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Neurosurgery|February 2, 2023
Increased Circulating Chemokines and Macrophage Recruitment in Growing Vestibular SchwannomasCathal John Hannan, Daniel Lewis, Claire O'Leary, et al.Neuro-Oncology|December 18, 2020
Disease course of neurofibromatosis type 2: a 30-year follow-up study of 353 patients seen at a single institutionClaire Forde, Andrew T King, Scott A Rutherford, et al.Brain : a Journal of Neurology|December 22, 2022
Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21Katherine V Sadler, John Bowes, Charlie F Rowlands, et al.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.Journal of Neurosurgery|March 18, 2023
Intraoperative diagnosis of facial schwannomas: a multicenter summation of clinical experience, preoperative avoidance, and intraoperative management protocolDaniel Lewis, Cathal John Hannan, Aaron R Plitt, 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 6