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Volumn 18, Issue 10, 2003, Pages 718-724

Neurofibromatosis 2 in the pediatric population

Author keywords

[No Author keywords available]

Indexed keywords

ACOUSTIC NEURINOMA; CLINICAL EXAMINATION; CONTROLLED STUDY; CRANIAL NEUROPATHY; DIAGNOSTIC PROCEDURE; FAMILY HISTORY; GENETIC ANALYSIS; HEARING IMPAIRMENT; HEARING LOSS; HISTOPATHOLOGY; HUMAN; IMAGE ANALYSIS; MAJOR CLINICAL STUDY; MEDICAL RECORD; MENINGIOMA; MOBILIZATION; NEUROFIBROMATOSIS; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; REVIEW; SPINAL CORD TUMOR; SURGICAL TECHNIQUE; TUMOR VOLUME; VISUAL IMPAIRMENT;

EID: 0242708725     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/08830738030180101301     Document Type: Review
Times cited : (67)

References (20)
  • 1
    • 0025455386 scopus 로고
    • NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update
    • Mulvihill JJ, Parry DM, Sherman JL, et al: NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update. Ann Intern Med 1990;113:39-52.
    • (1990) Ann. Intern. Med. , vol.113 , pp. 39-52
    • Mulvihill, J.J.1    Parry, D.M.2    Sherman, J.L.3
  • 2
    • 0037058777 scopus 로고    scopus 로고
    • Evaluation of clinical diagnostic criteria for neurofibromatosis 2
    • Baser ME, Friedman JM, Wallace AJ, et al: Evaluation of clinical diagnostic criteria for neurofibromatosis 2. Neurology 2002;59: 1759-1765.
    • (2002) Neurology , vol.59 , pp. 1759-1765
    • Baser, M.E.1    Friedman, J.M.2    Wallace, A.J.3
  • 3
    • 0026746684 scopus 로고
    • A clinical study of type 2 neurofibromatosis
    • Evans DGR, Huson SM, Donnai D, et al: A clinical study of type 2 neurofibromatosis. QJM 1992;84:603-618.
    • (1992) QJM , vol.84 , pp. 603-618
    • Evans, D.G.R.1    Huson, S.M.2    Donnai, D.3
  • 4
    • 0027937181 scopus 로고
    • Neurofibromatosis 2 (NF2): Clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity
    • Parry DM, Eldridge R, Kaiser-Kupfer MI, et al: Neurofibromatosis 2 (NF2): Clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity. Am J Med Genet 1994;52: 450-461.
    • (1994) Am. J. Med. Genet. , vol.52 , pp. 450-461
    • Parry, D.M.1    Eldridge, R.2    Kaiser-Kupfer, M.I.3
  • 5
    • 0029981434 scopus 로고    scopus 로고
    • The neuroimaging and clinical spectrum of neurofibromatosis 2
    • Mautner VF, Lindenau M, Baser ME, et al: The neuroimaging and clinical spectrum of neurofibromatosis 2. Neurosurgery 1996; 38:880-886.
    • (1996) Neurosurgery , vol.38 , pp. 880-886
    • Mautner, V.F.1    Lindenau, M.2    Baser, M.E.3
  • 6
    • 0032421712 scopus 로고    scopus 로고
    • The diagnosis and management of neurofibromatosis 2 in childhood
    • MacCollin M, Mautner VF: The diagnosis and management of neurofibromatosis 2 in childhood. Semin Pediatr Neurol 1998; 5: 243-252.
    • (1998) Semin. Pediatr. Neurol. , vol.5 , pp. 243-252
    • MacCollin, M.1    Mautner, V.F.2
  • 8
    • 0034022193 scopus 로고    scopus 로고
    • Mutations and allelic loss of the NF2 gene in neurofibromatosis 2-associated skin tumors
    • Kluwe L, Friedrich RE, Hagel C, et al: Mutations and allelic loss of the NF2 gene in neurofibromatosis 2-associated skin tumors. J Invest Dermatol 2000;114:1017-1021.
    • (2000) J. Invest. Dermatol. , vol.114 , pp. 1017-1021
    • Kluwe, L.1    Friedrich, R.E.2    Hagel, C.3
  • 9
    • 0031000020 scopus 로고    scopus 로고
    • The ocular presentation of neurofibromatosis 2
    • Ragge NK, Baser ME, Riccardi VM, Falk RE: The ocular presentation of neurofibromatosis 2. Eye 1997; 11 (Pt 1): 12-18.
    • (1997) Eye , vol.11 , Issue.PART 1 , pp. 12-18
    • Ragge, N.K.1    Baser, M.E.2    Riccardi, V.M.3    Falk, R.E.4
  • 10
    • 0036358294 scopus 로고    scopus 로고
    • Presymptomatic diagnosis for children of sporadic neurofibromatosis 2 patients: A method based on tumor analysis
    • Kluwe L, Friedrich RE, Tatagiba M, Mautner VF: Presymptomatic diagnosis for children of sporadic neurofibromatosis 2 patients: A method based on tumor analysis. Genet Med 2002;4(1):27-30.
    • (2002) Genet. Med. , vol.4 , Issue.1 , pp. 27-30
    • Kluwe, L.1    Friedrich, R.E.2    Tatagiba, M.3    Mautner, V.F.4
  • 11
    • 0030968432 scopus 로고    scopus 로고
    • Management of vestibular schwannomas (acoustic neuromas): Auditory and facial nerve function after resection of 120 vestibular schwannomas in patients with neurofibromatosis 2
    • Samii M, Matthies C, Tatagiba M: Management of vestibular schwannomas (acoustic neuromas): Auditory and facial nerve function after resection of 120 vestibular schwannomas in patients with neurofibromatosis 2. Neurosurgery 1997;40: 696-705.
    • (1997) Neurosurgery , vol.40 , pp. 696-705
    • Samii, M.1    Matthies, C.2    Tatagiba, M.3
  • 12
    • 17844369150 scopus 로고    scopus 로고
    • Early proactive management of vestibular schwannomas in neurofibromatosis type 2
    • Brackmann DE, Fayad JN, Slattery WH 3rd, et al: Early proactive management of vestibular schwannomas in neurofibromatosis type 2. Neurosurgery 2001;49:274-280.
    • (2001) Neurosurgery , vol.49 , pp. 274-280
    • Brackmann, D.E.1    Fayad, J.N.2    Slattery III, W.H.3
  • 13
    • 85047677276 scopus 로고    scopus 로고
    • The parental origin of new mutations in neurofibromatosis 2
    • Kluwe L, Mautner V, Parry DM, et al: The parental origin of new mutations in neurofibromatosis 2. Neurogenetics 2000;3(1):17-24.
    • (2000) Neurogenetics , vol.3 , Issue.1 , pp. 17-24
    • Kluwe, L.1    Mautner, V.2    Parry, D.M.3
  • 14
    • 0029774092 scopus 로고    scopus 로고
    • Germ-line mutations in the neurofibromatosis 2 gene: Correlations with disease severity and retinal abnormalities
    • Parry DM, MacCollin MM, Kaiser-Kupfer MI, et al: Germ-line mutations in the neurofibromatosis 2 gene: Correlations with disease severity and retinal abnormalities. Am J Hum Genet 1996;59: 529-539.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 529-539
    • Parry, D.M.1    MacCollin, M.M.2    Kaiser-Kupfer, M.I.3
  • 15
    • 0030811426 scopus 로고    scopus 로고
    • Skin abnormalities in neurofibromatosis 2
    • Mautner VF, Lindenau M, Baser ME, et al: Skin abnormalities in neurofibromatosis 2. Arch Dermatol 1997; 133:1539-1543.
    • (1997) Arch. Dermatol. , vol.133 , pp. 1539-1543
    • Mautner, V.F.1    Lindenau, M.2    Baser, M.E.3
  • 16
    • 0036780708 scopus 로고    scopus 로고
    • Predictors of the risk of mortality in neurofibromatosis 2
    • Baser MJ, Friedman JM, Aeschliman D, et al: Predictors of the risk of mortality in neurofibromatosis 2. Am J Hum Genet 2002;71: 715-723.
    • (2002) Am. J. Hum. Genet. , vol.71 , pp. 715-723
    • Baser, M.J.1    Friedman, J.M.2    Aeschliman, D.3
  • 17
    • 19244362433 scopus 로고    scopus 로고
    • Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease
    • Ruttledge MH, Andermann AA, Phelan CM, et al: Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. Am J Hum Genet 1996;59:331-342.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 331-342
    • Ruttledge, M.H.1    Andermann, A.A.2    Phelan, C.M.3
  • 19
    • 0037323824 scopus 로고    scopus 로고
    • Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas
    • Kluwe L, Mautner V, Heinrich B, et al: Molecular study of frequency of mosaicism in neurofibromatosis 2 patients with bilateral vestibular schwannomas. J Med Genet 2003;40:109-114.
    • (2003) J. Med. Genet. , vol.40 , pp. 109-114
    • Kluwe, L.1    Mautner, V.2    Heinrich, B.3
  • 20
    • 0027302828 scopus 로고
    • Neurofibromatosis 2 in the pediatric age group
    • Mautner VF, Tatagiba M, Guthoff R, et al: Neurofibromatosis 2 in the pediatric age group. Neurosurgery 1993;33:92-96.
    • (1993) Neurosurgery , vol.33 , pp. 92-96
    • Mautner, V.F.1    Tatagiba, M.2    Guthoff, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.