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Volumn 23, Issue 4, 1999, Pages 347-352

Dysosteosclerosis: A case with unique dental findings and SEM evaluation of a hypoplastic tooth

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CONGENITAL MALFORMATION; DENTAL CARE; DENTAL CARIES; ENAMEL HYPOPLASIA; HUMAN; HYPODONTIA; MALE; MOLAR TOOTH; OSTEOSCLEROSIS; PATHOLOGY; TOOTH ERUPTION; TOOTH MALFORMATION;

EID: 0033149288     PISSN: 10534628     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (7)

References (17)
  • 1
    • 0003436550 scopus 로고
    • The John Hopkins University Press, Baltimore and London
    • McKusich VA. Mendelian inheritance in man. The John Hopkins University Press, Baltimore and London, 1248, 1992.
    • (1992) Mendelian Inheritance in Man , pp. 1248
    • McKusich, V.A.1
  • 8
    • 0014701996 scopus 로고
    • Manifestation der dysosteosclerosis im kieferbereich
    • Utz VW. Manifestation der dysosteosclerosis im kieferbereich. Dtsch Zahnaerztl Z 25: 48-50, 1970.
    • (1970) Dtsch Zahnaerztl Z , vol.25 , pp. 48-50
    • Utz, V.W.1
  • 9
    • 29244465814 scopus 로고
    • Paris. Flammarion Medicine Sciences
    • Lamy M eds. Maladies osseuse de 12 enfant. Paris. Flammarion Medicine Sciences, 152-53, 1974.
    • (1974) Maladies Osseuse de 12 Enfant , pp. 152-153
    • Lamy, M.1
  • 10
  • 12
    • 0025949273 scopus 로고
    • Sclerosing bone dysplasia a target site approach
    • Greespan A. Sclerosing bone dysplasia a target site approach. Skeletal Radiol 20: 561-83, 1991.
    • (1991) Skeletal Radiol , vol.20 , pp. 561-583
    • Greespan, A.1
  • 13
    • 22644440211 scopus 로고    scopus 로고
    • Case report: Dysosteosclerosis: a unique entity
    • Maheshwari A, Rao KM, Kahli N. Case report: dysosteosclerosis: a unique entity. Clinical Radiol 51: 224-28, 1996.
    • (1996) Clinical Radiol , vol.51 , pp. 224-228
    • Maheshwari, A.1    Rao, K.M.2    Kahli, N.3
  • 14
    • 0026664516 scopus 로고
    • Skeletal dysplasia, intracerebral calcifications, optic atrophy, hearing impairment and mental retardation: Nosology of dysosteosclerosis
    • Chitayat D, Silver K, Azouz EM. Skeletal dysplasia, intracerebral calcifications, optic atrophy, hearing impairment and mental retardation: nosology of dysosteosclerosis. Am J Med Gen 43: 517-23, 1992.
    • (1992) Am J Med Gen , vol.43 , pp. 517-523
    • Chitayat, D.1    Silver, K.2    Azouz, E.M.3
  • 15
    • 0023229964 scopus 로고
    • A case of autosomal recessive form of craniomethaphyseal dysplasia with unusual features and with bone fragility
    • Venturo V, Ametrano O. D'Avanzo G, Della Bruna M, Stabile M, Lonardo F. A case of autosomal recessive form of craniomethaphyseal dysplasia with unusual features and with bone fragility. Australas Radiol 31: 79-82, 1992.
    • (1992) Australas Radiol , vol.31 , pp. 79-82
    • Venturo, V.1    Ametrano, O.2    D'Avanzo, G.3    Della Bruna, M.4    Stabile, M.5    Lonardo, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.