Women’s issues

由 Keni, Ravish, Mostacci, Barbara, Kiteva-Trenchevska, Gordana, Licchetta, Laura, Ignjatova, Liljana, Thomas, Sanjeev, Meador, Kimford J.
發表在 Epileptic Disord (2020)

Prevalence of Nocturnal Frontal Lobe Epilepsy in the Adult Population of Bologna and Modena, Emilia-Romagna Region, Italy

由 Vignatelli, Luca, Bisulli, Francesca, Giovannini, Giada, Licchetta, Laura, Naldi, Ilaria, Mostacci, Barbara, Rubboli, Guido, Provini, Federica, Tinuper, Paolo, Meletti, Stefano
發表在 Sleep (2015)

Clinical Features and Pathophysiology of Disorders of Arousal in Adults: A Window Into the Sleeping Brain

由 Baldini, Tommaso, Loddo, Giuseppe, Sessagesimi, Elisa, Mignani, Francesco, Cirignotta, Fabio, Mondini, Susanna, Licchetta, Laura, Bisulli, Francesca, Tinuper, Paolo, Provini, Federica
發表在 Front Neurol (2019)

Auditory aura in nocturnal frontal lobe epilepsy: a red flag to suspect an extra-frontal epileptogenic zone

由 Ferri, Lorenzo, Bisulli, Francesca, Nobili, Lino, Tassi, Laura, Licchetta, Laura, Mostacci, Barbara, Stipa, Carlotta, Mainieri, Greta, Bernabè, Giorgia, Provini, Federica, Tinuper, Paolo
發表在 Sleep Med (2014)

Incidence of sudden unexpected death in nocturnal frontal lobe epilepsy: a cohort study

由 Mostacci, Barbara, Bisulli, Francesca, Vignatelli, Luca, Licchetta, Laura, Di Vito, Lidia, Rinaldi, Claudia, Trippi, Irene, Ferri, Lorenzo, Plazzi, Giuseppe, Provini, Federica, Tinuper, Paolo
發表在 Sleep Med (2015)

Sleep-related hypermotor epilepsy: Long-term outcome in a large cohort

由 Licchetta, Laura, Bisulli, Francesca, Vignatelli, Luca, Zenesini, Corrado, Di Vito, Lidia, Mostacci, Barbara, Rinaldi, Claudia, Trippi, Irene, Naldi, Ilaria, Plazzi, Giuseppe, Provini, Federica, Tinuper, Paolo
發表在 Neurology (2017)

Treatment with metformin in twelve patients with Lafora disease

由 Bisulli, Francesca, Muccioli, Lorenzo, d’Orsi, Giuseppe, Canafoglia, Laura, Freri, Elena, Licchetta, Laura, Mostacci, Barbara, Riguzzi, Patrizia, Pondrelli, Federica, Avolio, Carlo, Martino, Tommaso, Michelucci, Roberto, Tinuper, Paolo
發表在 Orphanet J Rare Dis (2019)

The Impact of the COVID-19 Pandemic on People With Epilepsy. An Italian Survey and a Global Perspective

由 Mostacci, Barbara, Licchetta, Laura, Cacciavillani, Carlotta, Di Vito, Lidia, Ferri, Lorenzo, Menghi, Veronica, Stipa, Carlotta, Avoni, Patrizia, Provini, Federica, Muccioli, Lorenzo, Vignatelli, Luca, Mazzoni, Stefania, Tinuper, Paolo, Bisulli, Francesca
發表在 Front Neurol (2020)

Epilepsy with auditory features: A heterogeneous clinico-molecular disease

由 Pippucci, Tommaso, Licchetta, Laura, Baldassari, Sara, Palombo, Flavia, Menghi, Veronica, D'Aurizio, Romina, Leta, Chiara, Stipa, Carlotta, Boero, Giovanni, d'Orsi, Giuseppe, Magi, Alberto, Scheffer, Ingrid, Seri, Marco, Tinuper, Paolo, Bisulli, Francesca
發表在 Neurol Genet (2015)

Epilepsy in MT‐ATP6 ‐ related mils/NARP: correlation of elettroclinical features with heteroplasmy

由 Licchetta, Laura, Ferri, Lorenzo, La Morgia, Chiara, Zenesini, Corrado, Caporali, Leonardo, Lucia Valentino, Maria, Minardi, Raffaella, Fulitano, Daniela, Di Vito, Lidia, Mostacci, Barbara, Alvisi, Lara, Avoni, Patrizia, Liguori, Rocco, Tinuper, Paolo, Bisulli, Francesca, Carelli, Valerio
發表在 Ann Clin Transl Neurol (2021)

Encephalopathy in COVID-19 Presenting With Acute Aphasia Mimicking Stroke

由 Pensato, Umberto, Muccioli, Lorenzo, Pasini, Elena, Tappatà, Maria, Ferri, Lorenzo, Volpi, Lilia, Licchetta, Laura, Battaglia, Stella, Rossini, Giada, Bon, Isabella, Re, Maria Carla, Cirillo, Luigi, Simonetti, Luigi, Gramegna, Laura Ludovica, Michelucci, Roberto, Cortelli, Pietro, Zini, Andrea, Bisulli, Francesca
發表在 Front Neurol (2020)

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

由 Pippucci, Tommaso, Licchetta, Laura, Baldassari, Sara, Marconi, Caterina, De Luise, Monica, Myers, Candace, Nardi, Elena, Provini, Federica, Cameli, Cinzia, Minardi, Raffaella, Bacchelli, Elena, Giordano, Lucio, Crichiutti, Giovanni, d'Orsi, Giuseppe, Seri, Marco, Gasparre, Giuseppe, Mefford, Heather C., Tinuper, Paolo, Bisulli, Francesca
發表在 Ann Clin Transl Neurol (2019)

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

由 Tinuper, Paolo, Bisulli, Francesca, Cross, J.H., Hesdorffer, Dale, Kahane, Philippe, Nobili, Lino, Provini, Federica, Scheffer, Ingrid E., Tassi, Laura, Vignatelli, Luca, Bassetti, Claudio, Cirignotta, Fabio, Derry, Christopher, Gambardella, Antonio, Guerrini, Renzo, Halasz, Peter, Licchetta, Laura, Mahowald, Mark, Manni, Raffaele, Marini, Carla, Mostacci, Barbara, Naldi, Ilaria, Parrino, Liborio, Picard, Fabienne, Pugliatti, Maura, Ryvlin, Philippe, Vigevano, Federico, Zucconi, Marco, Berkovic, Samuel, Ottman, Ruth
發表在 Neurology (2016)

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

由 Muona, Mikko, Berkovic, Samuel F, Dibbens, Leanne M, Oliver, Karen L, Maljevic, Snezana, Bayly, Marta A, Joensuu, Tarja, Canafoglia, Laura, Franceschetti, Silvana, Michelucci, Roberto, Markkinen, Salla, Heron, Sarah E, Hildebrand, Michael S, Andermann, Eva, Andermann, Frederick, Gambardella, Antonio, Tinuper, Paolo, Licchetta, Laura, Scheffer, Ingrid E, Criscuolo, Chiara, Filla, Alessandro, Ferlazzo, Edoardo, Ahmad, Jamil, Ahmad, Adeel, Baykan, Betul, Said, Edith, Topcu, Meral, Riguzzi, Patrizia, King, Mary D, Ozkara, Cigdem, Andrade, Danielle M, Engelsen, Bernt A, Crespel, Arielle, Lindenau, Matthias, Lohmann, Ebba, Saletti, Veronica, Massano, João, Privitera, Michael, Espay, Alberto J, Kauffmann, Birgit, Duchowny, Michael, Møller, Rikke S, Straussberg, Rachel, Afawi, Zaid, Ben-Zeev, Bruria, Samocha, Kaitlin E, Daly, Mark J, Petrou, Steven, Lerche, Holger, Palotie, Aarno, Lehesjoki, Anna-Elina
發表在 Nat Genet (2014)

A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies

由 Baumgartner, Tobias, Carreño, Mar, Rocamora, Rodrigo, Bisulli, Francesca, Boni, Antonella, Brázdil, Milan, Horak, Ondrej, Craiu, Dana, Pereira, Cristina, Guerrini, Renzo, San Antonio‐Arce, Victoria, Schulze‐Bonhage, Andreas, Zuberi, Sameer M., Hallböök, Tove, Kalviainen, Reetta, Lagae, Lieven, Nguyen, Sylvie, Quintas, Sofia, Franco, Ana, Cross, J. Helen, Walker, Matthew, Arzimanoglou, Alexis, Rheims, Sylvain, Granata, Tiziana, Canafoglia, Laura, Johannessen Landmark, Cecilie, Sen, Arjune, Rattihalli, Rohini, Nabbout, Rima, Tartara, Elena, Santos, Manuela, Rangel, Rui, Krsek, Pavel, Marusic, Petr, Specchio, Nicola, Braun, Kees P. J., Smeyers, Patricia, Villanueva, Vicente, Kotulska, Katarzyna, Surges, Rainer, Tinuper, Paolo, Licchetta, Laura, Michelucci, Roberto, Toulouse, Joseph, Panagiotakaki, Eleni, Ostrowsky‐Coste, Karine, Lesca, Gaetan, de Curtis, Marco, Elisak, Martin, Domańska‐Pakiea, Dorota, Sadowski, Krzysztof
發表在 Epilepsia Open (2021)

Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

由 Corbett, Mark A., Kroes, Thessa, Veneziano, Liana, Bennett, Mark F., Florian, Rahel, Schneider, Amy L., Coppola, Antonietta, Licchetta, Laura, Franceschetti, Silvana, Suppa, Antonio, Wenger, Aaron, Mei, Davide, Pendziwiat, Manuela, Kaya, Sabine, Delledonne, Massimo, Straussberg, Rachel, Xumerle, Luciano, Regan, Brigid, Crompton, Douglas, van Rootselaar, Anne-Fleur, Correll, Anthony, Catford, Rachael, Bisulli, Francesca, Chakraborty, Shreyasee, Baldassari, Sara, Tinuper, Paolo, Barton, Kirston, Carswell, Shaun, Smith, Martin, Berardelli, Alfredo, Carroll, Renee, Gardner, Alison, Friend, Kathryn L., Blatt, Ilan, Iacomino, Michele, Di Bonaventura, Carlo, Striano, Salvatore, Buratti, Julien, Keren, Boris, Nava, Caroline, Forlani, Sylvie, Rudolf, Gabrielle, Hirsch, Edouard, Leguern, Eric, Labauge, Pierre, Balestrini, Simona, Sander, Josemir W., Afawi, Zaid, Helbig, Ingo, Ishiura, Hiroyuki, Tsuji, Shoji, Sisodiya, Sanjay M., Casari, Giorgio, Sadleir, Lynette G., van Coller, Riaan, Tijssen, Marina A. J., Klein, Karl Martin, van den Maagdenberg, Arn M. J. M., Zara, Federico, Guerrini, Renzo, Berkovic, Samuel F., Pippucci, Tommaso, Canafoglia, Laura, Bahlo, Melanie, Striano, Pasquale, Scheffer, Ingrid E., Brancati, Francesco, Depienne, Christel, Gecz, Jozef
發表在 Nat Commun (2019)

The landscape of epilepsy-related GATOR1 variants

由 Baldassari, Sara, Picard, Fabienne, Verbeek, Nienke E., van Kempen, Marjan, Brilstra, Eva H., Lesca, Gaetan, Conti, Valerio, Guerrini, Renzo, Bisulli, Francesca, Licchetta, Laura, Pippucci, Tommaso, Tinuper, Paolo, Hirsch, Edouard, de Saint Martin, Anne, Chelly, Jamel, Rudolf, Gabrielle, Chipaux, Mathilde, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Sisodiya, Sanjay, Balestrini, Simona, Schoeler, Natasha, Hernandez-Hernandez, Laura, Krithika, S., Oegema, Renske, Hagebeuk, Eveline, Gunning, Boudewijn, Deckers, Charles, Berghuis, Bianca, Wegner, Ilse, Niks, Erik, Jansen, Floor E., Braun, Kees, de Jong, Daniëlle, Rubboli, Guido, Talvik, Inga, Sander, Valentin, Uldall, Peter, Jacquemont, Marie-Line, Nava, Caroline, Leguern, Eric, Julia, Sophie, Gambardella, Antonio, d’Orsi, Giuseppe, Crichiutti, Giovanni, Faivre, Laurence, Darmency, Veronique, Benova, Barbora, Krsek, Pavel, Biraben, Arnaud, Lebre, Anne-Sophie, Jennesson, Mélanie, Sattar, Shifteh, Marchal, Cécile, Nordli, Douglas R, Lindstrom, Kristin, Striano, Pasquale, Lomax, Lysa Boissé, Kiss, Courtney, Bartolomei, Fabrice, Lepine, Anne Fabienne, Schoonjans, An-Sofie, Stouffs, Katrien, Jansen, Anna, Panagiotakaki, Eleni, Ricard-Mousnier, Brigitte, Thevenon, Julien, de Bellescize, Julitta, Catenoix, Hélène, Dorn, Thomas, Zenker, Martin, Müller-Schlüter, Karen, Brandt, Christian, Krey, Ilona, Polster, Tilman, Wolff, Markus, Balci, Meral, Rostasy, Kevin, Achaz, Guillaume, Zacher, Pia, Becher, Thomas, Cloppenborg, Thomas, Yuskaitis, Christopher J., Weckhuysen, Sarah, Poduri, Annapurna, Lemke, Johannes R., Møller, Rikke S., Baulac, Stéphanie
發表在 Genet Med (2018)

Correction: The landscape of epilepsy-related GATOR1 variants

由 Baldassari, Sara, Picard, Fabienne, Verbeek, Nienke E., van Kempen, Marjan, Brilstra, Eva H., Lesca, Gaetan, Conti, Valerio, Guerrini, Renzo, Bisulli, Francesca, Licchetta, Laura, Pippucci, Tommaso, Tinuper, Paolo, Hirsch, Edouard, de Saint Martin, Anne, Chelly, Jamel, Rudolf, Gabrielle, Chipaux, Mathilde, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Sisodiya, Sanjay, Balestrini, Simona, Schoeler, Natasha, Hernandez-Hernandez, Laura, Krithika, S., Oegema, Renske, Hagebeuk, Eveline, Gunning, Boudewijn, Deckers, Charles, Berghuis, Bianca, Wegner, Ilse, Niks, Erik H., Jansen, Floor E., Braun, Kees, de Jong, Daniëlle, Rubboli, Guido, Talvik, Inga, Sander, Valentin, Uldall, Peter, Jacquemont, Marie-Line, Nava, Caroline, Leguern, Eric, Julia, Sophie, Gambardella, Antonio, d’Orsi, Giuseppe, Crichiutti, Giovanni, Faivre, Laurence, Darmency, Veronique, Benova, Barbora, Krsek, Pavel, Biraben, Arnaud, Lebre, Anne-Sophie, Jennesson, Mélanie, Sattar, Shifteh, Marchal, Cécile, NordliJr, Douglas R, Lindstrom, Kristin, Striano, Pasquale, Lomax, Lysa Boissé, Kiss, Courtney, Bartolomei, Fabrice, Lepine, Anne Fabienne, Schoonjans, An-Sofie, Stouffs, Katrien, Jansen, Anna, Panagiotakaki, Eleni, Ricard-Mousnier, Brigitte, Thevenon, Julien, de Bellescize, Julitta, Catenoix, Hélène, Dorn, Thomas, Zenker, Martin, Müller-Schlüter, Karen, Brandt, Christian, Krey, Ilona, Polster, Tilman, Wolff, Markus, Balci, Meral, Rostasy, Kevin, Achaz, Guillaume, Zacher, Pia, Becher, Thomas, Cloppenborg, Thomas, Yuskaitis, Christopher J., Weckhuysen, Sarah, Poduri, Annapurna, Lemke, Johannes R., Møller, Rikke S., Baulac, Stéphanie
發表在 Genet Med (2018)

Correction to: The landscape of epilepsy-related GATOR1 variants

由 Baldassari, Sara, Picard, Fabienne, Verbeek, Nienke E., van Kempen, Marjan, Brilstra, Eva H., Lesca, Gaetan, Conti, Valerio, Guerrini, Renzo, Bisulli, Francesca, Licchetta, Laura, Pippucci, Tommaso, Tinuper, Paolo, Hirsch, Edouard, Martin, Anne de Saint, Chelly, Jamel, Rudolf, Gabrielle, Chipaux, Mathilde, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Sisodiya, Sanjay, Balestrini, Simona, Schoeler, Natasha, Hernandez-Hernandez, Laura, Krithika, S., Oegema, Renske, Hagebeuk, Eveline, Gunning, Boudewijn, Deckers, Charles, Berghuis, Bianca, Wegner, Ilse, Niks, Erik, Jansen, Floor, Braun, Kees, Jong, Daniëlle de, Rubboli, Guido, Talvik, Inga, Sander, Valentin, Uldall, Peter, Jacquemont, Marie-Line, Nava, Caroline, Leguern, Eric, Julia, Sophie, Gambardella, Antonio, d’Orsi, Giuseppe, Crichiutti, Giovanni, Faivre, Laurence, Darmency, Veronique, Benova, Barbora, Krsek, Pavel, Biraben, Arnaud, Lebre, Anne-Sophie, Jennesson, Mélanie, Sattar, Shifteh, Marchal, Cécile, NordliJr, Douglas R., Lindstrom, Kristin, Striano, Pasquale, Lomax, Lysa Boissé, Kiss, Courtney, Bartolomei, Fabrice, Lepine, Anne Fabienne, Schoonjans, An-Sofie, Stouffs, Katrien, Jansen, Anna, Panagiotakaki, Eleni, Ricard-Mousnier, Brigitte, Thevenon, Julien, Bellescize, Julitta de, Catenoix, Hélène, Dorn, Thomas, Zenker, Martin, Müller-Schlüter, Karen, Brandt, Christian, Krey, Ilona, Polster, Tilman, Wolff, Markus, Balci, Meral, Rostasy, Kevin, Achaz, Guillaume, Zacher, Pia, Becher, Thomas, Cloppenborg, Thomas, Yuskaitis, Christopher J., Weckhuysen, Sarah, Poduri, Annapurna, Lemke, Johannes R., Møller, Rikke S., Baulac, Stéphanie
發表在 Genet Med (2018)