Comparison of physical fitness, activity, and quality of life of the children with epilepsy and their healthy peers von Sırtbaş, Gülsen, Yalnızoğlu, Dilek, Livanelioğlu, Ayşe

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations von Lifton, Richard P, State, Matthew W, Günel, Murat, Bilgüvar, Kaya, Öztürk, Ali Kemal, Louvi, Angeliki, Kwan, Kenneth Y, Choi, Murim, Tatl, Burak, Yaln zo lu, Dilek, Tüysüz, Beyhan, Ça layan, Ahmet Okay, Gökben, Sarenur, Kaymakçalan, Hande, Barak, Tanyeri, Bak rc o lu, Mehmet, Yasuno, Katsuhito, Ho, Winson, Sanders, Stephan, Zhu, Ying, Y lmaz, Sanem, Dinçer, Alp, Johnson, Michele H, Bronen, Richard A, Koçer, Naci, Per, Hüseyin, Mane, Shrikant, Pamir, Mehmet Necmettin, Yalç nkaya, Cengiz, Kumanda, Sefer, Topçu, Meral, Özmen, Meral, Šestan, Nenad

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Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span von Yücel-Yılmaz, Didem, Yücesan, Emrah, Yalnızoğlu, Dilek, Oğuz, Kader Karlı, Sağıroğlu, Mahmut Şamil, Özbek, Uğur, Serdaroğlu, Esra, Bilgiç, Başar, Erdem, Sevim, İşeri, Sibel Aylin Uğur, Hanağası, Haşmet, Gürvit, Hakan, Özgül, Rıza Köksal, Dursun, Ali

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Lesional resective epilepsy surgery in childhood: Comparison of two decades and long-term seizure outcome from a single center von Günbey, Ceren, Bilginer, Burçak, Oğuz, Kader Karlı, Söylemezoğlu, Figen, Ergün, Eser Lay, Akalan, Nejat, Topçu, Meral, Turanlı, Güzide, Yalnızoğlu, Dilek

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Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency von Yıldız, Yılmaz, Ardıçlı, Didem, Göçmen, Rahşan, Yalnızoğlu, Dilek, Topçu, Meral, Coşkun, Turgay, Tokatlı, Ayşegül, Haliloğlu, Göknur

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Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10 von Gürbüz, Berrak Bilginer, Gülbakan, Basri, Özgül, Rıza Köksal, Yalnızoğlu, Dilek, Yılmaz, Didem Yücel, Göçmen, Rahşan, Koşukcu, Can, Kandemir, Nurgün, Acar, Neşe Vardar, Salih, Bekir, Dursun, Ali

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Glucose Transporter Type 1 Deficiency Syndrome: A Single-Center Case Series von Yıldırım, Miraç, Babayiğit, Ömür, Ilgaz, Fatma, Yalnızoğlu, Dilek, Topçu, Meral

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International consensus classification of hippocampal sclerosis and etiologic diversity in children with temporal lobectomy von Günbey, Ceren, Söylemezoğlu, Figen, Bilginer, Burçak, Karlı Oğuz, Kader, Akalan, Nejat, Topçu, Meral, Turanlı, Güzide, Yalnızoğlu, Dilek

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Clinically important intracranial abnormalities in children presenting with first focal seizure von Kasap, Tuba, Tekşam, Özlem, Turanlı, Güzide, Konuşkan, Bahadır, Oğuz, Kader Karlı, Haliloğlu, Göknur, Yalnızoğlu, Dilek

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Behavioral problems of preschool children with new-onset epilepsy and one-year follow-up — A prospective study von Çelen Yoldaş, Tuba, Günbey, Ceren, Değerliyurt, Aydan, Erol, Neşe, Özmert, Elif, Yalnızoğlu, Dilek

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Clinical highlights of a very rare phospolipid remodeling disease due to MBOAT7 gene defect von Dursun, Ali, Yalnızoğlu, Dilek, Özgül, Rıza K., Karlı Oğuz, Kader, Yücel‐Yılmaz, Didem

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ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia von Deveci, Kübra, Yalnızoğlu, Dilek, Çağdaş, Deniz, Oğuz, Kader Karlı, Ertuğrul, İlker, Gülşen, Hayriye Hızarcıoğlu, Ocak, Melike, Bildik, Hacer Neslihan, Esenboğa, Saliha, Tezcan, İlhan

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Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defect von Yalnızoǧlu, Dilek, Özgül, R. Köksal, Oǧuz, Kader K., Özer, Buǧra, Yücel‐Yılmaz, Didem, Gürbüz, Berrak, Serdaroǧlu, Esra, Erol, İlknur, Topçu, Meral, Dursun, Ali

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Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation von Eroglu, Fehime K., Ozaltin, Fatih, Gönç, Nazlı, Nalçacıoğlu, Hülya, Özçakar, Z. Birsin, Yalnızoğlu, Dilek, Güçer, Şafak, Orhan, Diclehan, Eminoğlu, Fatma Tuba, Göçmen, Rahşan, Alikaşifoğlu, Ayfer, Topaloğlu, Rezan, Düzova, Ali

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Synthetic MRI in children with tuberous sclerosis complex von Coban, Gokcen, Gumeler, Ekim, Parlak, Safak, Konuskan, Bahadir, Karakaya, Jale, Yalnizoglu, Dilek, Anlar, Banu, Oguz, Kader K.

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Electrical status epilepticus during sleep: A study of 22 patients von Değerliyurt, Aydan, Yalnizoğlu, Dilek, Bakar, Emel Erdoğan, Topçu, Meral, Turanli, Güzide

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Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review von Laçinel Gürlevik, Sibel, Günbey, Ceren, Ozsurekci, Yasemin, Oygar, Pembe Derin, Kesici, Selman, Gocmen, Rahsan, Aydin, Orkun, Temucin, Çağrı, Tufan, Erennur, Terzi, Kıvanc, Baltu, Demet, Ozturk, Tugba Tastemel, Teksam, Ozlem, Ozen, Seza, Oguz, Kader Karlı, Cengiz, Ali Bulent, Yalnızoglu, Dilek

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Mesenchymal stem cell application in children with subacute sclerosing panencephalitis von Kuşkonmaz, Bariş, Uçkan, Duygu, Yalnizoğlu, Dilek, Günel, Mintaze, Karli Oğuz, Kader, Konuşkan, Bahadir, Anlar, Banu

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Neurologic outcome in patients with MRI pattern of damage typical for neonatal hypoglycemia von Yalnizoglu, Dilek, Haliloglu, Goknur, Turanli, Guzide, Cila, Ayşenur, Topcu, Meral

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Neurologic manifestations in children with COVID-19 von Gürlevik, Sibel Laçinel, Günbey, Ceren, Ozsurekci, Yasemin, Kesici, Selman, Gocmen, Rahsan, Temucin, Çağrı, Özen, Seza, Cengiz, Ali Bulent, Yalnızoglu, Dilek

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