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Turkish Neurosurgery|February 6, 2020
Transforaminal Epidural Steroid Injection in the Treatment of Pain in Foraminal and Paramedian Lumbar Disc HerniationsBulent Guclu, Levent Deniz, Yucel Yuce, et al.Turkish Neurosurgery|January 9, 2023
AGR2 Gene Expression in Glioblastoma: A Novel Molecular Potential Target for Diagnosis and TreatmentHuseyin Utku Adilay, Sevket Evran, Salim Katar, et al.American Journal of Human Genetics|November 13, 2004
Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13Brian V Nahed, Askin Seker, Bulent Guclu, et al.Stroke|February 25, 2006
Molecular genetic analysis of two large kindreds with intracranial aneurysms demonstrates linkage to 11q24-25 and 14q23-31Ali K Ozturk, Brian V Nahed, Mohamad Bydon, et al.BMC Genetics|October 1, 2013
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtypeFatih Bayrakli, Bulent Guclu, Cengiz Yakicier, et al.Pediatric Neurology|December 3, 2014
Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutationsAhmet Okay Caglayan, Jacob F Baranoski, Fesih Aktar, et al.Neuron|July 10, 2018
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital HydrocephalusCharuta Gavankar Furey, Jungmin Choi, Sheng Chih Jin, et al.Nature Medicine|October 20, 2020
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalusSheng Chih Jin, Weilai Dong, Adam J Kundishora, et al.Pageof 4