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Treatment of Chorea in Childhood.
Yilmaz S, Mink JW. Yilmaz S, et al. Pediatr Neurol. 2020 Jan;102:10-19. doi: 10.1016/j.pediatrneurol.2019.08.013. Epub 2019 Sep 7. Pediatr Neurol. 2020. PMID: 31604647 Review.
Mitochondrial Membrane Protein-Associated Neurodegeneration.
Yilmaz S, Gokben S, Ceylaner S. Yilmaz S, et al. Pediatr Neurol. 2015 Oct;53(4):373-4. doi: 10.1016/j.pediatrneurol.2015.06.012. Epub 2015 Jun 21. Pediatr Neurol. 2015. PMID: 26231266 No abstract available.
The Utility of Genetic Testing in Infantile Epileptic Spasms Syndrome: A Step-Based Approach in the Next-Generation Sequencing Era.
Kanmaz S, Yılmaz S, Olculu CB, Toprak DE, Ince T, Yılmaz Ö, Atas Y, Sen G, Şimşek E, Serin HM, Durmuşalioğlu EA, Işık E, Atik T, Aktan G, Cogulu O, Gokben S, Ozkınay F, Tekgul H. Kanmaz S, et al. Among authors: yilmaz s, yilmaz o. Pediatr Neurol. 2024 Aug;157:100-107. doi: 10.1016/j.pediatrneurol.2024.05.018. Epub 2024 May 31. Pediatr Neurol. 2024. PMID: 38905742
Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights.
Yiş U, Becker K, Kurul SH, Uyanik G, Bayram E, Haliloğlu G, Polat Aİ, Ayanoğlu M, Okur D, Tosun AF, Serdaroğlu G, Yilmaz S, Topaloğlu H, Anlar B, Cirak S, Engel AG. Yiş U, et al. Among authors: yilmaz s. J Child Neurol. 2017 Jul;32(8):759-765. doi: 10.1177/0883073817705252. Epub 2017 May 3. J Child Neurol. 2017. PMID: 28464723 Free PMC article.
PRUNE1: a disease-causing gene for secondary microcephaly.
Karakaya M, Yilmaz S, Storbeck M, Hoelker I, Heller R, Serdaroglu G, Gökben S, Yis U, Wirth B. Karakaya M, et al. Among authors: yilmaz s. Brain. 2017 Oct 1;140(10):e61. doi: 10.1093/brain/awx197. Brain. 2017. PMID: 28969376 No abstract available.
2,799 results