A Widely Distributed Spectral Signature of Task-Negative Electrocorticography Responses Revealed during a Visuomotor Task in the Human Cortex

بواسطة Ramot, Michal, Fisch, Lior, Harel, Michal, Kipervasser, Svetlana, Andelman, Fani, Neufeld, Miri Y., Kramer, Uri, Fried, Itzhak, Malach, Rafael
الحاوية / القاعدة J Neurosci (2012)

Enhanced Category Tuning Revealed by Intracranial Electroencephalograms in High-Order Human Visual Areas

بواسطة Privman, Eran, Nir, Yuval, Kramer, Uri, Kipervasser, Svetlana, Andelman, Fani, Neufeld, Miri Y., Mukamel, Roy, Yeshurun, Yehezkel, Fried, Itzhak, Malach, Rafael
الحاوية / القاعدة J Neurosci (2007)

Spatial and Object-Based Attention Modulates Broadband High-Frequency Responses across the Human Visual Cortical Hierarchy

بواسطة Davidesco, Ido, Harel, Michal, Ramot, Michal, Kramer, Uri, Kipervasser, Svetlana, Andelman, Fani, Neufeld, Miri Y., Goelman, Gadi, Fried, Itzhak, Malach, Rafael
الحاوية / القاعدة J Neurosci (2013)

Emergence of Sensory Patterns during Sleep Highlights Differential Dynamics of REM and Non-REM Sleep Stages

بواسطة Ramot, Michal, Fisch, Lior, Davidesco, Ido, Harel, Michal, Kipervasser, Svetlana, Andelman, Fani, Neufeld, Miri Y., Kramer, Uri, Fried, Itzhak, Malach, Rafael
الحاوية / القاعدة J Neurosci (2013)

Neural “Ignition”: Enhanced Activation Linked to Perceptual Awareness in Human Ventral Stream Visual Cortex

بواسطة Fisch, Lior, Privman, Eran, Ramot, Michal, Harel, Michal, Nir, Yuval, Kipervasser, Svetlana, Andelman, Fani, Neufeld, Miri Y., Kramer, Uri, Fried, Itzhak, Malach, Rafael
منشور في 2009

Interhemispheric correlations of slow spontaneous neuronal fluctuations revealed in human sensory cortex

بواسطة Nir, Yuval, Mukamel, Roy, Dinstein, Ilan, Privman, Eran, Harel, Michal, Fisch, Lior, Gelbard-Sagiv, Hagar, Kipervasser, Svetlana, Andelman, Fani, Neufeld, Miri Y, Kramer, Uri, Arieli, Amos, Fried, Itzhak, Malach, Rafael
منشور في 2008

Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome

بواسطة Helbig, Ingo, Barcia, Giulia, Pendziwiat, Manuela, Ganesan, Shiva, Mueller, Stefanie H., Helbig, Katherine L., Vaidiswaran, Priya, Xian, Julie, Galer, Peter D., Afawi, Zaid, Specchio, Nicola, Kluger, Gerhard, Kuhlenbäumer, Gregor, Appenzeller, Silke, Wittig, Michael, Kramer, Uri, van Baalen, Andreas, Nabbout, Rima
الحاوية / القاعدة Ann Clin Transl Neurol (2020)

Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy

بواسطة Miyake, Noriko, Fukai, Ryoko, Ohba, Chihiro, Chihara, Takahiro, Miura, Masayuki, Shimizu, Hiroshi, Kakita, Akiyoshi, Imagawa, Eri, Shiina, Masaaki, Ogata, Kazuhiro, Okuno-Yuguchi, Jiu, Fueki, Noboru, Ogiso, Yoshifumi, Suzumura, Hiroshi, Watabe, Yoshiyuki, Imataka, George, Leong, Huey Yin, Fattal-Valevski, Aviva, Kramer, Uri, Miyatake, Satoko, Kato, Mitsuhiro, Okamoto, Nobuhiko, Sato, Yoshinori, Mitsuhashi, Satomi, Nishino, Ichizo, Kaneko, Naofumi, Nishiyama, Akira, Tamura, Tomohiko, Mizuguchi, Takeshi, Nakashima, Mitsuko, Tanaka, Fumiaki, Saitsu, Hirotomo, Matsumoto, Naomichi
الحاوية / القاعدة Am J Hum Genet (2016)

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization

بواسطة Afawi, Zaid, Oliver, Karen L., Kivity, Sara, Mazarib, Aziz, Blatt, Ilan, Neufeld, Miriam Y., Helbig, Katherine L., Goldberg-Stern, Hadassa, Misk, Adel J., Straussberg, Rachel, Walid, Simri, Mahajnah, Muhammad, Lerman-Sagie, Tally, Ben-Zeev, Bruria, Kahana, Esther, Masalha, Rafik, Kramer, Uri, Ekstein, Dana, Shorer, Zamir, Wallace, Robyn H., Mangelsdorf, Marie, MacPherson, James N., Carvill, Gemma L., Mefford, Heather C., Jackson, Graeme D., Scheffer, Ingrid E., Bahlo, Melanie, Gecz, Jozef, Heron, Sarah E., Corbett, Mark, Mulley, John C., Dibbens, Leanne M., Korczyn, Amos D., Berkovic, Samuel F.
الحاوية / القاعدة Neurology (2016)

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients

بواسطة de Kovel, Carolien G.F., Brilstra, Eva H., van Kempen, Marjan J.A., van‘t Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber
الحاوية / القاعدة Mol Genet Genomic Med (2016)