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Journal Abstract Search

123 related items for PubMed ID: 8870923

  • 1. 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]

  • 2. 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 06; 25(2):184-90. PubMed ID: 10338003
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [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 May 18; 128(9-10):309-16. PubMed ID: 17128670
    [Abstract] [Full Text] [Related]

  • 5. 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 18; 40(3):440-5. PubMed ID: 8797533
    [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 18; 30(6):835-41. PubMed ID: 19704365
    [Abstract] [Full Text] [Related]

  • 7. Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity.
    Parry DM, Eldridge R, Kaiser-Kupfer MI, Bouzas EA, Pikus A, Patronas N.
    Am J Med Genet; 1994 Oct 01; 52(4):450-61. PubMed ID: 7747758
    [Abstract] [Full Text] [Related]

  • 8. Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2).
    Zhao Y, Kumar RA, Baser ME, Evans DG, Wallace A, Kluwe L, Mautner VF, Parry DM, Rouleau GA, Joe H, Friedman JM.
    Genet Epidemiol; 2002 Oct 01; 23(3):245-59. PubMed ID: 12384977
    [Abstract] [Full Text] [Related]

  • 9. Neurofibromatosis type 2 in an infant with multiple plexiform schwannomas as first symptom.
    Miyakawa T, Kamada N, Kobayashi T, Hirano K, Fujii K, Sasahara Y, Nagai Y, Shinkai H.
    J Dermatol; 2007 Jan 01; 34(1):60-4. PubMed ID: 17204104
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 77(2):163-70. PubMed ID: 19968670
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 36(1):21-34. PubMed ID: 15776319
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. [Neurofibromatosis type 2 (NF2)].
    Araki N, Takeshima H, Saya H.
    Gan To Kagaku Ryoho; 1997 Sep 01; 24(11):1427-31. PubMed ID: 9309136
    [Abstract] [Full Text] [Related]

  • 14. Influence of genes and environment on brain volumes in twin pairs concordant and discordant for bipolar disorder.
    van der Schot AC, Vonk R, Brans RG, van Haren NE, Koolschijn PC, Nuboer V, Schnack HG, van Baal GC, Boomsma DI, Nolen WA, Hulshoff Pol HE, Kahn RS.
    Arch Gen Psychiatry; 2009 Feb 01; 66(2):142-51. PubMed ID: 19188536
    [Abstract] [Full Text] [Related]

  • 15. Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma.
    Zirn B, Arning L, Bartels I, Shoukier M, Hoffjan S, Neubauer B, Hahn A.
    Clin Genet; 2012 Jan 01; 81(1):82-7. PubMed ID: 21175598
    [Abstract] [Full Text] [Related]

  • 16. Neurofibromatosis type 2: a new mechanism of tumor suppression.
    Lutchman M, Rouleau GA.
    Trends Neurosci; 1996 Sep 01; 19(9):373-7. PubMed ID: 8873351
    [Abstract] [Full Text] [Related]

  • 17. Two pairs of proven monozygotic twins discordant for familial amyloid neuropathy (FAP) TTR Met 30.
    Munar-Qués M, Pedrosa JL, Coelho T, Gusmão L, Seruca R, Amorim A, Sequeiros J.
    J Med Genet; 1999 Aug 01; 36(8):629-32. PubMed ID: 10465115
    [Abstract] [Full Text] [Related]

  • 18. Neurofibromatosis type 2 discordance in monozygous twins.
    Amico S, Smith P, Tobi S, Perry M, Wallace A, Evans DG.
    Fam Cancer; 2020 Jan 01; 19(1):37-40. PubMed ID: 31965447
    [Abstract] [Full Text] [Related]

  • 19. Neurofibromatosis type 2: genetic and clinical features.
    Evans DG.
    Ear Nose Throat J; 1999 Feb 01; 78(2):97-100. PubMed ID: 10089694
    [Abstract] [Full Text] [Related]

  • 20. [Type 2 neurofibromatosis without acoustic neuroma].
    Mautner VF, Lindenau M, Köppen J, Hazim W, Kluwe L.
    Zentralbl Neurochir; 1995 Feb 01; 56(2):83-7. PubMed ID: 7639047
    [Abstract] [Full Text] [Related]

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