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Journal Abstract Search

195 related items for PubMed ID: 8797533

  • 1. A point mutation associated with a severe phenotype of neurofibromatosis 2.
    MacCollin M, Braverman N, Viskochil D, Ruttledge M, Davis K, Ojemann R, Gusella J, Parry DM.
    Ann Neurol; 1996 Sep; 40(3):440-5. PubMed ID: 8797533
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic variability associated with 14 splice-site mutations in the NF2 gene.
    Kluwe L, MacCollin M, Tatagiba M, Thomas S, Hazim W, Haase W, Mautner VF.
    Am J Med Genet; 1998 May 18; 77(3):228-33. PubMed ID: 9605590
    [Abstract] [Full Text] [Related]

  • 3. Impairment of cell adhesion by expression of the mutant neurofibromatosis type 2 (NF2) genes which lack exons in the ERM-homology domain.
    Koga H, Araki N, Takeshima H, Nishi T, Hirota T, Kimura Y, Nakao M, Saya H.
    Oncogene; 1998 Aug 20; 17(7):801-10. PubMed ID: 9779996
    [Abstract] [Full Text] [Related]

  • 4. Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?
    Bruder CE, Ichimura K, Blennow E, Ikeuchi T, Yamaguchi T, Yuasa Y, Collins VP, Dumanski JP.
    Genes Chromosomes Cancer; 1999 Jun 20; 25(2):184-90. PubMed ID: 10338003
    [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 20; 77(2):163-70. PubMed ID: 19968670
    [Abstract] [Full Text] [Related]

  • 6. 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 20; 30(6):835-41. PubMed ID: 19704365
    [Abstract] [Full Text] [Related]

  • 7. [Neurofibromatosis type 2 (NF2)].
    Araki N, Takeshima H, Saya H.
    Gan To Kagaku Ryoho; 1997 Sep 20; 24(11):1427-31. PubMed ID: 9309136
    [Abstract] [Full Text] [Related]

  • 8. The neurofibromatosis 2 (NF2) tumour suppressor gene: implications beyond the hereditary tumour syndrome?
    Kley N, Seizinger BR.
    Cancer Surv; 1995 Sep 20; 25():207-18. PubMed ID: 8718520
    [Abstract] [Full Text] [Related]

  • 9. 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 20; 42(1):45-8. PubMed ID: 15635074
    [Abstract] [Full Text] [Related]

  • 10. Molecular characterization of germline NF2 gene rearrangements.
    Legoix P, Sarkissian HD, Cazes L, Giraud S, Sor F, Rouleau GA, Lenoir G, Thomas G, Zucman-Rossi J.
    Genomics; 2000 Apr 01; 65(1):62-6. PubMed ID: 10777666
    [Abstract] [Full Text] [Related]

  • 11. Clinical manifestations of mutations in the neurofibromatosis type 2 gene in vestibular schwannomas (acoustic neuromas).
    Welling DB.
    Laryngoscope; 1998 Feb 01; 108(2):178-89. PubMed ID: 9473065
    [Abstract] [Full Text] [Related]

  • 12. [Development and establishment of a yeast-based stop codon assay for detection of NF2 gene premature-terminating mutations].
    Kobayashi H.
    Hokkaido Igaku Zasshi; 1999 Sep 01; 74(5):377-86. PubMed ID: 10495852
    [Abstract] [Full Text] [Related]

  • 13. Phenotypic variability in monozygotic twins with neurofibromatosis 2.
    Baser ME, Ragge NK, Riccardi VM, Janus T, Gantz B, Pulst SM.
    Am J Med Genet; 1996 Sep 06; 64(4):563-7. PubMed ID: 8870923
    [Abstract] [Full Text] [Related]

  • 14. Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients.
    Ruggieri M, Iannetti P, Polizzi A, La Mantia I, Spalice A, Giliberto O, Platania N, Gabriele AL, Albanese V, Pavone L.
    Neuropediatrics; 2005 Feb 06; 36(1):21-34. PubMed ID: 15776319
    [Abstract] [Full Text] [Related]

  • 15. Somatic neurofibromatosis type 2 gene mutations and growth characteristics in vestibular schwannoma.
    Irving RM, Harada T, Moffat DA, Hardy DG, Whittaker JL, Xuereb JH, Maher ER.
    Am J Otol; 1997 Nov 06; 18(6):754-60. PubMed ID: 9391673
    [Abstract] [Full Text] [Related]

  • 16. Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.
    Bianchi AB, Hara T, Ramesh V, Gao J, Klein-Szanto AJ, Morin F, Menon AG, Trofatter JA, Gusella JF, Seizinger BR.
    Nat Genet; 1994 Feb 06; 6(2):185-92. PubMed ID: 8162073
    [Abstract] [Full Text] [Related]

  • 17. 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 06; 42(7):540-6. PubMed ID: 15994874
    [Abstract] [Full Text] [Related]

  • 18. Detection of novel NF2 mutations by an RNA mismatch cleavage method.
    Faudoa R, Xue Z, Lee F, Baser ME, Hung G.
    Hum Mutat; 2000 Jul 06; 15(5):474-8. PubMed ID: 10790209
    [Abstract] [Full Text] [Related]

  • 19. Expression of neurofibromatosis 2 transcript and gene product during mouse fetal development.
    Huynh DP, Tran TM, Nechiporuk T, Pulst SM.
    Cell Growth Differ; 1996 Nov 06; 7(11):1551-61. PubMed ID: 8930405
    [Abstract] [Full Text] [Related]

  • 20. Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas.
    Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM.
    Hum Mol Genet; 1994 Jun 06; 3(6):885-91. PubMed ID: 7951231
    [Abstract] [Full Text] [Related]

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