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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2021
A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-SaguenayBedia Samanci, Ebru Erzurumluoglu Gokalp, Basar Bilgic, et al.Turkish Neurosurgery|June 2, 2026
Downregulation of miR-221, miR-143, and miR-22 in Meningioma: Diagnostic Performance in a Single-Center Case-Control StudySalim Tekir, Emre Ozkara, Ebru Erzurumluoglu, et al.International Journal of Ophthalmology|June 21, 2021
Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, TurkeyNadir Unlu, Ebru Erzurumluoglu Gokalp, Serap Arslan, et al.Cancer Genetics|March 27, 2021
A new four-way complex translocation variant involving the t(8;5;21;4)(q21;q13,q22,q31) and the relocalization of AML1/ETO fusion geneSevgi Isik, Hava Uskudar Teke, Gulcin Gunden, et al.American Journal of Medical Genetics. Part A|January 21, 2020
A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiencyHasan Bas, Oguz Cilingir, Neslihan Tekin, et al.American Journal of Medical Genetics. Part A|September 25, 2021
NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephalyHasan Bas, Suzan Saylisoy, Oguz Cilingir, et al.Biomedicines|May 27, 2026
Aquaporin-4 and MicroRNA Expression in Meningiomas: A Tissue-Level Exploratory AnalysisHuseyin Omer Keskin, Emre Ozkara, Ebru Erzurumluoglu, et al.Journal of Korean Neurosurgical Society|February 3, 2025
The Role of miRNA Expression Profiles in Different Biofluids İn Aneurysm RuptureSara Khadem Ansari, Ebru Erzurumluoglu Gokalp, Emre Ozkara, et al.Cancer Genetics|July 5, 2021
A pediatric BAL case with double Ph chromosomes and trisomy 5Gulcin Gunden, Sevgi Isik, Canan Ozdemir, et al.Neurobiology of Aging|January 28, 2019
The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degenerationEbru Erzurumluoglu, Oguz Cilingir, Belgin Demet Ozbabalik Adapinar, et al.Pageof 3