Neuropathy in multiple myeloma treated with thalidomide : A prospective study von PLASMATI, R, PASTORELLI, F, MICHELUCCI, R, TASSINARI, C. A, CAVO, M, PETRACCI, E, ZAMAGNI, E, TOSI, P, CANGINI, D, TACCHETTI, P, SALVI, F, BARTOLOMEI, I

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Transcranial magnetic stimulation and epilepsy von Tassinari, Carlo Alberto, Cincotta, Massimo, Zaccara, Gaetano, Michelucci, Roberto

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Evaluation of two hydropower plants in Brazil: using emergy for exploring regional possibilities von Tassinari, C.A., Bonilla, S.H., Agostinho, F., Almeida, C.M.V.B., Giannetti, B.F.

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Impaired facial emotion recognition in early-onset right mesial temporal lobe epilepsy von MELETTI, S, BENUZZI, F, RUBBOLI, G, CANTALUPO, G, STANZANI MASERATI, M, NICHELLI, P, TASSINARI, C. A

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Central pattern generators for a common semiology in fronto-limbic seizures and in parasomnias. A neuroethologic approach von Tassinari, C A, Rubboli, G, Gardella, E, Cantalupo, G, Calandra-Buonaura, G, Vedovello, M, Alessandria, M, Gandini, G, Cinotti, S, Zamponi, N, Meletti, S

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Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia von Tassinari, C.A, Rubboli, G, Volpi, L, Meletti, S, d'Orsi, G, Franca, M, Sabetta, A.R, Riguzzi, P, Gardella, E, Zaniboni, A, Michelucci, R

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Lafora disease due to EPM2B mutations : A clinical and genetic study von GOMEZ-ABAD, C, GOMEZ-GARRE, P, GUTIERREZ-DELICADO, E, SAYGI, S, MICHELUCCI, R, TASSINARI, C. A, RODRIGUEZ DE CORDOBA, S, SERRATOSA, J. M

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Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases von Bisulli, F., Tinuper, P., Avoni, P., Striano, P., Striano, S., d’Orsi, G., Vignatelli, L., Bagattin, A., Scudellaro, E., Florindo, I., Nobile, C., Tassinari, C. A., Baruzzi, A., Michelucci, R.

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Rhythmic teeth grinding induced by temporal lobe seizures von MELETTI, S, CANTALUPO, G, VOLPI, L, RUBBOLI, G, MAGAUDDA, A, TASSINARI, C. A

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Epilepsy and EEG Findings in Males with Fragile X Syndrome von Musumeci, S. A., Hagerman, R. J., Ferri, R., Bosco, P., Bernardina, B. Dalla, Tassinari, C. A., Sarro, G. B., Elia, M.

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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy von Morante-Redolat, José M., Gorostidi-Pagola, Ana, Piquer-Sirerol, Salomé, Sáenz, Amets, Poza, Juan J., Galán, Juan, Gesk, Stefan, Sarafidou, Theologia, Mautner, Victor-F., Binelli, Simona, Staub, Eike, Hinzmann, Bernd, French, Lisa, Prud'homme, Jean-F., Passarelli, Daniela, Scannapieco, Paolo, Tassinari, Carlo A., Avanzini, Giuliano, Martí-Massó, José F., Kluwe, Lan, Deloukas, Panagiotis, Moschonas, Nicholas K., Michelucci, Roberto, Siebert, Reiner, Nobile, Carlo, Pérez-Tur, Jordi, López de Munain, Adolfo

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Clinical features and long term outcome of epilepsy in periventricular nodular heterotopia. Simple compared with plus forms von d’Orsi, G, Tinuper, P, Bisulli, F, Zaniboni, A, Bernardi, B, Rubboli, G, Riva, R, Michelucci, R, Volpi, L, Tassinari, C A, Baruzzi, A

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Effects of chronic levodopa and pergolide treatment on cortical excitability in patients with Parkinson's disease: a transcranial magnetic stimulation study von Strafella, A.P, Valzania, F, Nassetti, S.A, Tropeani, A, Bisulli, A, Santangelo, M, Tassinari, C.A

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Suppressive Efficacy by a Commercially Available Blue Lens on PPR in 610 Photosensitive Epilepsy Patients von Capovilla, Giuseppe, Gambardella, Antonio, Rubboli, Guido, Beccaria, Francesca, Montagnini, Alessandra, Aguglia, Umberto, Canevini, Maria Paola, Casellato, Susanna, Granata, Tiziana, Paladin, Francesco, Romeo, Antonino, Stranci, Giuseppe, Tinuper, Paolo, Veggiotti, Pierangelo, Avanzini, Giuliano, Tassinari, Carlo Alberto

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Subcortical Band Heterotopia in Rare Affected Males Can be Caused by Missense Mutations in DCX (XLIS) or LIS1 von Pilz, Daniela T., Kuc, Julie, Matsumoto, Naomichi, Bodurtha, Joann, Bernadi, Bruno, Tassinari, Carlo A., Dobyns, William B., Ledbetter, David H.

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Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families von Michelucci, Roberto, Poza, Juan Jose, Sofia, Vito, Feo, Maria Rita de, Binelli, Simona, Bisulli, Francesca, Scudellaro, Evan, Simionati, Barbara, Zimbello, Rosanna, D'Orsi, Giuseppe, Passarelli, Daniela, Avoni, Patrizia, Avanzini, Giuliano, Tinuper, Paolo, Biondi, Roberto, Valle, Giorgio, Mautner, Victor F., Stephani, Ulrich, Tassinari, Carlo Alberto, Moschonas, Nicholas K., Siebert, Reiner, Munain, Adolpho Lopez de, Perez‐Tur, Jordi, Nobile, Carlo

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Impaired fear processing in right mesial temporal sclerosis: a fMRI study von Benuzzi, Francesca, Meletti, Stefano, Zamboni, Giovanna, Calandra-Buonaura, Giovanna, Serafini, Marco, Lui, Fausta, Baraldi, Patrizia, Rubboli, Guido, Tassinari, Carlo Alberto, Nichelli, Paolo

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Negative myoclonus induced by cortical electrical stimulation in epileptic patients von Rubboli, Guido, Mai, Roberto, Meletti, Stefano, Francione, Stefano, Cardinale, Francesco, Tassi, Laura, Russo, Giorgio Lo, Stanzani-Maserati, Michelangelo, Cantalupo, Gaetano, Tassinari, Carlo Alberto

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Epilepsy with Myoclonic absences von Bureau, Michelle, Tassinari, Carlo Alberto

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A Novel Protein Tyrosine Phosphatase Gene Is Mutated in Progressive Myoclonus Epilepsy of the Lafora Type (EPM2) von Serratosa, José M., Gómez-Garre, Pilar, Gallardo, Ma Esther, Anta, Berta, de Bernabé, Daniel Beltrán-Valero, Lindhout, Dick, Augustijn, Paul B., Tassinari, Carlo A., Michelucci, Roberto, Malafosse, Alain, Topcu, Meral, Grid, Djamel, Dravet, Charlotte, Berkovic, Samuel F., de Córdoba, Santiago Rodríguez

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