The effectiveness and tolerability of clobazam in the pediatric population: Adjunctive therapy and monotherapy in a large-cohort multicenter study von Kamaşak, Tülay, Serdaroğlu, Esra, Yılmaz, Özlem, Kılıç, Betül Aydın, Polat, Burçin G., Erdoğan, Irmak, Yücel Şen, A.Derda, Özen, Nalan, Durgut, Betül Diler, Yıldız, Nihal, Özkan Kart, Pınar, Dilber, Beril, Arslan, Elif Acar, Şahin, Sevim, Topçu, Yasemin, Gencpinar, Pınar, Serin, H. Mine, Hız, Semra A., Çarman, Kürşat Bora, Dündar, Nihal Olgaç, Okuyaz, Çetin, Aydın, Kürşad, Serdaroğlu, Ayşe, Tekgül, Hasan, Cansu, Ali

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Neuromuscular disease genetics in under-represented populations: increasing data diversity von Wilson, Lindsay A, Macken, William L, Perry, Luke D, Record, Christopher J, Schon, Katherine R, Frezatti, Rodrigo S S, Raga, Sharika, Naidu, Kireshnee, Köken, Özlem Yayıcı, Polat, Ipek, Kapapa, Musambo M, Dominik, Natalia, Efthymiou, Stephanie, Morsy, Heba, Nel, Melissa, Fassad, Mahmoud R, Gao, Fei, Patel, Krutik, Schoonen, Maryke, Bisschoff, Michelle, Vorster, Armand, Jonvik, Hallgeir, Human, Ronel, Lubbe, Elsa, Nonyane, Malebo, Vengalil, Seena, Nashi, Saraswati, Srivastava, Kosha, Lemmers, Richard J L F, Reyaz, Alisha, Mishra, Rinkle, Töpf, Ana, Trainor, Christina I, Steyn, Elizabeth C, Mahungu, Amokelani C, van der Vliet, Patrick J, Ceylan, Ahmet Cevdet, Hiz, A Semra, Çavdarlı, Büşranur, Semerci Gündüz, C Nur, Ceylan, Gülay Güleç, Nagappa, Madhu, Tallapaka, Karthik B, Govindaraj, Periyasamy, van der Maarel, Silvère M, Narayanappa, Gayathri, Nandeesh, Bevinahalli N, Wa Somwe, Somwe, Bearden, David R, Kvalsund, Michelle P, Ramdharry, Gita M, Oktay, Yavuz, Yiş, Uluç, Topaloğlu, Haluk, Sarkozy, Anna, Bugiardini, Enrico, Henning, Franclo, Wilmshurst, Jo M, Heckmann, Jeannine M, McFarland, Robert, Taylor, Robert W, Smuts, Izelle, van der Westhuizen, Francois H, Sobreira, Claudia Ferreira da Rosa, Tomaselli, Pedro J, Marques, Jr, Wilson, Bhatia, Rohit, Dalal, Ashwin, Srivastava, M V Padma, Yareeda, Sireesha, Nalini, Atchayaram, Vishnu, Venugopalan Y, Thangaraj, Kumarasamy, Straub, Volker, Horvath, Rita, Chinnery, Patrick F, Pitceathly, Robert D S, Muntoni, Francesco, Houlden, Henry, Vandrovcova, Jana, Reilly, Mary M, Hanna, Michael G

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Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study von Kanmaz, Seda, Tekgul, Hasan, Kayilioglu, Hulya, Atas, Yavuz, Kart, Pinar Ozkan, Yildiz, Nihal, Gumus, Hakan, Aydin, Kursad, Kanmaz, Seda, Olculu, Cemile Busra, Dogan, Dilara Ece Toprak, Per, Huseyin, Canpolat, Mehmet, Gulec, Ayten, Yildirim, Nalan, Turk, Emre, Celik, Neslihan, Ozturk, Selcan, Kumandas, Sefer, Kilic, Betul, Topcu, Yasemin, Ozpinar, Esra, Coskun, Aysenur, Arslan, Mutluay, Akkoyunlu, Deniz Sunnetci, Cine, Naci, Uzan, Gamze Sarikaya, Gunay, Cagatay, Akyol, Duygu, Ersoy, Ozlem, Direk, Meltem Cobanogullari, Komur, Mustafa, Kirkgoz, Hilal, Karaoğlu, Pakize, Ibis, Ipek Burcu Parlak, Cerci, Cisil, Orak, Ali, Oktay, Secil, Ayanoglu, Muge, Yildirim, Mirac, Bektas, Omer, Serdaroglu, Esra, Yilmaz, Sema Bozkaya, Cankurt, Ilknur, Hirfanoglu, Tugba, Arhan, Ebru, Gencpinar, Pinar, Dundar, Nihal Olgac, Teber, Serap, Serin, Hepsen Mine, Yilmaz, Sanem, Tosun, Ayse, Polat, Muzaffer, Yilmaz, Unsal, Unalp, Aycan, Kara, Bulent, Okuyaz, Cetin, Yis, Uluc, Hiz, Semra, Aktan, Gul, Gokben, Sarenur, Unay, Bulent, Serdaroglu, Ayse, Cansu, Ali

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Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes von Yılmaz, Ünsal, Gücüyener, Kıvılcım, Yavuz, Merve, Öncel, İbrahim, Saltık, Sema, Ünver, Olcay, Yılmaz, Sanem, Erol, İlknur, Öztoprak, Ülkühan, Elitez, Duygu Aykol, Direk, Meltem Çobanoğulları, Bodur, Muhittin, Teber, Serap, Yılmaz, Ünsal, Anlar, Banu, Gücüyener, Kıvılcım, Ünver, Olcay, Çıtak Kurt, Ayşegül Neşe, Tosun, Ayşe, Yılmaz, Sanem, Özgör, Bilge, Öztoprak, Ülkühan, Aykol, Duygu, Yıldız, Edibe Pembegül, Yarar, Coşkun, Haspolat, Şenay, İncecik, Faruk, Kutluk, Gültekin, Dundar, Nihal Olgac, Öncel, İbrahim, Demir, Ercan, Türkdoğan, Dilşad, Yalnızoğlu, Dilek, Akbaş, Salih, Güleç, Ayten, Yılmaz, Deniz, Ayanoğlu, Müge, Kanmaz, Seda, Beşen, Şeyda, Öztürk, Selcan, Yüksel, Deniz, Gürkaş, Esra, Oktay, Seçil, Serin, Hepsen Mine, Karadağ, Meral, Hakkı Akbeyaz, İsmail, Yiş, Uluç, Polat, Burçin Gönüllü, Okan, Mehmet Sait, Bektaş, Ömer, Orgun, Leman Tekin, Günbey, Ceren, Gültutan, Pembe, Aksoy, Erhan, Akyüz, Gülcan, Tekgül, Hasan, Kürekçi, Fulya, Kurul, A. Semra Hız, Çarman, Kürşat Bora, Duman, Özgür, Kömür, Mustafa, Yıldırım, Miraç, Alıcı, Nurettin, Gümüş, Hakan, Polat, Muzaffer, Konuşkan, Bahadır, Güngör, Olcay, Mert, Gülen Gül, Edizer, Selvinaz, Mıhçı, Filiz, Yavuz, Merve, Toker, Rabia Tütüncü, Şahin, Sevim, Gencpinar, Pinar, Yıldırım, Elif, Yüksel, Ersin, Ekici, Arzu, Deniz, Adnan, Yayici Köken, Özlem, Okuyaz, Çetin, Süt, Nurşah Yeniay, Atasoy, Ergin, Yetkin, Mehmet Fatih, Bilgin, Neslihan, Tekin, Hande Gazeteci, Özçelik, Aysima, Türköz, Ayşe Nur, Cavusoglu, Dilek, Özkan, Mehbare, Tekin, Emine, Koç, Habibe, Sarıgeçili, Esra, Sarıtaş, Serdar, Ayça, Senem, Şenoğlu, Mine Çiğdem, Kamaşak, Tülay, Keskin, Filiz, Karaoğlu, Pakize, İpek, Rojan, Acer, Hamit

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Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity von Matalonga, Leslie, Laurie, Steven, Papakonstantinou, Anastasios, Piscia, Davide, Mereu, Elisabetta, Bullich, Gemma, Thompson, Rachel, Horvath, Rita, Pérez-Jurado, Luis, Riess, Olaf, Gut, Ivo, van Ommen, Gert-Jan, Lochmüller, Hanns, Beltran, Sergi, Renieri, Alessandra, Dursun, Ali, Matilla-Duenas, Antoni, Cormand, Bru, Rivolta, Carlo, Ayuso, Carmen, Espinós, Carmen, Scerri, Christian, Yalnizoglu, Dilek, Soler, Doriette, Morava, Eva, Barbetti, Fabrizio, Forzano, Francesca, Mari, Francesca, Muntoni, Francesco, Tort, Frederic, Houlden, Henry James, Tejada, Maria-Isabel, Senderek, Jan, Benitez, Javier, De La Calle, Javier Corral, Serra, Jordi, Millán, José Ma, Segovia, Jose, Gimeno Blanes, Juan Ramon, Armstrong, Judith, Ozgul, Koksal, Vilarinho, Laura, Montoliu, Lluis, Posada, Manuel, Mencarelli, Maria Antonietta, Mora, Marina, Bianchi, Paola, Seeman, Pavel, Elliott, Perry M., Ferlini, Alessandra, Brice, Alexis, Wirth, Brunhilde, Hanna, Mike, Tabrizi, Sarah, Klockgether, Thomas, Timmerman, Vincent, Straub, Volker, Kurul, Semra Hiz, Oktay, Yavuz, Gungor, Serdal, Yaramis, Ahmet, Yis, Uluc, Macaya, Alfons, Ribes, Antonia, Pujol, Aurora, Lázaro, Conxi, Grinberg, Daniel, Tizzano, Eduardo, Cardellach, Francesc, Palau, Francesc, Milà, Montse, Gallano, Pia, Artuch, Rafael, MartiSeves, Ramon, Villanueva, Gonzalo, Vidal, Silvia, Garrabou, Gloria, Balcells, Susanna, Urreizti, Roser, López, Estrella, Cuscó, Ivon, Valenzuela, Irene, Sabater, Maria

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Neuromuscular disease genetics in under-represented populations: increasing data diversity von Wilson, Lindsay A, Macken, William L, Perry, Luke D, Record, Christopher J, Schon, Katherine R, Frezatti, Rodrigo SS, Raga, Sharika, Naidu, Kireshnee, Köken, Özlem Yayıcı, Polat, Ipek, Kapapa, Musambo M, Dominik, Natalia, Efthymiou, Stephanie, Morsy, Heba, Nel, Melissa, Fassad, Mahmoud R, Gao, Fei, Patel, Krutik, Schoonen, Maryke, Bisschoff, Michelle, Vorster, Armand, Jonvik, Hallgeir, Human, Ronel, Lubbe, Elsa, Nonyane, Malebo, Vengalil, Seena, Nashi, Saraswati, Srivastava, Kosha, Lemmers, Richard JLF, Reyaz, Alisha, Mishra, Rinkle, Töpf, Ana, Trainor, Christina I, Steyn, Elizabeth C, Mahungu, Amokelani C, van der Vliet, Patrick J, Ceylan, Ahmet Cevdet, Hiz, A Semra, Çavdarlı, Büşranur, Semerci Gündüz, C Nur, Ceylan, Gülay Güleç, Nagappa, Madhu, Tallapaka, Karthik B, Govindaraj, Periyasamy, van der Maarel, Silvère M, Narayanappa, Gayathri, Nandeesh, Bevinahalli N, Wa Somwe, Somwe, Bearden, David R, Kvalsund, Michelle P, Ramdharry, Gita M, Oktay, Yavuz, Yiş, Uluç, Topaloğlu, Haluk, Sarkozy, Anna, Bugiardini, Enrico, Henning, Franclo, Wilmshurst, Jo M, Heckmann, Jeannine M, McFarland, Robert, Taylor, Robert W, Smuts, Izelle, van der Westhuizen, Francois H, Sobreira, Claudia Ferreira da Rosa, Tomaselli, Pedro J, Marques, Wilson, Bhatia, Rohit, Dalal, Ashwin, Srivastava, MV Padma, Yareeda, Sireesha, Nalini, Atchayaram, Vishnu, Venugopalan Y, Thangaraj, Kumarasamy, Straub, Volker, Horvath, Rita, Chinnery, Patrick F, Pitceathly, Robert DS, Muntoni, Francesco, Houlden, Henry, Vandrovcova, Jana, Reilly, Mary M, Hanna, Michael G

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Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial von Chitnis, Tanuja, Banwell, Brenda, Kappos, Ludwig, Arnold, Douglas L, Gücüyener, Kivilcim, Deiva, Kumaran, Skripchenko, Natalia, Cui, Li-Ying, Saubadu, Stephane, Hu, Wenruo, Benamor, Myriam, Le-Halpere, Annaig, Truffinet, Philippe, Tardieu, Marc, Dubois, Benedicte, Verhelst, Helene, Bojinova-Tchamova, Veneta, Mah, Jean, Cui, Li-Ying, Fang, Fang, Hao, Yunpeng, Jiang, Li, Li, Ling, Mao, Ding'An, Qiu, Wei, Tan, Guojun, Wu, Ye, Zhang, Meini, Zhou, Hongyu, Zhou, Shuizhen, Gross-Paju, Katrin, Cheuret, Emmanuel, Deiva, Kumaran, Edan, Giles, Vukusic, Sandra, Chrousos, George, Zafeiriou, Dimitrios, Achiron, Anat, Vaknin-Dembinsky, Adi, Yamout, Bassem, Laurynaitiene, Jurate, Vaiciene-Magistris, Nerija, Bojkovski, Vladimir, Trajkova, Vesna, Chaouki, Sana, Kissani, Najib, Neuteboom, Rinze, Palavra, Filipe, Belova, Anna, Boyko, Alexey, Evdoshenko, Evgeny, Kairbekova, Ekaterina, Malkova, Nadezhda, Shumilina, Maria, Skripchenko, Natalya, Nikolic, Dimitrije, Meca-Lallana, Jose, Triki, Chahnez Charfi, Chokri, Mhiri, Gouider, Riadh, Anlar, Banu, Gücüyener, Kivilcim, Hiz, Ayse Semra, Idiman, Egemen, Turkoglu, Recai, Yapici, Zuhal, Yilmaz, Unsal, Tantsura, Lyudmyla, Voloshyna, Nataliia, Lim, Ming, Wassmer, Evangeline, Cascione, Mark, Chitnis, Tanuja, LaGanke, Christopher, Rathke, Kevin, Scagnelli, John

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Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database von Yılmaz, Ünsal, Anlar, Banu, Gücüyener, Kıvılcım, Yaramış, Ahmet, Cansu, Ali, Ünalp, Aycan, Aksoy, Ayşe, Bayram, Ayşe Kaçar, Kartal, Ayşe, Tosun, Ayşe, Serdaroğlu, Ayşe, Konuşkan, Bahadır, Sarıoğlu, Berrak, Yüzbaşı, Beste Kıpçak, Kılıç, Betül, Taşkın, Birce Dilge, Bulut, Cahide, Yılmaz, Cahide, Yarar, Coşkun, Okuyaz, Çetin, Gençsel, Çigdem, Yüksel, Deniz, Arslan, Elif Acar, Gürkaş, Esra, Faruk incecik, Serdaroğlu, Gül, Deda, Gülhis, Gürbüz, Gürkan, Gümüş, Hakan, Acer, Hamit, Tekgül, Hasan, Çaksen, Hüseyin, Per, Hüseyin, Erol, İlknur, Çarman, Kürşat Bora, Canpolat, Mehmet, Özkan, Mehpare, Direk, Meltem Çobanoğulları, Kutluk, Muhammet Gültekin, Arslan, Mutluay, Sönmez, F. Müjgan, Dündar, Nihal Olgaç, Koçak, Ozan, Aydın, Ömer Faruk, Toptaş, Özge, Duman, Özgür, Hergüner, Özlem, Bozkurt, Öznur, Arıcan, Pınar, Yılmaz, Sanem, Gökben, Sarenur, Işıkay, Sedat, Kumandaş, Sefer, Edizer, Selvinaz, Kurul, Semra Hız, Saygı, Semra, Teber, Serap, Güngör, Serdal, Altunbaşak, Şakir, Haspolat, Şenay, Sezer, Taner, Yılmaz, Tuba Sevim, Yiş, Uluç, Öztoprak, Ülkühan, Aydoğmuş, Ümmü, Topçu, Yasemin, Öztürk, Zeynep, Karalök, Zeynep Selen

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The fate of spikes in self-limited epilepsy with centrotemporal spikes: Are clinical and baseline EEG features effective? von Günay, Çağatay, Sarikaya Uzan, Gamze, Özsoy, Özlem, Hiz Kurul, Semra, Yiş, Uluç

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High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases von Hiz Kurul, Semra, Oktay, Yavuz, Töpf, Ana, Szabó, Nóra Zs, Güngör, Serdal, Yaramis, Ahmet, Sonmezler, Ece, Matalonga, Leslie, Yis, Uluc, Schon, Katherine, Paramonov, Ida, Kalafatcilar, İpek Polat, Gao, Fei, Rieger, Aliz, Arslan, Nur, Yilmaz, Elmasnur, Ekinci, Burcu, Edem, Pinar Pulat, Aslan, Mahmut, Özgör, Bilge, Lochmüller, Angela, Nair, Ashwati, O'Heir, Emily, Lovgren, Alysia K, Maroofian, Reza, Houlden, Henry, Polavarapu, Kiran, Roos, Andreas, Müller, Juliane S, Hathazi, Denisa, Chinnery, Patrick F, Laurie, Steven, Beltran, Sergi, Lochmüller, Hanns, Horvath, Rita

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An Unusual Presentation of Leber Hereditary Optic Neuropathy-Plus Case Caused by a Novel DNAJC30 Variant von Şenol, Hüseyin Bahadır, Soydemir, Didem, Polat, Ayşe İpek, Aydın, Adem, Hız, Ayşe Semra, Yiş, Uluç

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Electroclinical and Demographic Evaluation of Cases with Selflimited Epilepsy with Centrotemporal Spikes von Meryem BADEM, Gamze SARIKAYA UZAN, Semra HIZ KURUL

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Expanding the genotypic and phenotypic spectrum of the SPTBN4 gene mutation: A new variant and dysmorphology von Günay, Çağatay, Onay, Hüseyin, Bademkıran, Fikret, Hız Kurul, Semra, Yiş, Uluç

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Inflammation and endothelial dysfunction in pediatric migraine patients von Polat, İpek, Karaoğlu, Pakize, Şişman, Ali Rıza, Yiş, Uluç, Hız Kurul, Semra

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Clinical predictors of drug-resistant epilepsy in children von Karaoglu, Pakize, Yis, Uluc, Polat, Ayse Ipek, Ayanoglu, Muge, Hiz, Semra

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High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases von Kurul, Semra Hiz, Matalonga, Leslie, Paramonov, Ida, Laurie, Steven, 1973, Beltran, Sergi, Lochmüller, Hanns, Horvath, Rita

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Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA von Karaoglu, Pakize, Quizon, Nicolas, Pergande, Matthias, Wang, Haicui, Polat, Ayşe Ipek, Ersen, Ayca, Özer, Erdener, Willkomm, Lena, Hiz Kurul, Semra, Heredia, Raúl, Yis, Uluç, Selcen, Duygu, Çirak, Sebahattin

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Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy von Gursoy, Semra, Ataman, Esra, Baysal, Bahar, Özyılmaz, Berk, Gençpınar, Pınar, Hız, Ayşe, Yiş, Uluç, Ünalp, Aycan, Dündar, Nihal, Ülgenalp, Ayfer, Erçal, Derya

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Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects von Arlt, Annabelle, Kohlschmidt, Nicolai, Hentschel, Andreas, Bartels, Enrika, Groß, Claudia, Töpf, Ana, Edem, Pınar, Szabo, Nora, Sickmann, Albert, Meyer, Nancy, Schara-Schmidt, Ulrike, Lau, Jarred, Lochmüller, Hanns, Horvath, Rita, Oktay, Yavuz, Roos, Andreas, Hiz, Semra

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Severe neurodevelopmental disease caused by a homozygous TLK2 variant von Topf, Ana, Oktay, Yavuz, Balaraju, Sunitha, Yilmaz, Elmasnur, Sonmezler, Ece, Yis, Uluc, Laurie, Steven, Thompson, Rachel, Roos, Andreas, MacArthur, Daniel G., Yaramis, Ahmet, Gungor, Serdal, Lochmueller, Hanns, Hiz, Semra, Horvath, Rita

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