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Current Opinion in Oncology, ISSN 1040-8746, 08/2019
PURPOSE OF REVIEWNeurofibromatosis type 2 (NF2) is a schwannoma predisposition syndrome, alongside schwannomatosis related to germline LZTR1 and SMARCB1... 
Journal Article
Pediatrics, ISSN 0031-4005, 01/2009, Volume 123, Issue 1, pp. 391 - 398
Journal Article
Journal Article
The Laryngoscope, ISSN 0023-852X, 04/2019, Volume 129, Issue 4, pp. 974 - 980
Journal Article
Disability and Rehabilitation, ISSN 0963-8288, 07/2019, Volume 41, Issue 14, pp. 1632 - 1638
Purpose: Patients with Neurofibromatosis type 2 often experience debilitating neuro-otological problems which affect their mobility and balance. This study... 
genetic severity | dynamic gait index | Neurofibromatosis type 2 | vestibular rehabilitation | RELIABILITY | DIZZINESS | PREVALENCE | BALANCE DISORDERS | INDIVIDUALS | HYPOFUNCTION | VERSION | REHABILITATION | QUALITY-OF-LIFE | VALIDITY
Journal Article
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 11/2018, Volume 89, Issue 11, pp. 1215 - 1219
ObjectivesSchwannomatosis is a dominantly inherited condition predisposing to schwannomas of mainly spinal and peripheral nerves with some diagnostic overlap... 
schwannomatosis | SMARCB1 | LZTR1 | vestibular schwannoma | SURGERY | EXCLUSION | PSYCHIATRY | MUTATION | TUMOR-SUPPRESSOR GENE | NF2 | PREVALENCE | DIAGNOSTIC-CRITERIA | VESTIBULAR SCHWANNOMAS | CLINICAL NEUROLOGY | TYPE-2 NEUROFIBROMATOSIS | Calcification | Neurology | Population | Family medical history | Mutation
Journal Article
by Hexter, Adam and Jones, Adrian and Joe, Harry and Heap, Laura and Smith, Miriam J and Wallace, Andrew J and Halliday, Dorothy and Parry, Allyson and Taylor, Amy and Raymond, Lucy and Shaw, Adam and Afridi, Shazia and Obholzer, Rupert and Axon, Patrick and King, Andrew T and Friedman, Jan M and D Gareth R, Gareth R and Burnet, Neil and Donnelly, Neil and Durie-Gair, Juliette and English, Martin and Folland, Nicola and Foweraker, Karen and Harris, Fiona and Harris, Frances and Heney, David and Jeffries, Sarah and Jena, Raj and Knight, Richard and Lamb, Tamara and Macfarlane, Robert and Mannion, Richard and Nicholson, James and Price, Richard and Rands, Ella and Sanghera, Paul and Scoffings, Daniel and Tysome, James and Ferner, Rosalie E and Hammond, Chris and Lascelles, Karine and Nunn, Terry and Saeed, Shakeel and Swampillai, Angela and Thomson, Suki and Walsh, Daniel and Williams, Victoria and Wood, Sue and Anup, Raji and Duff, Chris and Evans, D Gareth and Freeman, Simon R and Howie, Emma and Huson, Susan M and Jarvis, Nicola and Kamaly-Asi, Ian and King, Andrew and Kellett, Mark and Kilday, John-Paul and Lloyd, Simon K and Malluci, Connor and Mawman, Deborah and McBain, Catherine and Mills, Sam and O'Driscoll, Martin and Patel, Sonia and Perry, Mary and Rutherford, Scott A and Scott-Kitching, Vilka and Stivaros, Stavros M and Thomas, Owen and Vassallo, Grace and Ward, Charlotte L and Blesing, Claire and Cogswell, Lucy and Dalton, Louise and Dodridge, Caroline and Elston, John and Giele, Henk and Hanemann, C Oliver and Howard, Wendy and Johnson, David and Kerr, Richard and Laws, Avianna and Lee, James and Mace, Elle and May, Anne and Milford, Chris and Pretorius, Peter and Ramsden, James and Redman, Caroline and Warner, Nicola and Wilson, Shaun and English Specialist NF2 Res Grp and English Specialist NF2 Research Group and The English Specialist NF2 Research Group
Journal of Medical Genetics, ISSN 0022-2593, 08/2015, Volume 52, Issue 10, pp. 699 - 705
Journal Article
Archives of Disease in Childhood, ISSN 0003-9888, 05/2018, Volume 103, Issue 5, pp. 463 - 469
Journal Article
by Palles, Claire and Cazier, Jean-Baptiste and Howarth, Kimberley M and Domingo, Enric and Jones, Angela M and Broderick, Peter and Kemp, Zoe and Spain, Sarah L and Almeida, Estrella Guarino and Salguero, Israel and Sherborne, Amy and Chubb, Daniel and Carvajal-Carmona, Luis G and Ma, Yusanne and Kaur, Kulvinder and Dobbins, Sara and Barclay, Ella and Gorman, Maggie and Martin, Lynn and Kovac, Michal B and Humphray, Sean and Lucassen, Anneke and Holmes, Christopher H and Bentley, David and Donnelly, Peter and Taylor, Jenny and Petridis, Christos and Roylance, Rebecca and Sawyer, Elinor J and Kerr, David J and Clark, Susan and Grimes, Jonathan and Kearsey, Stephen E and Thomas, Huw J.W and McVean, Gilean and Houlston, Richard S and Tomlinson, Ian and Thomas, Huw J.W and Maher, Eamonn and Evans, Gareth and Cummings, Carole and Stevens, Margaret and Walker, Lisa and Halliday, Dorothy and Armstrong, Ruth and Paterson, Joan and Hodgson, Shirley and Homfray, Tessa and Side, Lucy and Izatt, Louise and Donaldson, Alan and Tomkins, Susan and Morrison, Patrick and Goodman, Selina and Brewer, Carole and Henderson, Alex and Davidson, Rosemarie and Murday, Victoria and Cook, Jaqueline and Haites, Nneva and Bishop, Timothy and Sheridan, Eamonn and Green, Andrew and Marks, Christopher and Carpenter, Sue and Broughton, Mary and Greenhalge, Lynn and Suri, Mohnish and Bell, John and Ratcliffe, Peter and Wilkie, Andrew and Broxholme, John and Buck, David and Cornall, Richard and Gregory, Lorna and Knight, Julian and Lunter, Gerton and Kingsbury, Zoya and Grocock, Russell and Hatton, Edouard and Holmes, Christopher C and Hughes, Linda and Humburg, Peter and Kanapin, Alexander and Murray, Lisa and Rimmer, Andy and WGS500 Consortium and CORGI Consortium and The WGS500 Consortium and The CORGI Consortium
Nature Genetics, ISSN 1061-4036, 02/2013, Volume 45, Issue 2, pp. 136 - 143
Journal Article