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

Volltext

Application of foliar urea to grapevines: productivity and flavour components of grapes von Gutiérrez‐Gamboa, G., Diez‐Zamudio, F., Stefanello, L. Oliveira, Tassinari, A., Brunetto, G.

Volltext

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

Volltext

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.

Volltext

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

Volltext

Cross-sectional DXA and MR measures of tibial periarticular bone associate with radiographic knee osteoarthritis severity von Lo, G.H, Tassinari, A.M, Driban, J.B, Price, L.L, Schneider, E, Majumdar, S, McAlindon, T.E

Volltext

Neuroethological approach to frontolimbic epileptic seizures and parasomnias: The same central pattern generators for the same behaviours von Tassinari, C.A., Cantalupo, G., Högl, B., Cortelli, P., Tassi, L., Francione, S., Nobili, L., Meletti, S., Rubboli, G., Gardella, E.

Volltext

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

Volltext

Sudden unexpected death in epilepsy (SUDEP) and sleep von Nobili, Lino, Proserpio, Paola, Rubboli, Guido, Montano, Nicola, Didato, Giuseppe, Tassinari, Carlo A

Volltext

Bone marrow lesions are associated with altered trabecular morphometry von Driban, J.B, Tassinari, A, Lo, G.H, Price, L.L, Schneider, E, Lynch, J.A, Eaton, C.B, McAlindon, T.E

Volltext

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

Volltext

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.

Volltext

Remission of encephalopathy with status epilepticus (ESES) during sleep renormalizes regulation of slow wave sleep von Bölsterli, Bigna K., Gardella, Elena, Pavlidis, Elena, Wehrle, Flavia M., Tassinari, Carlo A., Huber, Reto, Rubboli, Guido

Volltext

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.

Volltext

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

Volltext

Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1 von TESSA, C, MICHELUCCI, R, DE FEO, M. R, GIALLONARDO, A. T, TASSINARI, C. A, MASCALCHI, M, NOBILE, C, GIANNELLI, M, NAVE, R. Della, TESTONI, S, BIANUCCI, D, TINUPER, P, BISULLI, F, SOFIA, V

Volltext

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

Volltext

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 von Chapelle, Albert de la, Dieguez-Lucena, José L, Myers, Richard M, Pennacchio, Len A, Koskiniemi, Marjaleena, Tassinari, Carlo A, D'Amato, Elena, Michelucci, Roberto, Omer, Salah, Avanzini, Giuliano, Franceschetti, Silvana, Krahe, Ralf, Lehesjoki, Anna-Elina, Norio, Reijo, Miao, Jinmin, Virtaneva, Kimmo

Volltext

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.

Volltext

Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES) von Bonardi, Claudia M., Mignot, Cyril, Serratosa, Jose M., Giraldez, Beatriz G., Moretti, Raffaella, Rudolf, Gabrielle, Reale, Chiara, Gellert, Pia M., Johannesen, Katrine M., Lesca, Gaetan, Tassinari, Carlo A., Gardella, Elena, Møller, Rikke S., Rubboli, Guido

Volltext