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Journal Abstract Search

231 related items for PubMed ID: 25725045

  • 1. Bilateral vestibular schwannomas in older patients: NF2 or chance?
    Evans DG, Freeman S, Gokhale C, Wallace A, Lloyd SK, Axon P, Ward CL, Rutherford S, King A, Huson SM, Ramsden RT, Manchester NF2 service.
    J Med Genet; 2015 Jun; 52(6):422-4. PubMed ID: 25725045
    [Abstract] [Full Text] [Related]

  • 2. Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas.
    Mohyuddin A, Neary WJ, Wallace A, Wu CL, Purcell S, Reid H, Ramsden RT, Read A, Black G, Evans DG.
    J Med Genet; 2002 May; 39(5):315-22. PubMed ID: 12011146
    [Abstract] [Full Text] [Related]

  • 3. Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas.
    Kluwe L, Mautner V, Heinrich B, Dezube R, Jacoby LB, Friedrich RE, MacCollin M.
    J Med Genet; 2003 Feb; 40(2):109-14. PubMed ID: 12566519
    [Abstract] [Full Text] [Related]

  • 4. Multiple meningiomas: differential involvement of the NF2 gene in children and adults.
    Evans DG, Watson C, King A, Wallace AJ, Baser ME.
    J Med Genet; 2005 Jan; 42(1):45-8. PubMed ID: 15635074
    [Abstract] [Full Text] [Related]

  • 5. [Neurofibromatosis type 2 (central neurofibromatosis or bilateral acoustic neuromas, vestibular schwannomas): from phenotype to gene].
    Sabol Z, Kipke-Sabol L, Miklić P, Hajnsek-Propadalo S, Sabol F.
    Lijec Vjesn; 2006 Jan; 128(9-10):309-16. PubMed ID: 17128670
    [Abstract] [Full Text] [Related]

  • 6. NF2 genetic alterations in sporadic vestibular schwannomas: clinical implications.
    Lassaletta L, Torres-Martín M, Peña-Granero C, Roda JM, Santa-Cruz-Ruiz S, Castresana JS, Gavilan J, Rey JA.
    Otol Neurotol; 2013 Sep; 34(7):1355-61. PubMed ID: 23921927
    [Abstract] [Full Text] [Related]

  • 7. Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma.
    Irving RM, Moffat DA, Hardy DG, Barton DE, Xuereb JH, Maher ER.
    Hum Mol Genet; 1994 Feb; 3(2):347-50. PubMed ID: 8004107
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  • 8. Unilateral vestibular schwannoma with other neurofibromatosis type 2-related tumors: clinical and molecular study of a unique phenotype.
    Aghi M, Kluwe L, Webster MT, Jacoby LB, Barker FG, Ojemann RG, Mautner VF, MacCollin M.
    J Neurosurg; 2006 Feb; 104(2):201-7. PubMed ID: 16509493
    [Abstract] [Full Text] [Related]

  • 9. Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation.
    Warren C, James LA, Ramsden RT, Wallace A, Baser ME, Varley JM, Evans DG.
    J Med Genet; 2003 Nov; 40(11):802-6. PubMed ID: 14627667
    [Abstract] [Full Text] [Related]

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  • 15. Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas.
    Wu CL, Thakker N, Neary W, Black G, Lye R, Ramsden RT, Read AP, Evans DG.
    J Med Genet; 1998 Dec; 35(12):973-7. PubMed ID: 9863591
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  • 16. Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?
    Evans DG, Ramsden RT, Gokhale C, Bowers N, Huson SM, Wallace A.
    Clin Genet; 2007 Apr; 71(4):354-8. PubMed ID: 17470137
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  • 17. Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomas.
    Hadfield KD, Smith MJ, Urquhart JE, Wallace AJ, Bowers NL, King AT, Rutherford SA, Trump D, Newman WG, Evans DG.
    Oncogene; 2010 Nov 25; 29(47):6216-21. PubMed ID: 20729918
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  • 18. Mutations and allelic loss of the NF2 gene in neurofibromatosis 2-associated skin tumors.
    Kluwe L, Friedrich RE, Hagel C, Lindenau M, Mautner VF.
    J Invest Dermatol; 2000 May 25; 114(5):1017-21. PubMed ID: 10771486
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  • 19. Neurofibromatosis type 2.
    Evans GR, Lloyd SKW, Ramsden RT.
    Adv Otorhinolaryngol; 2011 May 25; 70():91-98. PubMed ID: 21358190
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