-
1
-
-
0030942788
-
What is the appropriate size criterion for resection of thoracic aortic aneurysms?
-
Coady M.A., Rizzo J.A., Hammond G.L., et al. What is the appropriate size criterion for resection of thoracic aortic aneurysms?. J Thorac Cardiovasc Surg 113 (1997) 476-491
-
(1997)
J Thorac Cardiovasc Surg
, vol.113
, pp. 476-491
-
-
Coady, M.A.1
Rizzo, J.A.2
Hammond, G.L.3
-
2
-
-
0036148137
-
Yearly rupture or dissection rates for thoracic aortic aneurysms: simple prediction based on size
-
Davies R.R., Goldstein L.J., Coady M.A., et al. Yearly rupture or dissection rates for thoracic aortic aneurysms: simple prediction based on size. Ann Thorac Surg 73 (2002) 17-28
-
(2002)
Ann Thorac Surg
, vol.73
, pp. 17-28
-
-
Davies, R.R.1
Goldstein, L.J.2
Coady, M.A.3
-
3
-
-
0023190911
-
Aortic root dilatation as a cause of isolated, severe aortic regurgitation: prevalence, clinical and echocardiographic patterns, and relation to left ventricular hypertrophy and function
-
Roman M.J., Devereux R.B., Niles N.W., et al. Aortic root dilatation as a cause of isolated, severe aortic regurgitation: prevalence, clinical and echocardiographic patterns, and relation to left ventricular hypertrophy and function. Ann Intern Med 106 (1987) 800-807
-
(1987)
Ann Intern Med
, vol.106
, pp. 800-807
-
-
Roman, M.J.1
Devereux, R.B.2
Niles, N.W.3
-
4
-
-
33748752789
-
Familial thoracic aortic aneurysms and dissections-incidence, modes of inheritance, and phenotypic patterns
-
Albornoz G., Coady M.A., Roberts M., et al. Familial thoracic aortic aneurysms and dissections-incidence, modes of inheritance, and phenotypic patterns. Ann Thorac Surg 82 (2006) 1400-1405
-
(2006)
Ann Thorac Surg
, vol.82
, pp. 1400-1405
-
-
Albornoz, G.1
Coady, M.A.2
Roberts, M.3
-
6
-
-
0035933045
-
Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14
-
Guo D., Hasham S., Kuang S.Q., et al. Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14. Circulation 103 (2001) 2461-2468
-
(2001)
Circulation
, vol.103
, pp. 2461-2468
-
-
Guo, D.1
Hasham, S.2
Kuang, S.Q.3
-
7
-
-
0020581302
-
The Marfan syndrome in early childhood: analysis of 15 patients diagnosed at less than 4 years of age
-
Sisk H.E., Zahka K.G., and Pyeritz R.E. The Marfan syndrome in early childhood: analysis of 15 patients diagnosed at less than 4 years of age. Am J Cardiol 52 (1983) 353-358
-
(1983)
Am J Cardiol
, vol.52
, pp. 353-358
-
-
Sisk, H.E.1
Zahka, K.G.2
Pyeritz, R.E.3
-
8
-
-
0026022034
-
Marfanoid children: etiologic heterogeneity and cardiac findings
-
Tayel S., Kurczynski T.W., Levine M., et al. Marfanoid children: etiologic heterogeneity and cardiac findings. Am J Dis Child 145 (1991) 90-93
-
(1991)
Am J Dis Child
, vol.145
, pp. 90-93
-
-
Tayel, S.1
Kurczynski, T.W.2
Levine, M.3
-
9
-
-
58649124954
-
Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC)
-
GenTAC Consortium
-
Eagle K.A., and GenTAC Consortium. Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC). Am Heart J 157 (2009) 319-326
-
(2009)
Am Heart J
, vol.157
, pp. 319-326
-
-
Eagle, K.A.1
-
10
-
-
0030946538
-
Familial thoracic aortic dilatations and dissections: a case control study
-
Biddinger A., Rocklin M., Coselli J., and Milewicz D.M. Familial thoracic aortic dilatations and dissections: a case control study. J Vasc Surg 25 (1997) 506-511
-
(1997)
J Vasc Surg
, vol.25
, pp. 506-511
-
-
Biddinger, A.1
Rocklin, M.2
Coselli, J.3
Milewicz, D.M.4
-
11
-
-
23744499945
-
Management of the valve and ascending aorta in adults with bicuspid aortic valve disease
-
Borger M.A., and David T.E. Management of the valve and ascending aorta in adults with bicuspid aortic valve disease. Semin Thorac Cardiovasc Surg 17 (2005) 143-147
-
(2005)
Semin Thorac Cardiovasc Surg
, vol.17
, pp. 143-147
-
-
Borger, M.A.1
David, T.E.2
-
12
-
-
37249002743
-
Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature
-
Carlson M., and Silberbach M. Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature. J Med Genet 44 (2007) 745-749
-
(2007)
J Med Genet
, vol.44
, pp. 745-749
-
-
Carlson, M.1
Silberbach, M.2
-
13
-
-
0033017099
-
Familial patterns of thoracic aortic aneurysms
-
Coady M.A., Davies R.R., Roberts M., et al. Familial patterns of thoracic aortic aneurysms. Arch Surg 134 (1999) 361-367
-
(1999)
Arch Surg
, vol.134
, pp. 361-367
-
-
Coady, M.A.1
Davies, R.R.2
Roberts, M.3
-
14
-
-
4344571746
-
Perspectives on diseases of the thoracic aorta
-
Elefteriades J.A. Perspectives on diseases of the thoracic aorta. Adv Cardiol 41 (2004) 75-86
-
(2004)
Adv Cardiol
, vol.41
, pp. 75-86
-
-
Elefteriades, J.A.1
-
15
-
-
0031816340
-
Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications
-
Groenink M., Rozendaal L., Naeff M.S., et al. Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications. Heart 80 (1998) 163-169
-
(1998)
Heart
, vol.80
, pp. 163-169
-
-
Groenink, M.1
Rozendaal, L.2
Naeff, M.S.3
-
16
-
-
36549071997
-
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections
-
[Erratum: Nat Genet 2008;40:255]
-
Guo D.-C., Pannu H., Tran-Fadulu V., et al. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. [Erratum: Nat Genet 2008;40:255]. Nat Genet 39 (2007) 1488-1493
-
(2007)
Nat Genet
, vol.39
, pp. 1488-1493
-
-
Guo, D.-C.1
Pannu, H.2
Tran-Fadulu, V.3
-
17
-
-
0034243015
-
Ruptured aortic dissecting aneurysm in Turner's syndrome: a case report and review of literature
-
Hirose H., Amano A., Takahashi A., Nagano N., and Kohmoto T. Ruptured aortic dissecting aneurysm in Turner's syndrome: a case report and review of literature. Ann Thorac Cardiovasc Surg 6 (2000) 275-280
-
(2000)
Ann Thorac Cardiovasc Surg
, vol.6
, pp. 275-280
-
-
Hirose, H.1
Amano, A.2
Takahashi, A.3
Nagano, N.4
Kohmoto, T.5
-
18
-
-
33947595399
-
Progressive dilation of the ascending aorta in children with isolated bicuspid aortic valve
-
Holmes K.W., Lehmann C.U., Dalal D., et al. Progressive dilation of the ascending aorta in children with isolated bicuspid aortic valve. Am J Cardiol 99 (2007) 978-983
-
(2007)
Am J Cardiol
, vol.99
, pp. 978-983
-
-
Holmes, K.W.1
Lehmann, C.U.2
Dalal, D.3
-
19
-
-
0027213775
-
The natural history of aortic dilatation in Marfan syndrome
-
Hwa J., Richards J.G., Huang H., et al. The natural history of aortic dilatation in Marfan syndrome. Med J Aust 158 (1993) 558-562
-
(1993)
Med J Aust
, vol.158
, pp. 558-562
-
-
Hwa, J.1
Richards, J.G.2
Huang, H.3
-
20
-
-
0032111101
-
Further delineation of aortic dilation, dissection, and rupture in patients with Turner syndrome
-
Lin A.E., Lippe B., and Rosenfeld R.G. Further delineation of aortic dilation, dissection, and rupture in patients with Turner syndrome. Pediatrics 102 (1998) e12
-
(1998)
Pediatrics
, vol.102
-
-
Lin, A.E.1
Lippe, B.2
Rosenfeld, R.G.3
-
21
-
-
20144367207
-
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., 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
-
22
-
-
33747812887
-
Aneurysm syndromes caused by mutations in the TGF-β receptor
-
Loeys B.L., Schwarze U., Holm T., et al. Aneurysm syndromes caused by mutations in the TGF-β receptor. N Engl J Med 355 (2006) 788-798
-
(2006)
N Engl J Med
, vol.355
, pp. 788-798
-
-
Loeys, B.L.1
Schwarze, U.2
Holm, T.3
-
23
-
-
0034054910
-
Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type
-
[Erratum: N Engl J Med 2001;344:392]
-
Pepin M., Schwarze U., Superti-Furga A., and Byers P.H. Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type. [Erratum: N Engl J Med 2001;344:392]. 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.H.4
-
25
-
-
33644627494
-
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus
-
Zhu L., Vranckx R., Khau Van Kien P., et al. Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus. Nat Genet 38 (2006) 343-349
-
(2006)
Nat Genet
, vol.38
, pp. 343-349
-
-
Zhu, L.1
Vranckx, R.2
Khau Van Kien, P.3
-
26
-
-
0036840603
-
Natural history of thoracic aortic aneurysms: indications for surgery, and surgical versus nonsurgical risks
-
Elefteriades J.A. Natural history of thoracic aortic aneurysms: indications for surgery, and surgical versus nonsurgical risks. Ann Thorac Surg 74 (2002) S1877-S1880
-
(2002)
Ann Thorac Surg
, vol.74
-
-
Elefteriades, J.A.1
-
27
-
-
43649086088
-
Aortic root operations for Marfan syndrome: a comparison of the Bentall and valve-sparing procedures
-
Patel N.D., Weiss E.S., Alejo D.E., et al. Aortic root operations for Marfan syndrome: a comparison of the Bentall and valve-sparing procedures. Ann Thorac Surg 85 (2008) 2003-2011
-
(2008)
Ann Thorac Surg
, vol.85
, pp. 2003-2011
-
-
Patel, N.D.1
Weiss, E.S.2
Alejo, D.E.3
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