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Clinical Genetics|February 10, 2023
Updated protocol for genetic testing, screening and clinical management of individuals at risk of NF2-related schwannomatosisDorothy Halliday, Beatrice Emmanouil, D Gareth R Evans
The Journal of Laryngology and Otology|January 17, 2024
A force sensor improves trainee technique for rigid endoscopySumrit Bola, Manu Kunaal Shrivastava, Josh Brown, et al.
Ophthalmic Research|October 21, 2021
Structural Abnormalities of the Central Retina in Neurofibromatosis Type 2Beatrice Emmanouil, Martin Wasik, Peter Charbel Issa, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|June 21, 2018
Neurofibromatosis Type 2-Related Eye Disease Correlated With Genetic Severity TypeSally L Painter, Zuzana Sipkova, Beatrice Emmanouil, et al.
The Laryngoscope|November 20, 2023
Stereotactic Radiosurgery and Radiotherapy for Vestibular Schwannoma in NF2-Related SchwannomatosisManu Shrivastava, Beatrice Emmanouil, Rajeev Mathew, et al.
Journal of Chemical Theory and Computation|November 19, 2015
Sidekick for Membrane Simulations: Automated Ensemble Molecular Dynamics Simulations of Transmembrane HelicesBenjamin A Hall, Khairul Bariyyah Abd Halim, Amanda Buyan, et al.
Journal of Medical Genetics|August 30, 2017
Genetic Severity Score predicts clinical phenotype in NF2Dorothy Halliday, Beatrice Emmanouil, Pieter Pretorius, et al.
The Laryngoscope|November 21, 2018
Progression of hearing loss in neurofibromatosis type 2 according to genetic severityBeatrice Emmanouil, Rory Houston, Anne May, et al.
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