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Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay.
Kim M, Sandford E, Gatica D, Qiu Y, Liu X, Zheng Y, Schulman BA, Xu J, Semple I, Ro SH, Kim B, Mavioglu RN, Tolun A, Jipa A, Takats S, Karpati M, Li JZ, Yapici Z, Juhasz G, Lee JH, Klionsky DJ, Burmeister M. Kim M, et al. Among authors: yapici z. Elife. 2016 Jan 26;5:e12245. doi: 10.7554/eLife.12245. Elife. 2016. PMID: 26812546 Free PMC article.
Diagnosis of comorbid migraine without aura in patients with idiopathic/genetic epilepsy based on the gray zone approach to the International Classification of Headache Disorders 3 criteria.
Atalar AÇ, Özge A, Türk BG, Ekizoğlu E, Kurt Gök D, Baykan B, Ayta S, Erdoğan FF, Yeni SN, Taşdelen B; IDEM Study Group; Velioğlu SK. Atalar AÇ, et al. Front Neurol. 2023 Jan 10;13:1103541. doi: 10.3389/fneur.2022.1103541. eCollection 2022. Front Neurol. 2023. PMID: 36703639 Free PMC article.
De novo 8p23.1 deletion in a patient with absence epilepsy.
Akcakaya NH, Capan ÖY, Schulz H, Sander T, Caglayan SH, Yapıcı Z. Akcakaya NH, et al. Among authors: yapici z. Epileptic Disord. 2017 Jun 1;19(2):217-221. doi: 10.1684/epd.2017.0906. Epileptic Disord. 2017. PMID: 28533195
Clinical characteristics of pediatric-onset neuro-Behçet disease.
Uluduz D, Kürtüncü M, Yapıcı Z, Seyahi E, Kasapçopur Ö, Özdoğan H, Saip S, Akman-Demir G, Siva A. Uluduz D, et al. Among authors: yapici z. Neurology. 2011 Nov 22;77(21):1900-5. doi: 10.1212/WNL.0b013e318238edeb. Epub 2011 Nov 9. Neurology. 2011. PMID: 22076549
122 results