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Volumn 42, Issue 4, 2005, Pages 247-249

Persistent hyperplastic primary vitreous in association with neurofibromatosis 2

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASTROCYTOMA; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CATARACT; EPENDYMOMA; EYE FUNDUS; EYE INJURY; FAMILY HISTORY; GENETIC ANALYSIS; HUMAN; MALE; MENINGIOMA; NEUROFIBROMATOSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PERSISTENT HYPERPLASTIC PRIMARY VITREOUS; PHYSICAL EXAMINATION; SCHOOL CHILD; SLIT LAMP; VERTICAL TRANSMISSION; VISUAL ACUITY; VITREOUS BODY;

EID: 23044473350     PISSN: 01913913     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (10)
  • 1
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    • Goldberg MF. Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture. Am J Ophthalmol 1997;124:587-626.
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    • Goldberg, M.F.1
  • 2
    • 84907112162 scopus 로고
    • Persistent hyperplastic primary vitreous with vertical transmission
    • Lin AE, Biglan AW, Garver KL. Persistent hyperplastic primary vitreous with vertical transmission. Ophthalmic Paediatr Genet 1990;11:121-122.
    • (1990) Ophthalmic Paediatr Genet , vol.11 , pp. 121-122
    • Lin, A.E.1    Biglan, A.W.2    Garver, K.L.3
  • 3
    • 0018165133 scopus 로고
    • Persistent hyperplastic primary vitreous: A clinicopathologic study of 62 cases and review of the literature
    • Haddad R, Font RL, Reeser F. Persistent hyperplastic primary vitreous: a clinicopathologic study of 62 cases and review of the literature. Surv Ophthalmol 1978;23:123-134.
    • (1978) Surv Ophthalmol , vol.23 , pp. 123-134
    • Haddad, R.1    Font, R.L.2    Reeser, F.3
  • 4
    • 0032757197 scopus 로고    scopus 로고
    • Neurologic abnormalities associated with persistent hyperplastic primary vitreous
    • Marshman WE, Jan JE, Lyons CJ. Neurologic abnormalities associated with persistent hyperplastic primary vitreous. Can J Ophthalmol 1999;34:17-22.
    • (1999) Can J Ophthalmol , vol.34 , pp. 17-22
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  • 6
    • 0028877411 scopus 로고
    • Ocular abnormalities in neurofibromatosis 2
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    • (1995) Am J Ophthalmol , vol.120 , pp. 634-641
    • Ragge, N.K.1    Baser, M.E.2    Klein, J.3
  • 7
    • 0027405720 scopus 로고
    • A novel moesinezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumour suppressor
    • Trofatter JA, MacCollin MM, Rutter JL, et al. A novel moesinezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumour suppressor. Cell 1993;72:791-800.
    • (1993) Cell , vol.72 , pp. 791-800
    • Trofatter, J.A.1    MacCollin, M.M.2    Rutter, J.L.3
  • 8
    • 0028009140 scopus 로고
    • National Institute of Health consensus development conference statement on acoustic neuroma
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    • (1994) Arch Neurol , vol.51 , pp. 201-207
  • 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(part 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
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    • Evans, D.G.1    Huson, S.M.2    Donnai, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.