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Volumn 217, Issue 3, 2000, Pages 194-197

Macular dystrophy in association with Alport's syndrome;Zapfendystrophie assoziiert mit dem Alport-syndrom

Author keywords

Alport's syndrome; Cone dystrophy; Lenticonus; Macula; Renal failure; Retina; Sensorineural hearing impairment

Indexed keywords

ADULT; ALPORT SYNDROME; ARTICLE; CASE REPORT; DISEASE ASSOCIATION; HUMAN; KIDNEY FAILURE; MALE; PERCEPTION DEAFNESS; PIGMENT EPITHELIUM; RETINA MACULA DEGENERATION; RETINOPATHY; VISUAL ACUITY;

EID: 0033806910     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (23)
  • 1
    • 84965236793 scopus 로고
    • Hereditary familial congenital hemorrhagic nephritis
    • (1927) Br Med J , vol.1 , pp. 504-509
    • Alport, A.C.1
  • 6
    • 0002702691 scopus 로고
    • Alport's syndrome: Inheritance and clinical features
    • Spitzner A, Avner E, eds. Inheritance of Kidney and Renal Tract Disease. Kluwer Academic, Boston
    • (1990) , pp. 107-120
    • Flinter, F.1    Chantler, C.2
  • 9
    • 0020626685 scopus 로고
    • Ocular manifestation of Alport's syndrome: A hereditary disorder of basement membrane?
    • (1983) Br J Ophthalmol , vol.67 , pp. 493-503
    • Govan, J.A.A.1
  • 21
    • 0001067060 scopus 로고
    • Renal disease, inner ear deafness, and ocular changes: A new heredofamilial syndrome
    • (1956) Arch Int Med , vol.97 , pp. 627-630
    • Sohar, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.