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Familial Cancer|November 25, 2025
The clinical spectrum of paediatric NF2- related schwannomatosisDorothy Halliday, Lucy Hanington
Current Opinion in Oncology|August 20, 2019
Neurofibromatosis type 2 and related disordersDorothy Halliday, Allyson Parry, D Gareth Evans
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
Developmental Medicine and Child Neurology|September 15, 2009
A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorderMichael Absoud, Jeremy R Parr, Dorothy Halliday, 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.
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