Immunotherapy In Autism Spectrum Disorder; A Case Series von Agdere, S. F., Topaloglu, P., Erata, M., Karacetin, G., Yapici, Z.

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Clinical characteristics of pediatric-onset neuro-Behçet disease von ULUDUZ, D, KÜRTÜNCÜ, M, YAPICI, Z, SEYAHI, E, KASAPCOPUR, Ö, ÖZDOGAN, H, SAIP, S, AKMAN-DEMIR, G, SIVA, A

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Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling von Toksoy, G, Durmus, H, Aghayev, A, Bagirova, G, Sevinc Rustemoglu, B, Basaran, S, Avci, S, Karaman, B, Parman, Y, Altunoglu, U, Yapici, Z, Tekturk, P, Deymeer, F, Topaloglu, H, Kayserili, H, Oflazer-Serdaroglu, P, Uyguner, ZO

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Fibromatous lesion of the scalp: is it an underestimated sign of tuberous sclerosis? von Baykal, C., Tekturk, P., Polat Ekinci, A., Buyukbabani, N., Baykan, B., Yapici, Z.

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Prevalence, phenotype and cardiometabolic risk of polycystic ovary syndrome under different diagnostic criteria von Yildiz, Bulent Okan, Bozdag, Gurkan, Yapici, Zuhal, Esinler, Ibrahim, Yarali, Hakan

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P103 – 2340: Atypical enterovirus encephalitis causing behavioral changes and autism-like clinical manifestations: Case report von Akcakaya, H, Tekturk, P, Tur, E.K, Eraksoy, M, Yapici, Z

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Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiency von Ortez, C., Duarte, S.T., Ormazábal, A., Serrano, M., Pérez, A., Pons, R., Pineda, M., Yapici, Z., Fernández-Álvarez, E., Domingo-Jiménez, R., De Castro, P., Artuch, R., García-Cazorla, A.

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Sustained reduction in seizure frequency with adjunctive everolimus for treatment-refractory seizures associated with tuberous sclerosis complex (TSC) in children under 6 years of... von Curatolo, P, Franz, D.N, Lawson, J.A, Yapici, Z, Ikeda, H, Polster, T, Nabbout, R, de Vries, P.J, Dlugos, D.J, Fan, J, Peyrard, S, Pelov, D, Voi, M, French, J.A

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High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease von Bilir, B, Yapici, Z, Yalcinkaya, C, Baris, I, Carvalho, CMB, Bartnik, M, Ozes, B, Eraksoy, M, Lupski, JR, Battaloglu, E

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PP12.5 – 2798: DBS-implanted PKAN cases: Two clinical observations von Yapici, Z, Tekturk, P, Ertan, S, Citak, A, Sik, G, Akcakaya, H, Eraksoy, M, Aydin, S

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Non-progressive congenital ataxia with cerebellar hypoplasia in three families von YAPICI, Z, ERAKSOY, M

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NEW GENES AND DISEASES: EP.302 Peptidylarginine deiminase 2 (PAD2) gene variant leading to abnormal myelination, and motor dysfunction von Eser, G., Celik, G., Ceylaner, S., Tuncali, T., Yapici, Z., Topaloglu, H.

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NEW GENES AND DISEASES von Eser, G., Celik, G., Ceylaner, S., Tuncali, T., Yapici, Z., Topaloglu, H.

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FP24-TU-03 Early IFNB-1b therapy in children with multiple sclerosis: a prospective study von Eraksoy, M, Ayta, S, Yapici, Z, Akman-Demır, G, Ozcan, H

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Panayiotopoulos syndrome and Gastaut syndrome are distinct entities in terms of neuropsychological findings von Akca Kalem, Sukriye, Elmali, Ayse Deniz, Demirbilek, Veysi, Oktem, Oget, Yapici, Zuhal, Saltik, Sema, Gokcay, Ahmet, Dervent, Aysin, Baykan, Betul

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Natural History of Vanishing White Matter von Hamilton, Eline M. C., van der Lei, Hannemieke D. W., Lourenço, Charles M., Naidu, Sakkubai, Mierzewska, Hanna, de Vet, Henrica C. W., Uitdehaag, Bernard M. J., Lissenberg‐Witte, Birgit I., Aldhalaan, H., Alves, D., Appleton, R., Arslan, E.A., Baethmann, M., Banwell, B., Barbot, C., Bertini, E., Bley, A., Bollen, L., Boltshauser, E., Bower, S., Bravo Oro, A., Campos, M.M., Carr, L., Chan, A.K.J., Clarke, A., Crow, Y., Csányi, B., Del Rossario Aldao, M., D'Hooghe, M., El Helou, J, Fallon, P., Ferlini, A., Ferro, J.M., Fluss, J., Fontenelle, L., Garone, C., Geldhoff, M., Glamuzina, E., Góes, F., Gonzalez, V., Guarda, C., Gulati, S., Güler, S., Horvath, R., Jagadeesh, S., Kaczorowska, M., Kankirawatana, P., Karall, D., King, M.D., Krägeloh‐Mann, I., Lehman, A., Liptai, Z., Livingston, J.H., Maes, M., Majumdar, A., Mandel, H., McEntagart, M., Morton, R., Moura de Souza, C.F., Mundy, H., Naess, K., Naismith, K., Newton, R.W., Noetzel, M.J., O'Brien, B, Okálová, K., Østergaard, J.R., Pato Pato, A., Pera, J., Perlman, S., Philippart, M., Régal, L., Rice, C.M., Rossignol, E., Rubin, J.P., Salvi, F., Sampaio, H., Sánchez Herrero, J., Santos, E., Sessa, M., Sharma, S., Shearn, J., Shoffner, J., Skranes, J.S., Sparagana, S.P., Storey, E., Sztriha, L., Tatli, B., Tekturk, P., Tennison, M., Tirupathi, S., Toledo Bravo de Laguna, L., Tuna, M.A., Valverde, A., van Coster, R., Vasconcelos, M., Vogt, H., von Kleist‐Retzow, J.C., Wong, S.S.N., Yavuz, H.

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Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy von VAN BERGE, Laura, HAMILTON, Eline M, DE JONG, Brigit A, MALAK AL GHAMDI, VAN WIERINGEN, Wessel N, TANNOUS, Bakhos A, HULLEMAN, Esther, WÜRDINGER, Thomas, VAN BERKEL, Carola G. M, POLDER, Emiel, ABBINK, Truus E. M, STRUYS, Eduard A, LINNANKIVI, Tarja, SCHEPER, Gert C, VAN DER KNAAP, Marjo S, UZIEL, Graziella, STEENWEG, Marjan E, ISOHANNI, Pirjo, WOLF, Nicole I, KRÄGELOH-MANN, Ingeborg, BRAUTASET, Nils J, ANDREWS, P. Ian

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance von Dibbens, Leanne M., Mullen, Saul, Helbig, Ingo, Mefford, Heather C., Bayly, Marta A., Bellows, Susannah, Leu, Costin, Trucks, Holger, Obermeier, Tanja, Wittig, Michael, Franke, Andre, Caglayan, Hande, Yapici, Zuhal, Sander, Thomas, Eichler, Evan E., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F.

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Two new cases with progressive cavitating leukoencephalopathy von Yapici, Z, Benbir, G, Saltik, S, Ertugrul, B, Naidu, S, Yalcinkaya, C

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HIGH INTERLEUKIN-10 PRODUCTION IS ASSOCIATED WITH ANTI-ACETYLCHOLINE RECEPTOR ANTIBODY PRODUCTION AND TREATMENT RESPONSE IN JUVENILE MYASTHENIA GRAVIS von YAPICI, Z., TÜZÜN, E., ALTUNAYO LU, V., ERDO AN, A., ERAKSOY, M.

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