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Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants.
Hazan F, Gürsoy S, Unalp A, Yılmaz U, Demirağ B, Aydin Köker S, Ozyılmaz B, Erdogan KM, Kalenderer Ö, Erkuş S, Gürçınar M, Tükün A. Hazan F, et al. Among authors: aydin koker s. Neurol Sci. 2021 May;42(5):2045-2057. doi: 10.1007/s10072-020-04988-0. Epub 2021 Jan 14. Neurol Sci. 2021. PMID: 33443663
Successful Management of l-Asparaginase-Associated Pancreatitis With Octreotide and Pegylated Asparaginase in 2 Patients With Acute Lymphoblastic Leukemia: Is There a Different Rare Warning Sign of Hypoglycemia for l-Asparaginase-Associated Pancreatitis?
Aydin Köker S, Oymak Y, Demirağ B, Karapinar TH, Koker A, Genç S, Erdemir G, Vergin RC. Aydin Köker S, et al. Clin Ther. 2020 Apr;42(4):e82-e86. doi: 10.1016/j.clinthera.2020.02.015. Epub 2020 Mar 14. Clin Ther. 2020. PMID: 32184014
Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia.
Aydin Koker S, Karapinar TH, Oymak Y, Bianchi P, Fermo E, Gozmen S, Vergin C. Aydin Koker S, et al. J Pediatr Hematol Oncol. 2018 Oct;40(7):e421-e423. doi: 10.1097/MPH.0000000000001207. J Pediatr Hematol Oncol. 2018. PMID: 29846281
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