yacubian, E.M., Sakamoto, A.C., Sheen, V., Harney, M., Neal, J., Hill, R., Bodell, A., Walsh, C., Vilanova, L.C.

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Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study von Kasperaviciūte, D, Catarino, C B, Heinzen, E L, Depondt, C, Cavalleri, G L, Caboclo, L O, Tate, S K, Jamnadas-Khoda, J, Chinthapalli, K, Clayton, L M S, Shianna, K V, Radtke, R A, Mikati, M A, Gallentine, W B, Husain, A M, Alhusaini, S, Leppert, D, Middleton, L T, Gibson, R A, Johnson, M R, Matthews, P M, Hosford, D, Heuser, K, Amos, L, Ortega, M, Zumsteg, D, Wieser, H G, Steinhoff, B J, Krämer, G, Hansen, J, Dorn, T, Kantanen, A M, Gjerstad, L, Peuralinna, T, Hernandez, D G, Eriksson, K J, Kälviäinen, R K, Doherty, C P, Wood, N W, Pandolfo, M, Duncan, J S, Sander, J W, Delanty, N, Goldstein, D B, Sisodiya, S M

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Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes von Heinzen, E L, Radtke, R A, Urban, T J, Cavalleri, G L, Depondt, C, Need, A C, Walley, N M, Nicoletti, P, Ge, D, Catarino, C B, Duncan, J S, Kasperaviciūte, D, Tate, S K, Caboclo, L O, Sander, J W, Clayton, L, Linney, K N, Shianna, K V, Gumbs, C E, Smith, J, Cronin, K D, Maia, J M, Doherty, C P, Pandolfo, M, Leppert, D, Middleton, L T, Gibson, R A, Johnson, M R, Matthews, P M, Hosford, D, Kälviäinen, R, Eriksson, K, Kantanen, A M, Dorn, T, Hansen, J, Krämer, G, Steinhoff, B J, Wieser, H G, Zumsteg, D, Ortega, M, Wood, N W, Huxley-Jones, J, Mikati, M, Gallentine, W B, Husain, A M, Buckley, P G, Stallings, R L, Podgoreanu, M V, Delanty, N, Sisodiya, S M, Goldstein, D B

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Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study von Kasperaviciute, D, Catarino, CB, Heinzen, EL, Depondt, C, Cavalleri, GL, Caboclo, LO, Tate, SK, Jamnadas-Khoda, J, Chinthapalli, K, Clayton, LMS, Shianna, KV, Radtke, RA, Mikati, MA, Gallentine, WB, Husain, AM, Alhusaini, S, Leppert, D, Middleton, LT, Gibson, RA, Johnson, MR, Matthews, PM, Hosford, D, Heuser, K, Amos, L, Ortega, M, Zumsteg, D, Wieser, H-G, Steinhoff, BJ, Kraermer, G, Hansen, J, Dorn, T, Kantanen, A-M, Gjerstad, L, Peuralinna, T, Hernandez, DG, Eriksson, KJ, Kalviainen, RK, Doherty, CP, Wood, NW, Pandolfo, M, Duncan, JS, Sander, JW, Delanty, N, Goldstein, DB, Sisodiya, SM

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Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes von Heinzen, EL, Radtke, RA, Urban, TJ, Cavalleri, GL, Depondt, C, Need, AC, Walley, NM, Nicoletti, P, Ge, DL, Catarino, CB, Duncan, JS, Kasperaviciute, D, Tate, SK, Caboclo, LO, Sander, JW, Clayton, L, Linney, KN, Shianna, KV, Gumbs, CE, Smith, J, Cronin, KD, Maia, JM, Doherty, CP, Pandolfo, M, Leppert, D, Middleton, LT, Gibson, RA, Johnson, MR, Matthews, PM, Hosford, D, Kalviainen, R, Eriksson, K, Kantanen, AM, Dorn, T, Hansen, J, Kramer, G, Steinhoff, BJ, Wieser, HG, Zumsteg, D, Ortega, M, Wood, NW, Huxley-Jones, J, Mikati, M, Gallentine, WB, Husain, AM, Buckley, PG, Stallings, RL, Podgoreanu, MV, Delanty, N, Sisodiya, SM, Goldstein, DB

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Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes von Heinzen, Erin L., Radtke, Rodney A., Urban, Thomas J., Cavalleri, Gianpiero L., Depondt, Chantal, Need, Anna C., Walley, Nicole M., Nicoletti, Paola, Ge, Dongliang, Catarino, Claudia B., Duncan, John S., Kasperavičiūte˙, Dalia, Tate, Sarah K., Caboclo, Luis O., Sander, Josemir W., Clayton, Lisa, Linney, Kristen N., Shianna, Kevin V., Gumbs, Curtis E., Smith, Jason, Cronin, Kenneth D., Maia, Jessica M., Doherty, Colin P., Pandolfo, Massimo, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Kälviäinen, Reetta, Eriksson, Kai, Kantanen, Anne-Mari, Dorn, Thomas, Hansen, Jörg, Krämer, Günter, Steinhoff, Bernhard J., Wieser, Heinz-Gregor, Zumsteg, Dominik, Ortega, Marcos, Wood, Nicholas W., Huxley-Jones, Julie, Mikati, Mohamad, Gallentine, William B., Husain, Aatif M., Buckley, Patrick G., Stallings, Ray L., Podgoreanu, Mihai V., Delanty, Norman, Sisodiya, Sanjay M., Goldstein, David B.

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Mutation in Filamin A Causes Periventricular Heterotopia, Developmental Regression, and West Syndrome in Males von Masruha, Marcelo R., Caboclo, Luis O. S. F., Carrete, Henrique, Cendes, Íscia L., Rodrigues, Murilo G., Garzon, Eliana, Yacubian, Elza M. T., Sakamoto, Américo C., Sheen, Volney, Harney, Megan, Neal, Jason, Sean Hill, R., Bodell, Adria, Walsh, Christopher, Vilanova, Luiz C. P.

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Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study von Kasperavičiūtė, Dalia, Catarino, Claudia B., Heinzen, Erin L., Depondt, Chantal, Cavalleri, Gianpiero L., Caboclo, Luis O., Tate, Sarah K., Jamnadas-Khoda, Jenny, Chinthapalli, Krishna, Clayton, Lisa M.S., Shianna, Kevin V., Radtke, Rodney A., Mikati, Mohamad A., Gallentine, William B., Husain, Aatif M., Alhusaini, Saud, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Heuser, Kjell, Amos, Leslie, Ortega, Marcos, Zumsteg, Dominik, Wieser, Heinz-Gregor, Steinhoff, Bernhard J., Krämer, Günter, Hansen, Jörg, Dorn, Thomas, Kantanen, Anne-Mari, Gjerstad, Leif, Peuralinna, Terhi, Hernandez, Dena G., Eriksson, Kai J., Kälviäinen, Reetta K., Doherty, Colin P., Wood, Nicholas W., Pandolfo, Massimo, Duncan, John S., Sander, Josemir W., Delanty, Norman, Goldstein, David B., Sisodiya, Sanjay M.

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Can intraoperative electrocorticography patterns predict surgical outcome in patients with temporal lobe epilepsy secondary to unilateral mesial temporal sclerosis? von Oliveira, Pedro A.L., Garzon, Eliana, Caboclo, Luís O.S.F., Sousa, Patrícia S., Carrete, Henrique, Centeno, Ricardo S., Costa, José M.P., Machado, Hélio R., Yacubian, Elza M.T., Bianchin, Marino M., Sakamoto, Américo C.

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Alterações microestruturais e físicas em filmes de CdS submetidos a tratamento térmico em presença de CdCl2 von Caboclo, G. D., Fernandes, J. A. S., Pinheiro, W. A., Cruz, L. R.

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