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Journal Abstract Search

202 related items for PubMed ID: 7747758

  • 1.
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  • 2. 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; 36(1):21-34. PubMed ID: 15776319
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  • 3. Distribution of nonvestibular cranial nerve schwannomas in neurofibromatosis 2.
    Fisher LM, Doherty JK, Lev MH, Slattery WH.
    Otol Neurotol; 2007 Dec; 28(8):1083-90. PubMed ID: 18043434
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  • 4. 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
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  • 6. 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
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  • 7. 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 18; 34(1):60-4. PubMed ID: 17204104
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  • 11. Skin abnormalities in neurofibromatosis 2.
    Mautner VF, Lindenau M, Baser ME, Kluwe L, Gottschalk J.
    Arch Dermatol; 1997 Dec 18; 133(12):1539-43. PubMed ID: 9420538
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  • 12. Characterization of early onset neurofibromatosis type 2.
    Matsuo M, Ohno K, Ohtsuka F.
    Brain Dev; 2014 Feb 18; 36(2):148-52. PubMed ID: 23414620
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  • 13. 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 18; 42(1):45-8. PubMed ID: 15635074
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  • 14. Infratentorial meningioma in an 8-year-old child as first sign of neurofibromatosis type 2.
    Stettner GM, Rostasy KM, Ludwig HC, Merkler D, Fahsold R, Gärtner J.
    Neuropediatrics; 2007 Feb 18; 38(1):29-31. PubMed ID: 17607601
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  • 15. Combined retinal hamartomas leading to the diagnosis of neurofibromatosis type 2.
    Grant EA, Trzupek KM, Reiss J, Crow K, Messiaen L, Weleber RG.
    Ophthalmic Genet; 2008 Sep 18; 29(3):133-8. PubMed ID: 18766994
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  • 16. Prognostic value and management of spinal tumors in neurofibromatosis type 2 patients.
    Aboukais R, Baroncini M, Zairi F, Bonne NX, Schapira S, Vincent C, Lejeune JP.
    Acta Neurochir (Wien); 2013 May 18; 155(5):771-7. PubMed ID: 23381342
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  • 17. The ocular presentation of neurofibromatosis 2.
    Ragge NK, Baser ME, Riccardi VM, Falk RE.
    Eye (Lond); 1997 May 18; 11 ( Pt 1)():12-8. PubMed ID: 9246269
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  • 18. 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
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  • 19. 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
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  • 20. Neurofibromatosis.
    Roos KL, Muckway M.
    Dermatol Clin; 1995 Jan 18; 13(1):105-11. PubMed ID: 7712636
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