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Volumn 53, Issue 3, 1999, Pages 629-631

Cerebroretinal vasculopathy mimicking a brain tumor: A case of a rare hereditary syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN TUMOR; CASE REPORT; CEREBRORETINAL VASCULOPATHY; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; FAMILY HISTORY; FRONTAL CORTEX; HUMAN; HUMAN TISSUE; MALE; MICROCIRCULATION; PRIORITY JOURNAL; RETINA BLOOD FLOW; RETINA BLOOD VESSEL; VASCULAR DISEASE;

EID: 0033546629     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.53.3.629     Document Type: Article
Times cited : (45)

References (9)
  • 1
    • 0023923348 scopus 로고
    • Cerebroretinal vasculopathy. A new hereditary syndrome
    • Grand MG, Kaine J, Fulling K, et al. Cerebroretinal vasculopathy. A new hereditary syndrome. Ophthalmology 1988;95:649-659.
    • (1988) Ophthalmology , vol.95 , pp. 649-659
    • Grand, M.G.1    Kaine, J.2    Fulling, K.3
  • 2
    • 0024465713 scopus 로고
    • Hereditary retinal vasculopathy with cerebral white matter lesions
    • Gutmann DH, Fischbeck KH, Sergott RC. Hereditary retinal vasculopathy with cerebral white matter lesions. Am J Med Genet 1989;34:217-220.
    • (1989) Am J Med Genet , vol.34 , pp. 217-220
    • Gutmann, D.H.1    Fischbeck, K.H.2    Sergott, R.C.3
  • 3
    • 0030712287 scopus 로고    scopus 로고
    • Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)
    • Jen J, Cohen AH, Yue Q, et al. Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS). Neurology 1997;49:1322-1330.
    • (1997) Neurology , vol.49 , pp. 1322-1330
    • Jen, J.1    Cohen, A.H.2    Yue, Q.3
  • 6
    • 0344533817 scopus 로고
    • Retinal telangiectasia
    • Yannuzzi LA, Gitter KA, Schatz H, eds. Baltimore: Williams & Wilkins
    • Gitter KA, Yannuzzi LA, Schatz H. Retinal telangiectasia. In: Yannuzzi LA, Gitter KA, Schatz H, eds. The macula: comprehensive text and atlas. Baltimore: Williams & Wilkins, 1979: 118-126.
    • (1979) The Macula: Comprehensive Text and Atlas , pp. 118-126
    • Gitter, K.A.1    Yannuzzi, L.A.2    Schatz, H.3
  • 7
    • 0022414098 scopus 로고
    • Retinal telangiectasis in facioscapulohumeral muscular dystrophy with deafness
    • Gurwin EB, Fitzsimons RB, Sehmi KS, Bird AC. Retinal telangiectasis in facioscapulohumeral muscular dystrophy with deafness. Arch Ophthalmol 1985;103:1695-1700.
    • (1985) Arch Ophthalmol , vol.103 , pp. 1695-1700
    • Gurwin, E.B.1    Fitzsimons, R.B.2    Sehmi, K.S.3    Bird, A.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.