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Volumn 133, Issue 1, 2007, Pages

Valve-sparing aortic root replacement in a patient with a rare connective tissue disorder: Arterial tortuosity syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ANTITHROMBOCYTIC AGENT;

EID: 33845763446     PISSN: 00225223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jtcvs.2006.08.050     Document Type: Article
Times cited : (14)

References (5)
  • 1
    • 0031005857 scopus 로고    scopus 로고
    • Surgery of the thoracic aorta
    • Kouchoukos N.T., and Dougenis D. Surgery of the thoracic aorta. N Engl J Med 336 (1997) 1876-1888
    • (1997) N Engl J Med , vol.336 , pp. 1876-1888
    • Kouchoukos, N.T.1    Dougenis, D.2
  • 2
    • 0028842262 scopus 로고
    • Repair of the aortic valve in patients with aortic insufficiency and aortic root aneurysm
    • David T.E., Feindel C.M., and Bos J. Repair of the aortic valve in patients with aortic insufficiency and aortic root aneurysm. J Thorac Cardiovasc Surg 109 (1995) 345-352
    • (1995) J Thorac Cardiovasc Surg , vol.109 , pp. 345-352
    • David, T.E.1    Feindel, C.M.2    Bos, J.3
  • 3
    • 0345103458 scopus 로고    scopus 로고
    • Early and long-term results of a valve-sparing operation for Marfan syndrome
    • Birks E.J., Webb C., Child A., Radley-Smith R., and Yacoub M.H. Early and long-term results of a valve-sparing operation for Marfan syndrome. Circulation 100 suppl (1999) II29-II35
    • (1999) Circulation , vol.100 , Issue.SUPPL
    • Birks, E.J.1    Webb, C.2    Child, A.3    Radley-Smith, R.4    Yacoub, M.H.5
  • 4
    • 33645381280 scopus 로고    scopus 로고
    • Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
    • Coucke P.J., Willaert A., Wessels M.W., Callewaert B., Zoppi N., De Backer J., et al. Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome. Nat Genet 38 (2006) 452-457
    • (2006) Nat Genet , vol.38 , pp. 452-457
    • Coucke, P.J.1    Willaert, A.2    Wessels, M.W.3    Callewaert, B.4    Zoppi, N.5    De Backer, J.6
  • 5
    • 20144367207 scopus 로고    scopus 로고
    • A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
    • Loeys B.L., Chen J., Neptune E.R., Judge D.P., Podowski M., Holm T., et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet 37 (2005) 275-281
    • (2005) Nat Genet , vol.37 , pp. 275-281
    • Loeys, B.L.1    Chen, J.2    Neptune, E.R.3    Judge, D.P.4    Podowski, M.5    Holm, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.