Showing results (441-450 of 466) with videos related to
Sort By:
Pageof 47
Neuro-Oncology|November 3, 2018
Inflammation and vascular permeability correlate with growth in sporadic vestibular schwannomaDaniel Lewis, Federico Roncaroli, Erjon Agushi, et al.Journal of Medical Genetics|June 25, 2015
Multiple synchronous sites of origin of vestibular schwannomas in neurofibromatosis Type 2Stavros M Stivaros, Anat O Stemmer-Rachamimov, Robert Alston, et al.Journal of Neurosurgery|May 30, 2020
The microenvironment in sporadic and neurofibromatosis type II-related vestibular schwannoma: the same tumor or different? A comparative imaging and neuropathology studyDaniel Lewis, Carmine A Donofrio, Claire O'Leary, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2018
Schwannomatosis: a genetic and epidemiological studyD Gareth Evans, Naomi L Bowers, Simon Tobi, et al.Journal of Medical Genetics|August 29, 2024
Genetic findings in people with schwannomas who do not meet clinical diagnostic criteria for NF2-related schwannomatosisMiriam J Smith, Cristina Perez-Becerril, Mwee van der Meer, et al.Cerebral Cortex (New York, N.Y. : 1991)|April 20, 2020
Heterogeneity in Brain Microstructural Development Following Preterm BirthRalica Dimitrova, Maximilian Pietsch, Daan Christiaens, et al.AJNR. American Journal of Neuroradiology|October 22, 2021
A Uniform Description of Perioperative Brain MRI Findings in Infants with Severe Congenital Heart Disease: Results of a European CollaborationR Stegeman, M Feldmann, N H P Claessens, et al.Neuroimage|June 12, 2018
Construction of a neonatal cortical surface atlas using Multimodal Surface Matching in the Developing Human Connectome ProjectJelena Bozek, Antonios Makropoulos, Andreas Schuh, et al.American Journal of Human Genetics|October 23, 2012
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing lossSimon von Ameln, Geng Wang, Redouane Boulouiz, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Identifying the deficiencies of current diagnostic criteria for neurofibromatosis 2 using databases of 2777 individuals with molecular testingD Gareth Evans, Andrew T King, Naomi L Bowers, et al.Pageof 47