Subacute Sclerosing Panencephalitis Mimicking Posterior Circulation Ischemic Stroke von Gor, Zeynep, Uzunhan, Tuğçe A, Yapici, Ozge, Ozek, Sibel U, Hamilcikan, Berna

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Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings von Aksu Uzunhan, Tuğçe, Ayaz, Akif

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Disrupted oxidative stress resistance: A homozygous mutation in the catalytic (TLDc) domain of TBC1D24 gene associated with epileptic encephalopathy von Uzunhan, Tuğçe Aksu, Uyanik, Bülent

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Generalized Peripheric Nerve Hyperexcitability with Neuropathy: Case Series with Long-Term Outcome von Akan, Onur, Baysal, Leyla, Uzunhan, Tuğçe Aksu, Tüzün, Erdem

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First afebrile seizures: Clinical and radiological view with emergent testing von Aksu Uzunhan, Tuğçe, Kaçar, Alper, Mısırlı Özdemir, Ebru, Yapıcı, Özge

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Cytotoxic lesions of the corpus callosum in children: Etiology, clinical and radiological features, and prognosis von Aksu Uzunhan, Tuğçe, Maraş Genç, Hülya, Kutlubay, Büşra, Kalın, Sevinç, Bektaş, Gonca, Yapıcı, Özge, Çıracı, Saliha, Sözen, Hatice Gülhan, Şevketoğlu, Esra, Palabıyık, Figen, Gör, Zeynep, Çakar, Nafiye Emel, Kara, Bülent

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A genetic mimic of cerebral palsy: Homozygous NFU1 mutation with marked intrafamilial phenotypic variation von Uzunhan, Tuğçe Aksu, Çakar, Nafiye Emel, Seyhan, Serhat, Aydin, Kürşad

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A case of juvenile Canavan disease with distinct pons involvement von Çakar, Nafiye Emel, Aksu Uzunhan, Tuğçe

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Short‐term neurological outcomes in ischemic and hemorrhagic pediatric stroke von Uzunhan, Tuğçe Aksu, Aydinli, Nur, Çalişkan, Mine, Tatli, Burak, Özmen, Meral

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Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome von Aksu Uzunhan, Tuğçe, Ertürk, Biray, Aydın, Kürşad, Ayaz, Akif, Altunoğlu, Umut, Yarar, Murat Hakkı, Gezdirici, Alper, İçağasıoğlu, Dilara Füsun, Gökpınar İli, Ezgi, Uyanık, Bülent, Eser, Metin, Kutbay, Yaşar Bekir, Topçu, Yasemin, Kılıç, Betül, Bektaş, Gonca, Arduç Akçay, Ayfer, Ekici, Barış, Chousein, Amet, Avcı, Şahin, Yüksel, Atıl, Kayserili, Hülya

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Pediatric Guillain-Barré syndrome: Indicators for a severe course von Varkal, Muhammet Ali, Uzunhan, Tuğçe Aksu, Aydınlı, Nur, Ekici, Barış, Çalışkan, Mine, Özmen, Meral

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The role of cranial magnetic resonance imaging findings in pediatric epilepsy: A single-center experience von Yapici, Ozge, Uzunhan, Tugce Aksu

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Cobalamin E disease with a novel homozygous MTRR mutation as a cobalamin-related remethylation disorder: a treatable etiology in West syndrome von Aksu Uzunhan, Tuğçe, Uyanık, Bülent, Ersoy, Melike, Türkmenoğlu, Yelda

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A Rare Cause of Acute Cerebellar Ataxia: Familial Hemophagocytic Lymphohistiocytosis von Aksu Uzunhan, Tuğçe, MD, Çalışkan, Mine, MD, Karaman, Serap, MD, Aydın, Kubilay, MD, Devecioğlu, Ömer, MD

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Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up von Bektaş, Gonca, Yeşil, Gözde, Özkan, Melis Ulak, Yıldız, Edibe Pembegül, Uzunhan, Tuğçe Aksu, Çalışkan, Mine

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The relationship between epileptic seizure and melatonin in children von Tarcin, Gurkan, Aksu Uzunhan, Tugce, Kacar, Alper, Kucur, Mine, Saltik, Sema

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Efficacy and Side Effect Profile of Clobazam in Children with Different Etiologies of Epilepsy from a Single Center von Uzunhan, Tugce Aksu, Gor, Zeynep

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Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia von Ayaz, Akif, Uzunhan, Tugce Aksu, Aydin, Kursad

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Lacosamide treatment of childhood refractory focal epilepsy: the first reported side effect in paediatric patients von Yildiz, Edibe Pembegul, Ozkan, Melis Ulak, Bektas, Gonca, Uzunhan, Tuğçe Aksu, Aydinli, Nur, Caliskan, Mine, Ozmen, Meral

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A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy von Altuntaş, Cansu, Uzunhan, Tugce Aksu, Ertürk, Biray, Petmezci, Mey Talip, Çakar, Nafiye Emel, Noyan, Bilge, Dokucu, Ali İhsan, Önal, Hasan

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