BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 28848060)

  • 1. Genetic Severity Score predicts clinical phenotype in NF2.
    Halliday D; Emmanouil B; Pretorius P; MacKeith S; Painter S; Tomkins H; Evans DG; Parry A
    J Med Genet; 2017 Oct; 54(10):657-664. PubMed ID: 28848060
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severity.
    Halliday D; Emmanouil B; Vassallo G; Lascelles K; Nicholson J; Chandratre S; Anand G; Wasik M; Pretorius P; Evans DG; Parry A;
    Clin Genet; 2019 Aug; 96(2):151-162. PubMed ID: 30993672
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Phenotype-genotype study in 154 French NF2 mutation carriers].
    Demange L; De Moncuit C; Thomas G; Olschwang S
    Rev Neurol (Paris); 2007 Nov; 163(11):1031-8. PubMed ID: 18033041
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical manifestations of mutations in the neurofibromatosis type 2 gene in vestibular schwannomas (acoustic neuromas).
    Welling DB
    Laryngoscope; 1998 Feb; 108(2):178-89. PubMed ID: 9473065
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Further genotype--phenotype correlations in neurofibromatosis 2.
    Selvanathan SK; Shenton A; Ferner R; Wallace AJ; Huson SM; Ramsden RT; Evans DG
    Clin Genet; 2010 Feb; 77(2):163-70. PubMed ID: 19968670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neurofibromatosis type 2 (NF2): a clinical and molecular review.
    Evans DG
    Orphanet J Rare Dis; 2009 Jun; 4():16. PubMed ID: 19545378
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Predictors of vestibular schwannoma growth in patients with neurofibromatosis Type 2.
    Baser ME; Makariou EV; Parry DM
    J Neurosurg; 2002 Feb; 96(2):217-22. PubMed ID: 11838793
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.
    Evans DG; Trueman L; Wallace A; Collins S; Strachan T
    J Med Genet; 1998 Jun; 35(6):450-5. PubMed ID: 9643284
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients.
    Hexter A; Jones A; Joe H; Heap L; Smith MJ; Wallace AJ; Halliday D; Parry A; Taylor A; Raymond L; Shaw A; Afridi S; Obholzer R; Axon P; King AT; ; Friedman JM; Evans DG
    J Med Genet; 2015 Oct; 52(10):699-705. PubMed ID: 26275417
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neurofibromatosis type 2 (NF2): diagnosis and management.
    Lloyd SK; Evans DG
    Handb Clin Neurol; 2013; 115():957-67. PubMed ID: 23931824
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Concordance of bilateral vestibular schwannoma growth and hearing changes in neurofibromatosis 2: neurofibromatosis 2 natural history consortium.
    Fisher LM; Doherty JK; Lev MH; Slattery WH
    Otol Neurotol; 2009 Sep; 30(6):835-41. PubMed ID: 19704365
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progression of hearing loss in neurofibromatosis type 2 according to genetic severity.
    Emmanouil B; Houston R; May A; Ramsden JD; Hanemann CO; Halliday D; Parry A; Mackeith S
    Laryngoscope; 2019 Apr; 129(4):974-980. PubMed ID: 30456886
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2.
    Baser ME; Kuramoto L; Woods R; Joe H; Friedman JM; Wallace AJ; Ramsden RT; Olschwang S; Bijlsma E; Kalamarides M; Papi L; Kato R; Carroll J; Lázaro C; Joncourt F; Parry DM; Rouleau GA; Evans DG
    J Med Genet; 2005 Jul; 42(7):540-6. PubMed ID: 15994874
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2.
    Teranishi Y; Miyawaki S; Hongo H; Dofuku S; Okano A; Takayanagi S; Ota T; Yoshimura J; Qu W; Mitsui J; Nakatomi H; Morishita S; Tsuji S; Saito N
    J Med Genet; 2021 Oct; 58(10):701-711. PubMed ID: 33067351
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Vestibular schwannoma growth in patients with neurofibromatosis Type 2: a longitudinal study.
    Mautner VF; Baser ME; Thakkar SD; Feigen UM; Friedman JM; Kluwe L
    J Neurosurg; 2002 Feb; 96(2):223-8. PubMed ID: 11838794
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypes.
    Kluwe L; Bayer S; Baser ME; Hazim W; Haase W; Fünsterer C; Mautner VF
    Hum Genet; 1996 Nov; 98(5):534-8. PubMed ID: 8882871
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.
    Parry DM; MacCollin MM; Kaiser-Kupfer MI; Pulaski K; Nicholson HS; Bolesta M; Eldridge R; Gusella JF
    Am J Hum Genet; 1996 Sep; 59(3):529-39. PubMed ID: 8751853
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neurofibromatosis type 2.
    Slattery WH
    Otolaryngol Clin North Am; 2015 Jun; 48(3):443-60. PubMed ID: 26043141
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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 onset.
    Smith MJ; Higgs JE; Bowers NL; Halliday D; Paterson J; Gillespie J; Huson SM; Freeman SR; Lloyd S; Rutherford SA; King AT; Wallace AJ; Ramsden RT; Evans DG
    J Med Genet; 2011 Apr; 48(4):261-5. PubMed ID: 21278391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical course of vestibular schwannoma in pediatric neurofibromatosis Type 2.
    Choi JW; Lee JY; Phi JH; Wang KC; Chung HT; Paek SH; Kim DG; Park SH; Kim SK
    J Neurosurg Pediatr; 2014 Jun; 13(6):650-7. PubMed ID: 24724714
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.