Результати пошуку - Ozkara, Cigdem

Reflex epilepsy: triggers and management strategies за авторством Okudan, Zeynep Vildan, Özkara, Çiğdem

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Defining Clinico‐Neuropathological Subtypes of Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis за авторством Blümcke, Ingmar, Coras, Roland, Miyata, Hajime, Özkara, Cigdem

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Treatment of COVID‐19‐induced refractory status epilepticus by tocilizumab за авторством Kizilkilic, Esra Kochan, Unkun, Rumeysa, Uygunoglu, Ugur, Delil, Sakir, Ozkara, Cigdem

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Cytokine Polymorphism and HLA Genotyping in Patients with Temporal Lobe Epilepsy Related to Hippocampal Sclerosis за авторством ALTINTAŞ, Ayşe, ÖZKARA, Çiğdem, SOHTAOĞLU SEVİNDİK, Melis, UZAN, Mustafa, KEKİK ÇINAR, Çiğdem, UYSAL, Ömer, SAVRAN OĞUZ, Fatma

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Analysis of neurology consultations in hospitalized patients with COVID-19 за авторством Ser, Merve Hazal, Tanrıverdi, Uygur, Özkara, Çiğdem, Saip, Sabahattin, Aliş, Ceren, Güleç, Zeynep Ece Kaya, Nezir, Gözde, Kızılkılıç, Esra Koçhan, Süzgün, Merve Aktan, Abbaszade, Hikmet, Börekçi, Şermin, Karaali, Rıdvan, Kızılkılıç, Osman, Gündüz, Ayşegül, Savrun, Feray Karaali

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Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration за авторством Bilguvar, Kaya, Tyagi, Navneet K., Ozkara, Cigdem, Tuysuz, Beyhan, Bakircioglu, Mehmet, Choi, Murim, Delil, Sakir, Caglayan, Ahmet O., Baranoski, Jacob F., Erturk, Ozdem, Yalcinkaya, Cengiz, Karacorlu, Murat, Dincer, Alp, Johnson, Michele H., Mane, Shrikant, Chandra, Sreeganga S., Louvi, Angeliki, Boggon, Titus J., Lifton, Richard P., Horwich, Arthur L., Gunel, Murat

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The clinico-pathological spectrum of Focal Cortical Dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission за авторством Blümcke, Ingmar, Thom, Maria, Aronica, Eleonora, Armstrong, Dawna D., Vinters, Harry V., Palmini, Andre, Jacques, Thomas S, Avanzini, Giuliano, Barkovich, A. James, Battaglia, Giorgio, Becker, Albert, Cepeda, Carlos, Cendes, Fernando, Colombo, Nadia, Crino, Peter, Cross, J. Helen, Delalande, Olivier, Dubeau, François, Duncan, John, Guerrini, Renzo, Kahane, Philippe, Mathern, Gary, Najm, Imad, Özkara, Çiğdem, Raybaud, Charles, Represa, Alfonso, Roper, Steven N., Salamon, Noriko, Schulze-Bonhage, Andreas, Tassi, Laura, Vezzani, Annamaria, Spreafico, Roberto

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A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy за авторством 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

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