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Archives of Disease in Childhood|March 15, 2018
Diagnosis of sporadic neurofibromatosis type 2 in the paediatric populationGeetha Anand, Grace Vasallo, Maria Spanou, et al.Journal of Medical Genetics|February 1, 2011
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onsetMiriam J Smith, Jenny E Higgs, Naomi L Bowers, et al.Journal of Medical Genetics|August 16, 2015
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patientsAdam Hexter, Adrian Jones, Harry Joe, et al.Journal of Medical Genetics|June 25, 2020
Sporadic vestibular schwannoma: a molecular testing summaryKatherine V Sadler, Naomi L Bowers, Claire Hartley, et al.Neurosurgery|October 4, 2017
Malignant Peripheral Nerve Sheath Tumors are not a Feature of Neurofibromatosis Type 2 in the Unirradiated PatientAndrew T King, Scott A Rutherford, Charlotte Hammerbeck-Ward, et al.Neurology|December 7, 2014
Mutations in LZTR1 add to the complex heterogeneity of schwannomatosisMiriam J Smith, Bertand Isidor, Christian Beetz, et al.Journal of Medical Genetics|June 26, 2024
NF2-related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological studyClaire Forde, Miriam J Smith, George J Burghel, 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.British Journal of Cancer|February 20, 2022
Evaluation of tumour surveillance protocols and outcomes in von Hippel-Lindau disease in a national health serviceEamonn R Maher, Julian Adlard, Julian Barwell, et al.Pageof 4