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Volumn 146, Issue 4, 2008, Pages 464-467

Carotid artery dissection in an adult with the Simpson-Golabi-Behmel syndrome

Author keywords

Carotid dissection; Ischemic stroke; Simpson Golabi Behmel syndrome; Vascular risk

Indexed keywords

GLYPICAN 3;

EID: 38849179499     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32154     Document Type: Article
Times cited : (15)

References (15)
  • 2
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    • A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome?
    • Behmel A, Plöch E, Rosenkranz W. 1984. A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome? Hum Genet 67:409-413.
    • (1984) Hum Genet , vol.67 , pp. 409-413
    • Behmel, A.1    Plöch, E.2    Rosenkranz, W.3
  • 4
    • 33747047598 scopus 로고    scopus 로고
    • Ischemic stroke in an adolescent with arterial tortuosity syndrome
    • Cartwright MS, Hickling WH, Roach ES. 2006. Ischemic stroke in an adolescent with arterial tortuosity syndrome. Neurology 67:360-361.
    • (2006) Neurology , vol.67 , pp. 360-361
    • Cartwright, M.S.1    Hickling, W.H.2    Roach, E.S.3
  • 6
    • 0035715062 scopus 로고    scopus 로고
    • Simpson-Golabi-Behmel syndrome: Progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition
    • DeBaun MR, Ess J, Saunders S. 2001. Simpson-Golabi-Behmel syndrome: Progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition. Mol Genet Metab 72:279-286.
    • (2001) Mol Genet Metab , vol.72 , pp. 279-286
    • DeBaun, M.R.1    Ess, J.2    Saunders, S.3
  • 7
    • 0021329881 scopus 로고
    • A new X-linked mental retardation-overgrowth syndrome
    • Golabi M, Rosen L. 1984. A new X-linked mental retardation-overgrowth syndrome. Am J Med Genet 17:345-358.
    • (1984) Am J Med Genet , vol.17 , pp. 345-358
    • Golabi, M.1    Rosen, L.2
  • 8
    • 33846163129 scopus 로고    scopus 로고
    • Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene
    • Law C, Bunyan D, Castle B, Day L, Simpson I, Westwood G, Keeton B. 2006. Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene. J Med Genet 43:908-916.
    • (2006) J Med Genet , vol.43 , pp. 908-916
    • Law, C.1    Bunyan, D.2    Castle, B.3    Day, L.4    Simpson, I.5    Westwood, G.6    Keeton, B.7
  • 11
    • 0032475859 scopus 로고    scopus 로고
    • Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome
    • Neri G, Gurrieri F, Zanni G, Lin A. 1998. Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome. Am J Med Genet 79:279-283.
    • (1998) Am J Med Genet , vol.79 , pp. 279-283
    • Neri, G.1    Gurrieri, F.2    Zanni, G.3    Lin, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.