Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A von Kara, Bülent, Köroğlu, Çiğdem, Peltonen, Karita, Steinberg, Ruchama C, Maraş Genç, Hülya, Hölttä-Vuori, Maarit, Güven, Ayşe, Kanerva, Kristiina, Kotil, Tuğba, Solakoğlu, Seyhun, Zhou, You, Olkkonen, Vesa M, Ikonen, Elina, Laiho, Marikki, Tolun, Aslıhan

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Clinical and neuroradiologic variability of Aicardi-Goutiéres syndrome: Two siblings with RNASEH2C mutation and a boy with TREX1 mutation von Uyur Yalçın, Emek, Maraş Genç, Hülya, Kara, Bülent

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TSEN54 gene-related pontocerebellar hypoplasia type 2 presenting with exaggerated startle response: report of two cases in a family von Maraş-Genç, Hülya, Uyur-Yalçın, Emek, Rosti, Rasim Özgür, Gleeson, Joseph G, Kara, Bülent

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Mild encephalitis/encephalopathy with a reversible splenial lesion in children von Yildiz, Adalet Elcin, Genc, Hulya Maras, Gurkas, Esra, Unlu, Havva Akmaz, Oncel, Ibrahim Halil, Guven, Alev

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Clinical Outcomes in Children with Herpes Simplex Encephalitis Receiving Steroid Therapy von Genç, Hülya Maraş, Yalçın, Emek Uyur, Sayan, Murat, Bayhan, Asuman, Öncel, Selim, Arısoy, Emin Sami, Kara, Bülent

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BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy von Kara, Bülent, Uyguner, Oya, Maraş Genç, Hülya, İşlek, Eylül Ece, Kasap, Murat, Toksoy, Güven, Akpınar, Gürler, Uyur Yalçın, Emek, Anık, Yonca, Üstek, Duran

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Triple X Syndrome with a Rare Finding: Cleft Palate von Gurkas, Esra, Genc, Hulya Maras, Kilic, Esra

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Atropa Belladonna Poisoning in a Child with Acute Psychiatric Findings von Cebeci, Dilek, Gürkaş, Esra, Maraş Genç, Hülya, Ceylan, Nesrin

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Long-term Clinical and Radiologic Follow-Up of Schilder's Disease von Genç, Hülya Maraş, Kara, Bülent, Yalçın, Emek Uyur, Güneş, Ayfer Sakarya, Deniz, Adnan, Anık, Yonca

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Diagnostic yield of muscle biopsy in infants: Retrospective analysis of clinical and histopathologic findings von Genc, Hulya Maras, Guven, Alev, Talim, Beril

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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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Neurodevelopmental Outcome in Patients with Typical Imaging Features of Injury as a Result of Neonatal Hypoglycemia von Yalçın, Emek Uyur, Genç, Hülya Maraş, Bayhan, Asuman, Anık, Yonca, Kara, Bülent

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Evaluation of the short-term effects on bone mineral metabolism and the adrenal pathway of adrenocorticotropic hormone therapy used in epileptic encephalopathy von GÜNGÖR, Mesut, ALTINORDU, Bengü, MARAŞ GENÇ, Hülya, UYUR YALÇIN, Emek, ÇİZMECİOĞLU JONES, Filiz Mine, KARA, Bülent

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Pyruvate dehydrogenase-E1α deficiency presenting as recurrent acute proximal muscle weakness of upper and lower extremities in an 8-year-old boy von Kara, Bülent, Genç, Hülya Maraş, Uyur-Yalçın, Emek, Sakarya-Güneş, Ayfer, Topçu, Uğur, Mülayim, Serap, Ceylaner, Serdar

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Machine learning models for predicting treatment response in infantile epilepsies von Pembegul Yildiz, Edibe, Coskun, Orhan, Kurekci, Fulya, Maras Genc, Hulya, Ozaltin, Oznur

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A rare cause of arterial hypertension in a child with developmental delay: Questions von Pehlivanoglu, Cemile, Maras Genc, Hulya, Kalın, Sevinc

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A rare cause of arterial hypertension in a child with developmental delay: Answers von Pehlivanoglu, Cemile, Maras Genc, Hulya, Kalın, Sevinc

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Chronic inflammatory demyelinating neuropathy after etanercept therapy in the course of juvenile idiopathic arthritis von Genç, Hülya Maraş, Kutlubay, Büşra, Sürmeli, Reyhan, Sözen, Hatice Gülhan, Sözeri, Betül

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Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects von Kurekci, Fulya, Akif Kilic, Mehmet, Akbas, Sinan, Avci, Rıdvan, Oney, Ceyda, Dilruba Aslanger, Ayca, Maras Genc, Hulya, Aydinli, Nur, Pembegul Yildiz, Edibe

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Vanishing white matter disease with different faces von Güngör, Gülay, Güngör, Olcay, Çakmaklı, Seda, Maraş Genç, Hülya, İnce, Hülya, Yeşil, Gözde, Dilber, Cengiz, Aydın, Kürşad

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