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Journal of Neurosurgery|December 25, 2007
A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigationKaya Bilguvar, Mohamad Bydon, Fatih Bayrakli, et al.Neurosurgical Focus|November 2, 2016
Cerebrospinal fluid hypersecretion in pediatric hydrocephalusJason K Karimy, Daniel Duran, Jamie K Hu, et al.Frontiers in Neurology|August 10, 2017
Malignant Cerebellar Edema Subsequent to Accidental Prescription Opioid Intoxication in ChildrenDaniel Duran, Robert D Messina, Lauren A Beslow, et al.Journal of Neurosurgery. Pediatrics|October 27, 2023
Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosisEmre Kiziltug, Phan Q Duy, Garrett Allington, et al.Cold Spring Harbor Molecular Case Studies|June 16, 2018
De novo MYH9 mutation in congenital scalp hemangiomaElena I Fomchenko, Daniel Duran, Sheng Chih Jin, et al.Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.Journal of Neurosurgery. Pediatrics|October 27, 2019
Genomic alterations underlying spinal metastases in pediatric H3K27M-mutant pineal parenchymal tumor of intermediate differentiation: case reportElena I Fomchenko, E Zeynep Erson-Omay, Adam J Kundishora, et al.Neurogenetics|January 19, 2010
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophyLuis E Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, et al.Acute and Critical Care|March 28, 2023
Use of droxidopa for blood pressure augmentation after acute spinal cord injury: case reportsChristopher S Hong, Muhammad K Effendi, Abdalla A Ammar, et al.NPJ Genomic Medicine|June 13, 2020
Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastomaChristopher S Hong, Juan C Vasquez, Adam J Kundishora, et al.Pageof 7