Αποτελέσματα αναζήτησης - Rubboli, Guido
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Is autopsy tissue a valid control for epilepsy surgery tissue in microRNA studies? από Roncon, Paolo, Zucchini, Silvia, Ferracin, Manuela, Marucci, Gianluca, Giulioni, Marco, Michelucci, Roberto, Rubboli, Guido, Simonato, Michele
Έκδοση 2016Κείμενο -
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Prevalence of Nocturnal Frontal Lobe Epilepsy in the Adult Population of Bologna and Modena, Emilia-Romagna Region, Italy από Vignatelli, Luca, Bisulli, Francesca, Giovannini, Giada, Licchetta, Laura, Naldi, Ilaria, Mostacci, Barbara, Rubboli, Guido, Provini, Federica, Tinuper, Paolo, Meletti, Stefano
Έκδοση 2015Κείμενο -
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Mutant BRAF in low-grade epilepsy-associated tumors and focal cortical dysplasia από Marucci, Gianluca, de Biase, Dario, Visani, Michela, Giulioni, Marco, Martinoni, Matteo, Volpi, Llilia, Riguzzi, Patrizia, Rubboli, Guido, Michelucci, Roberto, Tallini, Giovanni
Έκδοση 2014Κείμενο -
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Recovery from Emotion Recognition Impairment after Temporal Lobectomy από Benuzzi, Francesca, Zamboni, Giovanna, Meletti, Stefano, Serafini, Marco, Lui, Fausta, Baraldi, Patrizia, Duzzi, Davide, Rubboli, Guido, Tassinari, Carlo Alberto, Nichelli, Paolo Frigio
Έκδοση 2014Κείμενο -
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Identification of miRNAs Differentially Expressed in Human Epilepsy with or without Granule Cell Pathology από Zucchini, Silvia, Marucci, Gianluca, Paradiso, Beatrice, Lanza, Giovanni, Roncon, Paolo, Cifelli, Pierangelo, Ferracin, Manuela, Giulioni, Marco, Michelucci, Roberto, Rubboli, Guido, Simonato, Michele
Έκδοση 2014Κείμενο -
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PRICKLE2 revisited—further evidence implicating PRICKLE2 in neurodevelopmental disorders από Bayat, Allan, Iqbal, Sumaiya, Borredy, Kim, Amiel, Jeanne, Zweier, Christiane, Barcia, Guilia, Kraus, Cornelia, Weyhreter, Heike, Bassuk, Alexander G., Chopra, Maya, Rubboli, Guido, Møller, Rikke S.
Έκδοση 2021Κείμενο -
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MicroRNA profiles in hippocampal granule cells and plasma of rats with pilocarpine-induced epilepsy – comparison with human epileptic samples από Roncon, Paolo, Soukupovà, Marie, Binaschi, Anna, Falcicchia, Chiara, Zucchini, Silvia, Ferracin, Manuela, Langley, Sarah R., Petretto, Enrico, Johnson, Michael R., Marucci, Gianluca, Michelucci, Roberto, Rubboli, Guido, Simonato, Michele
Έκδοση 2015Κείμενο -
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Epilepsy associated tumors: Review article από Giulioni, Marco, Marucci, Gianluca, Martinoni, Matteo, Marliani, Anna Federica, Toni, Francesco, Bartiromo, Fiorina, Volpi, Lilia, Riguzzi, Patrizia, Bisulli, Francesca, Naldi, Ilaria, Michelucci, Roberto, Baruzzi, Agostino, Tinuper, Paolo, Rubboli, Guido
Έκδοση 2014Κείμενο -
13
Mild malformations of cortical development in sleep‐related hypermotor epilepsy due to KCNT1 mutations από Rubboli, Guido, Plazzi, Giuseppe, Picard, Fabienne, Nobili, Lino, Hirsch, Edouard, Chelly, Jamel, Prayson, Richard A., Boutonnat, Jean, Bramerio, Manuela, Kahane, Philippe, Dibbens, Leanne M., Gardella, Elena, Baulac, Stéphanie, Møller, Rikke S.
Έκδοση 2018Κείμενο -
14
Deep-Phenotyping the Less Severe Spectrum of PIGT Deficiency and Linking the Gene to Myoclonic Atonic Seizures από Bayat, Allan, Pendziwiat, Manuela, Obersztyn, Ewa, Goldenberg, Paula, Zacher, Pia, Döring, Jan Henje, Syrbe, Steffen, Begtrup, Amber, Borovikov, Artem, Sharkov, Artem, Karasińska, Aneta, Giżewska, Maria, Mitchell, Wendy, Morava, Eva, Møller, Rikke S., Rubboli, Guido
Έκδοση 2021Κείμενο -
15
Electromagnetic source imaging in presurgical workup of patients with epilepsy: A prospective study από Duez, Lene, Tankisi, Hatice, Hansen, Peter Orm, Sidenius, Per, Sabers, Anne, Pinborg, Lars H., Fabricius, Martin, Rásonyi, György, Rubboli, Guido, Pedersen, Birthe, Leffers, Anne-Mette, Uldall, Peter, Jespersen, Bo, Brennum, Jannick, Henriksen, Otto Mølby, Fuglsang-Frederiksen, Anders, Beniczky, Sándor
Έκδοση 2019Κείμενο -
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Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders από Döring, Jan H., Schröter, Julian, Jüngling, Jerome, Biskup, Saskia, Klotz, Kerstin A., Bast, Thomas, Dietel, Tobias, Korenke, G. Christoph, Christoph, Sophie, Brennenstuhl, Heiko, Rubboli, Guido, Møller, Rikke S., Lesca, Gaetan, Chaix, Yves, Kölker, Stefan, Hoffmann, Georg F., Lemke, Johannes R., Syrbe, Steffen
Έκδοση 2021Κείμενο -
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Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy από Wengert, Eric R., Tronhjem, Cathrine E., Wagnon, Jacy L., Johannesen, Katrine M, Petit, Hayley, Krey, Ilona, Saga, Anusha U., Panchal, Payal S., Strohm, Samantha M., Lange, Jörn, Kamphausen, Susanne B, Rubboli, Guido, Lemke, Johannes R., Gardella, Elena, Patel, Manoj K., Meisler, Miriam H., Møller, Rikke S.
Έκδοση 2019Κείμενο -
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Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy από Møller, Rikke S., Weckhuysen, Sarah, Chipaux, Mathilde, Marsan, Elise, Taly, Valerie, Bebin, E. Martina, Hiatt, Susan M., Prokop, Jeremy W., Bowling, Kevin M., Mei, Davide, Conti, Valerio, de la Grange, Pierre, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Lambrecq, Virginie, Larsen, Line H.G., Leguern, Eric, Guerrini, Renzo, Rubboli, Guido, Cooper, Gregory M., Baulac, Stéphanie
Έκδοση 2016Κείμενο -
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Treatment Responsiveness in KCNT1-Related Epilepsy από Fitzgerald, Mark P., Fiannacca, Martina, Smith, Douglas M., Gertler, Tracy S., Gunning, Boudewijn, Syrbe, Steffen, Verbeek, Nienke, Stamberger, Hannah, Weckhuysen, Sarah, Ceulemans, Berten, Schoonjans, An-Sofie, Rossi, Massimiliano, Demarquay, Geneviève, Lesca, Gaetan, Olofsson, Kern, Koolen, D. A., Hornemann, Frauke, Baulac, Stephanie, Rubboli, Guido, Minks, Kelly Q., Lee, Bohoon, Helbig, Ingo, Dlugos, Dennis, Møller, Rikke S., Bearden, David
Έκδοση 2019Κείμενο -
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Standardized Computer-based Organized Reporting of EEG: SCORE από Beniczky, Sándor, Aurlien, Harald, Brøgger, Jan C, Fuglsang-Frederiksen, Anders, Martins-da-Silva, António, Trinka, Eugen, Visser, Gerhard, Rubboli, Guido, Hjalgrim, Helle, Stefan, Hermann, Rosén, Ingmar, Zarubova, Jana, Dobesberger, Judith, Alving, Jørgen, Andersen, Kjeld V, Fabricius, Martin, Atkins, Mary D, Neufeld, Miri, Plouin, Perrine, Marusic, Petr, Pressler, Ronit, Mameniskiene, Ruta, Hopfengärtner, Rüdiger, Emde Boas, Walter, Wolf, Peter
Έκδοση 2013Κείμενο