메뉴 건너뛰기




Volumn 216, Issue 3, 2008, Pages 236-238

Nevus marginatus: A distinct type of epidermal nevus or merely a variant of nevus sebaceus?

Author keywords

Congenital; Epidermal nevus; Sebaceous gland

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 3;

EID: 40949121089     PISSN: 10188665     EISSN: None     Source Type: Journal    
DOI: 10.1159/000112933     Document Type: Article
Times cited : (7)

References (17)
  • 2
    • 58149211750 scopus 로고
    • Epidermal nevus syndromes
    • Happle R: Epidermal nevus syndromes. Semin Dermatol 1995;14:111-121.
    • (1995) Semin Dermatol , vol.14 , pp. 111-121
    • Happle, R.1
  • 3
    • 0032971417 scopus 로고    scopus 로고
    • The spectrum of epidermal nevi: A case of verrucous epidermal nevus contiguous with nevus sebaceus
    • Waltz KM, Helm KF, Billingsley EM: The spectrum of epidermal nevi: a case of verrucous epidermal nevus contiguous with nevus sebaceus. Pediatr Dermatol 1999;16:211-213.
    • (1999) Pediatr Dermatol , vol.16 , pp. 211-213
    • Waltz, K.M.1    Helm, K.F.2    Billingsley, E.M.3
  • 4
    • 0029069311 scopus 로고
    • What is a nevus? A proposed definition of a common medical term
    • Happle R: What is a nevus? A proposed definition of a common medical term. Dermatology 1995;191:1-5.
    • (1995) Dermatology , vol.191 , pp. 1-5
    • Happle, R.1
  • 5
    • 0027452134 scopus 로고
    • Mosaicism in human skin: Understanding the patterns and mechanisms
    • Happle R: Mosaicism in human skin: understanding the patterns and mechanisms. Arch Dermatol 1993;129:1460-1470.
    • (1993) Arch Dermatol , vol.129 , pp. 1460-1470
    • Happle, R.1
  • 6
    • 27744600116 scopus 로고    scopus 로고
    • A simple and fast method for the simultaneous detection of nine fibroblast growth factor receptor 3 mutations in bladder cancer and voided urine
    • van Oers JM, Lurkin I, van Exsel AJ, et al: A simple and fast method for the simultaneous detection of nine fibroblast growth factor receptor 3 mutations in bladder cancer and voided urine. Clin Cancer Res 2005;11:7743-7748.
    • (2005) Clin Cancer Res , vol.11 , pp. 7743-7748
    • van Oers, J.M.1    Lurkin, I.2    van Exsel, A.J.3
  • 7
    • 33746754183 scopus 로고    scopus 로고
    • Mosaicism of activating FGFR3 mutations in human skin causes epidermal nevi
    • Hafner C, van Oers JM, Vogt T, et al: Mosaicism of activating FGFR3 mutations in human skin causes epidermal nevi. J Clin Invest 2006;116:2201-2207.
    • (2006) J Clin Invest , vol.116 , pp. 2201-2207
    • Hafner, C.1    van Oers, J.M.2    Vogt, T.3
  • 9
    • 0016577757 scopus 로고
    • Epidermal and other congenital organoid nevi
    • Solomon LM, Esterly NB: Epidermal and other congenital organoid nevi. Curr Probl Pediatr 1975;6:1-56.
    • (1975) Curr Probl Pediatr , vol.6 , pp. 1-56
    • Solomon, L.M.1    Esterly, N.B.2
  • 12
    • 0025808092 scopus 로고
    • How many epidermal nevus syndromes exist? A clinicogenetic classification
    • Happle R: How many epidermal nevus syndromes exist? A clinicogenetic classification. J Am Acad Dermatol 1991;25:550-556.
    • (1991) J Am Acad Dermatol , vol.25 , pp. 550-556
    • Happle, R.1
  • 13
    • 0026781694 scopus 로고
    • Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis
    • Rothnagel JA, Dominey AM, Dempsey LD, et al: Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis. Science 1992;257:1128-1130.
    • (1992) Science , vol.257 , pp. 1128-1130
    • Rothnagel, J.A.1    Dominey, A.M.2    Dempsey, L.D.3
  • 14
    • 0028135470 scopus 로고
    • Genetic and clinical mosaicism in a type of epidermal nevus
    • Paller AS, Syder AJ, Chan YM, et al: Genetic and clinical mosaicism in a type of epidermal nevus. N Engl J Med 1994;331:1408-1415.
    • (1994) N Engl J Med , vol.331 , pp. 1408-1415
    • Paller, A.S.1    Syder, A.J.2    Chan, Y.M.3
  • 15
    • 0033972847 scopus 로고    scopus 로고
    • Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome
    • Konig A, Happle R, Bornholdt D, Engel H, Grzeschik KH: Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am J Med Genet 2000;90:339-346.
    • (2000) Am J Med Genet , vol.90 , pp. 339-346
    • Konig, A.1    Happle, R.2    Bornholdt, D.3    Engel, H.4    Grzeschik, K.H.5
  • 16
    • 0033561652 scopus 로고    scopus 로고
    • The sebaceous nevus: A nevus with deletions of the PTCH gene
    • Xin H, Matt D, Qin JZ, Burg G, Boni R: The sebaceous nevus: a nevus with deletions of the PTCH gene. Cancer Res 1999;59:1834-1836.
    • (1999) Cancer Res , vol.59 , pp. 1834-1836
    • Xin, H.1    Matt, D.2    Qin, J.Z.3    Burg, G.4    Boni, R.5
  • 17
    • 0035671651 scopus 로고    scopus 로고
    • No evidence of deregulated patched-hedgehog signaling pathway in trichoblastomas and other tumors arising within nevus sebaceus
    • Takata M, Tojo M, Hatta N, Ohara K, Yamada M, Takehara K: No evidence of deregulated patched-hedgehog signaling pathway in trichoblastomas and other tumors arising within nevus sebaceus. J Invest Dermatol 2001;117:1666-1670.
    • (2001) J Invest Dermatol , vol.117 , pp. 1666-1670
    • Takata, M.1    Tojo, M.2    Hatta, N.3    Ohara, K.4    Yamada, M.5    Takehara, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.