메뉴 건너뛰기




Volumn 9, Issue 9, 2002, Pages 921-924

Familial idiopathic hypertrophic osteoarthropathy and atopic dermatitis (Currarino's disease);Ostéoarthropathie hypertrophique primitive familiale et dermatite atopique (maladie de currarino)

Author keywords

Child; Currarino's disease; Eczema, atopic; Hypertrophic osteoarthropathy

Indexed keywords

ARTICLE; ATOPIC DERMATITIS; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CHILD; CHRONIC DISEASE; CONSANGUINEOUS MARRIAGE; CRANIAL SUTURE; CURRARINO DISEASE; ECZEMA; FAMILIAL DISEASE; HUMAN; HYPERTROPHIC OSTEOARTHROPATHY; IDIOPATHIC DISEASE; MALE; SIBLING; SKULL DEFECT; SYNDROME;

EID: 0036740795     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(02)00024-6     Document Type: Article
Times cited : (6)

References (10)
  • 2
    • 0027452111 scopus 로고
    • Hypertrophic osteoarthropathy: Consensus on its definition, classification, assessment and diagnostic criteria
    • Martinez-Lavin M, Matucci-Cerinic M, Jajic I, Pineda C. Hypertrophic osteoarthropathy: Consensus on its definition, classification, assessment and diagnostic criteria. J Rheumatol 1993;20:1386-7.
    • (1993) J Rheumatol , vol.20 , pp. 1386-1387
    • Martinez-Lavin, M.1    Matucci-Cerinic, M.2    Jajic, I.3    Pineda, C.4
  • 3
    • 0026637411 scopus 로고
    • The spectrum of dermatological symptoms of pachydermoperiostosis (primary hypertrophic osteoarthropathy): A genetic, cytogenetic and ultrastructural study
    • Matucci-Cerinic M, Lotti T, Calvieri S, Ghersetish I, Teofoli P, Jajic I, et al. The spectrum of dermatological symptoms of pachydermoperiostosis (primary hypertrophic osteoarthropathy): a genetic, cytogenetic and ultrastructural study. Clin Exp Rheumatol 1992;10:45-8.
    • (1992) Clin Exp Rheumatol , vol.10 , pp. 45-48
    • Matucci-Cerinic, M.1    Lotti, T.2    Calvieri, S.3    Ghersetish, I.4    Teofoli, P.5    Jajic, I.6
  • 4
    • 0010528702 scopus 로고
    • Idiopathic osteoarthropathy and cranial defects in children
    • Chamberlain D, Whitaker J, Siverman F. Idiopathic osteoarthropathy and cranial defects in children. Am J Roentgenol 1965;93: 408-15.
    • (1965) Am J Roentgenol , vol.93 , pp. 408-415
    • Chamberlain, D.1    Whitaker, J.2    Siverman, F.3
  • 5
    • 0014830466 scopus 로고
    • Familial idiopathic osteoarthropathy of children: A case report and progress
    • Cremin B. Familial idiopathic osteoarthropathy of children: a case report and progress. Brit J Radiol 1970;43:568-70.
    • (1970) Brit J Radiol , vol.43 , pp. 568-570
    • Cremin, B.1
  • 8
    • 0020046473 scopus 로고
    • Familial idiopathic hypertrophic osteoarthropathy and cranial suture defects in children
    • Reginato AJ, Schiapachasse, Guerrero R. Familial idiopathic hypertrophic osteoarthropathy and cranial suture defects in children. Skeletal Radiol 1982;8:105-9.
    • (1982) Skeletal Radiol , vol.8 , pp. 105-109
    • Reginato, A.J.1    Schiapachasse2    Guerrero, R.3
  • 9
    • 0022640069 scopus 로고
    • Primary hypertrophic osteoarthropathy
    • Diren HB. Primary hypertrophic osteoarthropathy. Pediatr Radiol 1986;16:231-4.
    • (1986) Pediatr Radiol , vol.16 , pp. 231-234
    • Diren, H.B.1
  • 10
    • 0034120666 scopus 로고    scopus 로고
    • Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome
    • Chavanas S, Bodemer C, Rochat A, Hamel-Teillac D, Ali M, Irvine AD, et al. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome. Nat Genet 2000;25:141-2.
    • (2000) Nat Genet , vol.25 , pp. 141-142
    • Chavanas, S.1    Bodemer, C.2    Rochat, A.3    Hamel-Teillac, D.4    Ali, M.5    Irvine, A.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.