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Volumn 38, Issue 5, 2009, Pages 608-609

Successful Endovascular Repair of Acute Type B Aortic Dissection in Undiagnosed Ehlers-Danlos Syndrome Type IV

Author keywords

Ehlers Danlos syndrome; Endovascular; Null alleles; Stent graft repair

Indexed keywords

COLLAGEN TYPE 3; COL3A1 PROTEIN, HUMAN;

EID: 70449707533     PISSN: 10785884     EISSN: 15322165     Source Type: Journal    
DOI: 10.1016/j.ejvs.2009.07.009     Document Type: Article
Times cited : (19)

References (5)
  • 1
    • 0034054910 scopus 로고    scopus 로고
    • Clinical and genetic features of Ehlers-Danlos syndrome type VI, the vascular type
    • Pepin M., Schwarze U., Superti-Furga A., and Byers P. Clinical and genetic features of Ehlers-Danlos syndrome type VI, the vascular type. N Engl J Med 342 (2000) 673-680
    • (2000) N Engl J Med , vol.342 , pp. 673-680
    • Pepin, M.1    Schwarze, U.2    Superti-Furga, A.3    Byers, P.4
  • 2
    • 34548073350 scopus 로고    scopus 로고
    • Endovascular abdominal aortic aneurysm repair in a patient with Ehlers-Danlos syndrome
    • Bade M.A., Queral L.A., Mukherjee D., and Kong L.S. Endovascular abdominal aortic aneurysm repair in a patient with Ehlers-Danlos syndrome. J Vasc Surg 46 (2007) 360-362
    • (2007) J Vasc Surg , vol.46 , pp. 360-362
    • Bade, M.A.1    Queral, L.A.2    Mukherjee, D.3    Kong, L.S.4
  • 3
    • 33845960990 scopus 로고    scopus 로고
    • Endovascular repair of an iliac artery aneurysm in a patient with Ehlers-Danlos syndrome type IV
    • Tonnessen B.H., Sternbergh III W., Mannava K., and Money S.R. Endovascular repair of an iliac artery aneurysm in a patient with Ehlers-Danlos syndrome type IV. J Vasc Surg 45 (2007) 177-179
    • (2007) J Vasc Surg , vol.45 , pp. 177-179
    • Tonnessen, B.H.1    Sternbergh III, W.2    Mannava, K.3    Money, S.R.4
  • 4
    • 0029902127 scopus 로고    scopus 로고
    • COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture
    • Pope F.M., Narcisi P., Nicholls A.C., Germaine D., Pals G., and Richards A.J. COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture. Br J Dermatol 135 (1996) 163-181
    • (1996) Br J Dermatol , vol.135 , pp. 163-181
    • Pope, F.M.1    Narcisi, P.2    Nicholls, A.C.3    Germaine, D.4    Pals, G.5    Richards, A.J.6
  • 5
    • 0034759627 scopus 로고    scopus 로고
    • Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV
    • Schwarze U., Schievink W.I., Petty E., Jaff M.R., Babovic-Vuksanovic D., Cherry K.J., et al. Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV. Am J Hum Genet 69 (2001) 989-1001
    • (2001) Am J Hum Genet , vol.69 , pp. 989-1001
    • Schwarze, U.1    Schievink, W.I.2    Petty, E.3    Jaff, M.R.4    Babovic-Vuksanovic, D.5    Cherry, K.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.