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Volumn 33, Issue 2, 2001, Pages 131-135

Spontaneous capsular ruptures in Alport syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALPORT SYNDROME; ARTICLE; CHRONIC KIDNEY FAILURE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; FAMILY HISTORY; FEMALE; FOLLOW UP; HEMATURIA; HUMAN; LENS CAPSULE; LENS DISEASE; LENS IMPLANTATION; MALE; PERCEPTION DEAFNESS; PRESCHOOL CHILD; TREATMENT OUTCOME; VISUAL ACUITY;

EID: 0034931206     PISSN: 15304086     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12009-001-0008-y     Document Type: Article
Times cited : (10)

References (35)
  • 1
    • 84965236793 scopus 로고
    • Hereditary familial congenital hemorrhagic nephritis
    • (1927) Br Med J , vol.1 , pp. 504-506
    • Alport, A.C.1
  • 2
    • 0001067060 scopus 로고
    • Renal disease, inner ear deafness and ocular changes: A new heredofamilial syndrome
    • (1956) Arch Intern Med , vol.97 , pp. 627-630
    • Sohar, E.1
  • 6
    • 0020626685 scopus 로고
    • Ocular manifestations of Alport's syndrome: A hereditary disorder of basement membranes?
    • (1983) Br J Ophthalmol , vol.67 , pp. 493-503
    • Govan, J.A.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.