Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia von Ghosh, Shereen G., Breuss, Martin W., Schlachetzki, Zinayida, Chai, Guoliang, Ross, Danica, Stanley, Valentina, Sonmez, F. Mujgan, Topaloglu, Haluk, Zaki, Maha S., Hosny, Heba, Gad, Shaimaa, Gleeson, Joseph G.

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Insomnia, parasomnia, and predisposing factors in Turkish school children von Ozgun, Nezir, Sonmez, F Mujgan, Topbas, Murat, Can, Gamze, Goker, Zeynep

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Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly von Uctepe, Eyyup, Vona, Barbara, Esen, Fatma Nisa, Sonmez, F Mujgan, Smol, Thomas, Tümer, Sait, Mancılar, Hanifenur, Geylan Durgun, Dilan Ece, Boute, Odile, Moghbeli, Meysam, Ghayoor Karimiani, Ehsan, Hashemi, Narges, Bakhshoodeh, Behnoosh, Kim, Hyung Goo, Maroofian, Reza, Yesilyurt, Ahmet

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Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study von Cavusoglu, Dilek, Ozturk, Gulten, Turkdogan, Dilsad, Kurul, Semra Hiz, Yis, Uluc, Komur, Mustafa, Incecik, Faruk, Kara, Bulent, Sahin, Turkan, Unver, Olcay, Dilber, Cengiz, Mert, Gulen Gul, Gunay, Cagatay, Uzan, Gamze Sarikaya, Ersoy, Ozlem, Oktay, Yavuz, Mermer, Serdar, Tuncer, Gokcen Oz, Gungor, Olcay, Ozcora, Gul Demet Kaya, Gumus, Ugur, Sezer, Ozlem, Cetin, Gokhan Ozan, Demir, Fatma, Yilmaz, Arzu, Gurbuz, Gurkan, Topcu, Meral, Topaloglu, Haluk, Ceylan, Ahmet Cevdet, Ceylaner, Serdar, Gleeson, Joseph G., Icagasioglu, Dilara Fusun, Sonmez, F. Mujgan

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Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene von Turan, Betül, Göktaş, Emine, Sönmez, F. Mujgan, Aydin, Halil Ibrahim, Aydogdu, Demet, Zamani, Ayse Gul, Yildirim, Mahmut Selman

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Epilepsy prevalence in the 0-17 age group in trabzon, Turkey von Topbaş, Murat, Ozgün, Sükrü, Sönmez, Müjgan F, Aksoy, Ayşe, Can, Gamze, Yavuzyilmaz, Asuman, Can, Emine

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Vitamin D deficiency in healthy children and adolescents von Orun, Emel, Sezer, Seyma, Kanburoglu, M Kenan, Namuslu, Mehmet, Sonmez, F Mujgan

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A novel mutation in guanidinoacetate methyltransferase (GAMT) deficiency in two patients associated with epilepsy, developmental delay, hyperactivity, autistic behavior von Aydin, Halil Ibrahim, Sonmez, F. Mujgan

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The Role of the Vitamin D in Neurology: Interrelationships Between Headache, Epilepsy and Vitamin D Deficiency von Sonmez, F. Mujgan

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The effects of antiepileptic drugs on the relationships between leptin levels and bone turnover in prepubertal children with epilepsy von Aksoy, Ayse, Sönmez, F. Müjgan, Deger, Orhan, Hosver, Ilgın, Karagüzel, Gülay

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A CASE OF CHICKENPOX ASSOCIATED WITH ACUTE PERIPHERAL FACIAL NERVE PALSY von Mujgan Sonmez, F, Aksoy, A

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Impact of Childhood Epilepsy on the Family von Kerim Fazlıoglu, Cicek Hocaoglu, F. Mujgan Sonmez

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P149 The effects of antiepileptic drugs on the relationships between leptin levels and bone markers in children with epilepsy von Aksoy, A, Sonmez, F. Mujgan, Hosver, I, Deger, O, Karaguzel, G

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Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly von Uctepe, Eyyup, Vona, Barbara, Esen, Fatma Nisa, Sonmez, F Mujgan, Smol, Thomas, Tümer, Sait, Mancılar, Hanifenur, Geylan Durgun, Dilan Ece, Boute, Odile, Moghbeli, Meysam, Ghayoor Karimiani, Ehsan, Hashemi, Narges, Bakhshoodeh, Behnoosh, Kim, Hyung Goo, Maroofian, Reza, Yesilyurt, Ahmet

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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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Tracing immature myelin in acute disseminated encephalomyelitis von Anlar, Banu, Karli-Oğuz, Kader, Yurtyapan, Osman Yücel, Senbil, Nesrin, Hergüner, Ozlem, Altunbaşak, Sakir, Sönmez, F Müjgan, Ozdemir-Geyik, Pinar

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Çocukluk Çagi Epilepsisinin Aileye Etkisi/Impact of Childhood Epilepsy on the Family von Fazlioglu, Kerim, Hocaoglu, Çiçek, Sönmez, F Müjgan

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Impact of Childhood Epilepsy on the Family von Fazlıoğlu, Kerim, Hocaoğlu, Çiçek, Sönmez, F. Müjgan

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Çocukluk Çağı Epilepsisinin Aileye Etkisi von Hocaoğlu,Çiçek, Fazlıoğlu,Kerim, Sönmez,F. Müjgan

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The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome von van der Sluijs, Pleuntje J., Jansen, Sandra, Vergano, Samantha A., Adachi-Fukuda, Miho, Alanay, Yasemin, AlKindy, Adila, Baban, Anwar, Bayat, Allan, Beck-Wödl, Stefanie, Berry, Katherine, Bijlsma, Emilia K., Bok, Levinus A., Brouwer, Alwin F. J., van der Burgt, Ineke, Campeau, Philippe M., Canham, Natalie, Chrzanowska, Krystyna, Dahan, Karin, De Rademaeker, Marjan, Destree, Anne, Dudding-Byth, Tracy, Earl, Rachel, Elcioglu, Nursel, Elias, Ellen R., Fagerberg, Christina, Gardham, Alice, Gener, Blanca, Gerkes, Erica H., Grasshoff, Ute, van Haeringen, Arie, Heitink, Karin R., Herkert, Johanna C., den Hollander, Nicolette S., Horn, Denise, Hunt, David, Kant, Sarina G., Kato, Mitsuhiro, Kayserili, Hülya, Kersseboom, Rogier, Kilic, Esra, Krajewska-Walasek, Malgorzata, Lammers, Kylin, Laulund, Lone W., Lederer, Damien, Lees, Melissa, López-González, Vanesa, Maas, Saskia, Mancini, Grazia M. S., Marcelis, Carlo, Martinez, Francisco, Maystadt, Isabelle, McGuire, Marianne, McKee, Shane, Mehta, Sarju, Metcalfe, Kay, Mizuno, Seiji, Moeschler, John B., Netzer, Christian, Ockeloen, Charlotte W., Oehl-Jaschkowitz, Barbara, Okamoto, Nobuhiko, Olminkhof, Sharon N. M., Orellana, Carmen, Pasquier, Laurent, Pottinger, Caroline, Riehmer, Vera, Robertson, Stephen P., Roifman, Maian, Rooryck, Caroline, Ropers, Fabienne G., Rosello, Monica, Ruivenkamp, Claudia A. L., Sagiroglu, Mahmut S., Sallevelt, Suzanne C. E. H., Sanchis Calvo, Amparo, Simsek-Kiper, Pelin O., Soares, Gabriela, Solaeche, Lucia, Sonmez, Fatma Mujgan, Splitt, Miranda, Steenbeek, Duco, Stegmann, Alexander P. A., Stumpel, Constance T. R. M., Tanabe, Saori, Uctepe, Eyyup, Utine, G. Eda, Veenstra-Knol, Hermine E., Venkateswaran, Sunita, Vincent-Delorme, Catherine, Vulto-van Silfhout, Anneke T., Wheeler, Patricia, Wilson, Golder N., Wilson, Louise C., Wollnik, Bernd, Kosho, Tomoki, Wieczorek, Dagmar, Eichler, Evan, Pfundt, Rolph, de Vries, Bert B. A., Santen, Gijs W. E.

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