Intravenous levetiracetam for treatment of seizures in term and preterm neonates von Karaoglu, Pakize, Hız, Semra, İşcan, Burçin, Polat, Ayşe, Ayanoğlu, Müge, Duman, Nuray, Yiş', Uluç

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Lissencephaly With Brainstem and Cerebellar Hypoplasia and Congenital Cataracts von Yis, Uluc

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Double trouble: A case of DYT-TOR1A diagnosed in the postoperative period von Uzan, Gamze, Günay, Çağatay, Kurul, Semra, Yiş, Uluç

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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Anaemia‐based screening for resistance to thyroid hormone alpha in children von Kağızmanlı, Gözde Akın, Kırbıyık, Özgür, Abacı, Ayhan, Böber, Ece, Yiş, Uluç, Demir, Korcan

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Biallelic variant in AGTPBP1 causes infantile lower motor neuron degeneration and cerebellar atrophy von Karakaya, Mert, Paketci, Cem, Altmueller, Janine, Thiele, Holger, Hoelker, Irmgard, Yis, Uluc, Wirth, Brunhilde

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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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Neuroprotective Effects of Lacosamide and Memantine on Hyperoxic Brain Injury in Rats von Polat, İpek, Cilaker Mıcılı, Serap, Çalışır, Meryem, Bayram, Erhan, Yiş, Uluç, Ayanoğlu, Müge, Okur, Derya, Edem, Pınar, Paketçi, Cem, Tuğyan, Kazım, Yılmaz, Osman, Hız Kurul, Semra

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Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation von Rohrbach, Marianne, Vandersteen, Anthony, Yiş, Uluç, Serdaroglu, Gul, Ataman, Esra, Chopra, Maya, Garcia, Sixto, Jones, Kristi, Kariminejad, Ariana, Kraenzlin, Marius, Marcelis, Carlo, Baumgartner, Matthias, Giunta, Cecilia

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Utility of Optical Genome Mapping in Repeat Disorders von Mutlu, Mehmet Burak, Karakaya, Taner, Çelebi, Hamide Betül Gerik, Duymuş, Fahrettin, Seyhan, Serhat, Yılmaz, Sanem, Yiş, Uluç, Atik, Tahir, Yetkin, Mehmet Fatih, Gümüş, Hakan

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Hypertrophic neuropathy of Sciatic nerve von Yiş, Uluç, Arslan, Mutluay, Güleryüz, Handan

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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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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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A boy with neck weakness von Yiş, Uluç, Becker, Kerstin, Çırak, Sebahattin

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COL12A1 Gene Variant and a Review of the Literature: A Case Report of Ullrich Congenital Muscular Dystrophy von İpek, Rojan, Çavdartepe, Büşra Eser, Bozdoğan, Sevcan Tuğ, Yiş, Uluç

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Safety and Efficacy of Nusinersen Focusing on Renal and Hematological Parameters in Spinal Muscular Atrophy von Bahadır Şenol, Hüseyin, Yıldız, Gizem, Polat, Ayşe İpek, Aydın, Adem, Hız, Ayşe Semra, Soylu, Alper, Yiş, Uluç

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A Novel HERC2 Variant in Two Siblings with Autosomal Recessive Intellectual Developmental Disorder-38 and Cardiomyopathy von Şenol, Hüseyin Bahadır, Günay, Çağatay, Polat, Ayşe İpek, Aydın, Adem, Hiz, Ayşe Semra, Yiş, Uluç

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What is the safe observation period for seizure recurrence in pediatric emergency departments? von Ulusoy, Emel, Uysal Ateş, Şebnem, Çitlenbik, Hale, Öztürk, Ali, Şık, Nihan, Arslan, Gazi, Yılmaz, Durgül, Yiş, Uluç, Hız, Semra, Duman, Murat

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Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders von Armirola-Ricaurte, Camila, Zonnekein, Noortje, Koutsis, Georgios, Amor-Barris, Silvia, Pelayo-Negro, Ana Lara, Atkinson, Derek, Efthymiou, Stephanie, Turchetti, Valentina, Dinopoulos, Argyris, Garcia, Antonio, Karakaya, Mert, Moris, German, Polat, Ayşe Ipek, Yiş, Uluç, Espinos, Carmen, Van de Vondel, Liedewei, De Vriendt, Els, Karadima, Georgia, Wirth, Brunhilde, Hanna, Michael, Houlden, Henry, Berciano, Jose, Jordanova, Albena

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A Novel PNPLA2 Variant in a Female Patient with Neutral Lipid Storage Disease with Myopathy and Hypogonadotropic Hypogonadism von Şenol, Hüseyin Bahadır, Kısa, Pelin Teke, Kulu, Bahar, Ören, Hale, Arslan, Nur, Yiş, Uluç

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