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Volumn 66, Issue 4, 2012, Pages 617-621

Folliculocystic and collagen hamartoma of tuberous sclerosis complex

Author keywords

collagen nevus; hamartoma; tuberous sclerosis complex

Indexed keywords

COLLAGEN; KERATIN;

EID: 84858333891     PISSN: 01909622     EISSN: 10976787     Source Type: Journal    
DOI: 10.1016/j.jaad.2011.04.002     Document Type: Article
Times cited : (38)

References (12)
  • 1
    • 0032438210 scopus 로고    scopus 로고
    • Tuberous sclerosis complex consensus conference: Revised clinical diagnostic criteria
    • E.S. Roach, M.R. Gomez, and H. Northrup Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria J Child Neurol 13 1998 624 628
    • (1998) J Child Neurol , vol.13 , pp. 624-628
    • Roach, E.S.1    Gomez, M.R.2    Northrup, H.3
  • 3
    • 0032424306 scopus 로고    scopus 로고
    • Skin lesions in children with tuberous sclerosis complex: Their prevalence, natural course, and diagnostic significance
    • S. Jóźwiak, R.A. Schwartz, C.K. Janniger, R. Michałowicz, and J. Chmielik Skin lesions in children with tuberous sclerosis complex: their prevalence, natural course, and diagnostic significance Int J Dermatol 37 1998 911 917
    • (1998) Int J Dermatol , vol.37 , pp. 911-917
    • Jóźwiak, S.1    Schwartz, R.A.2    Janniger, C.K.3    Michałowicz, R.4    Chmielik, J.5
  • 4
    • 13544274478 scopus 로고    scopus 로고
    • Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis
    • J. Hellemans, O. Preobrazhenska, A. Willaert, P. Debeer, P.C. Verdonk, and T. Costa Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis Nat Genet 36 2004 1213 1218
    • (2004) Nat Genet , vol.36 , pp. 1213-1218
    • Hellemans, J.1    Preobrazhenska, O.2    Willaert, A.3    Debeer, P.4    Verdonk, P.C.5    Costa, T.6
  • 6
  • 7
    • 0346447959 scopus 로고
    • Symmetric nevi of the face, tuberous sclerosis, epilepsy and fibromatous growth on scalp: With abnormal electroencephalograms of members of the family; Report of a case
    • C.K. Good, and J. Garb Symmetric nevi of the face, tuberous sclerosis, epilepsy and fibromatous growth on scalp: with abnormal electroencephalograms of members of the family; report of a case Arch Dermatol Syph 47 1943 197 215
    • (1943) Arch Dermatol Syph , vol.47 , pp. 197-215
    • Good, C.K.1    Garb, J.2
  • 8
    • 0003180519 scopus 로고
    • Tuberous sclerosis: Special reference to the microscopic alterations in the cutaneous hamartomas
    • W.R. Nickel, and W.B. Reed Tuberous sclerosis: special reference to the microscopic alterations in the cutaneous hamartomas Arch Dermatol 85 1962 209 226
    • (1962) Arch Dermatol , vol.85 , pp. 209-226
    • Nickel, W.R.1    Reed, W.B.2
  • 9
    • 68549109637 scopus 로고    scopus 로고
    • Fibrofolliculoma/trichodiscoma and fibrous papule (perifollicular fibroma/angiofibroma): A revaluation of the histopathological and immunohistochemical features
    • N. Misago, T. Kimura, and Y. Narisawa Fibrofolliculoma/trichodiscoma and fibrous papule (perifollicular fibroma/angiofibroma): a revaluation of the histopathological and immunohistochemical features J Cutan Pathol 36 2009 943 951
    • (2009) J Cutan Pathol , vol.36 , pp. 943-951
    • Misago, N.1    Kimura, T.2    Narisawa, Y.3
  • 10
    • 0017571247 scopus 로고
    • Multiplefibrofolliculomas (Birt-Hogg-Dubé) associated with a large connective tissue nevus
    • R. Weintraub, and H. Pinkus Multiplefibrofolliculomas (Birt-Hogg-Dubé) associated with a large connective tissue nevus J Cutan Pathol 4 1977 289 299
    • (1977) J Cutan Pathol , vol.4 , pp. 289-299
    • Weintraub, R.1    Pinkus, H.2
  • 11
    • 69149110763 scopus 로고    scopus 로고
    • A large infiltrating fibrous hamartoma of infancy in the abdominal wall with rare associated tuberous sclerosis
    • H.-J. Han, G.Y. Lim, and C.Y. You A large infiltrating fibrous hamartoma of infancy in the abdominal wall with rare associated tuberous sclerosis Pediatr Radiol 39 2009 743 746
    • (2009) Pediatr Radiol , vol.39 , pp. 743-746
    • Han, H.-J.1    Lim, G.Y.2    You, C.Y.3
  • 12
    • 0035023941 scopus 로고    scopus 로고
    • Segmental type 2 manifestation of autosome dominant skin diseases: Development of a new formal genetic concept
    • R. Happle Segmental type 2 manifestation of autosome dominant skin diseases: development of a new formal genetic concept Hautarzt 52 2001 283 287
    • (2001) Hautarzt , vol.52 , pp. 283-287
    • Happle, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.