-
1
-
-
0001927363
-
Pathologic anatomy and interrelationship of hypoplasia of the aortic tract complexes
-
Lev M. Pathologic anatomy and interrelationship of hypoplasia of the aortic tract complexes. Lab Invest 1 (1952) 61-67
-
(1952)
Lab Invest
, vol.1
, pp. 61-67
-
-
Lev, M.1
-
2
-
-
0034796502
-
Hypoplastic left-heart syndrome: the first description of the pathophysiology in 1851; translation of a publication by Dr. Bardeleben from Giessen, Germany
-
Gehrmann J., Krasemann T., Kehl H.G., and Vogt J. Hypoplastic left-heart syndrome: the first description of the pathophysiology in 1851; translation of a publication by Dr. Bardeleben from Giessen, Germany. Chest 120 (2001) 1368-1371
-
(2001)
Chest
, vol.120
, pp. 1368-1371
-
-
Gehrmann, J.1
Krasemann, T.2
Kehl, H.G.3
Vogt, J.4
-
3
-
-
35648995298
-
Contemporary results and current strategies in the management of hypoplastic left heart syndrome
-
Pigula F.A., Vida V., Del Nido P., and Bacha E. Contemporary results and current strategies in the management of hypoplastic left heart syndrome. Semin Thorac Cardiovasc Surg 19 (2007) 238-244
-
(2007)
Semin Thorac Cardiovasc Surg
, vol.19
, pp. 238-244
-
-
Pigula, F.A.1
Vida, V.2
Del Nido, P.3
Bacha, E.4
-
4
-
-
0033220507
-
The genetics of hypoplastic left heart syndrome
-
Grossfeld P.D. The genetics of hypoplastic left heart syndrome. Cardiol Young 9 (1999) 627-663
-
(1999)
Cardiol Young
, vol.9
, pp. 627-663
-
-
Grossfeld, P.D.1
-
5
-
-
0020578832
-
Morphology of ventricular septal defect associated with coarctation of aorta
-
Anderson R.H., Lenox C.C., and Zuberbuhler J.R. Morphology of ventricular septal defect associated with coarctation of aorta. Br Heart J 50 (1983) 176-181
-
(1983)
Br Heart J
, vol.50
, pp. 176-181
-
-
Anderson, R.H.1
Lenox, C.C.2
Zuberbuhler, J.R.3
-
6
-
-
36048995640
-
Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch
-
Yashiro K., Shiratori H., and Hamada H. Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch. Nature 450 (2007) 285-288
-
(2007)
Nature
, vol.450
, pp. 285-288
-
-
Yashiro, K.1
Shiratori, H.2
Hamada, H.3
-
7
-
-
33846839628
-
An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation
-
High F.A., Zhang M., Proweller A., et al. An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation. J Clin Invest 117 (2007) 353-363
-
(2007)
J Clin Invest
, vol.117
, pp. 353-363
-
-
High, F.A.1
Zhang, M.2
Proweller, A.3
-
8
-
-
0034444407
-
Epidemiology of cardiovascular malformations: prevalence and risk factors
-
Loffredo C.A. Epidemiology of cardiovascular malformations: prevalence and risk factors. Am J Med Genet 97 (2000) 319-325
-
(2000)
Am J Med Genet
, vol.97
, pp. 319-325
-
-
Loffredo, C.A.1
-
9
-
-
14044270324
-
Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions
-
Lewin M.B., McBride K.L., Pignatelli R., et al. Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions. Pediatrics 114 (2004) 691-696
-
(2004)
Pediatrics
, vol.114
, pp. 691-696
-
-
Lewin, M.B.1
McBride, K.L.2
Pignatelli, R.3
-
10
-
-
34948833712
-
Hypoplastic left heart syndrome is heritable
-
Hinton Jr. R.B., Martin L.J., Tabangin M.E., Mazwi M.L., Cripe L.H., and Benson D.W. Hypoplastic left heart syndrome is heritable. J Am Coll Cardiol 50 (2007) 1590-1595
-
(2007)
J Am Coll Cardiol
, vol.50
, pp. 1590-1595
-
-
Hinton Jr., R.B.1
Martin, L.J.2
Tabangin, M.E.3
Mazwi, M.L.4
Cripe, L.H.5
Benson, D.W.6
-
11
-
-
3242764513
-
Bicuspid aortic valve is heritable
-
Cripe L., Andelfinger G., Martin L.J., Shooner K., and Benson D.W. Bicuspid aortic valve is heritable. J Am Coll Cardiol 44 (2004) 138-143
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 138-143
-
-
Cripe, L.1
Andelfinger, G.2
Martin, L.J.3
Shooner, K.4
Benson, D.W.5
-
12
-
-
3342974500
-
The 11q terminal deletion disorder: a prospective study of 110 cases
-
Grossfeld P.D., Mattina T., Lai Z., et al. The 11q terminal deletion disorder: a prospective study of 110 cases. Am J Med Genet A 129 (2004) 51-61
-
(2004)
Am J Med Genet A
, vol.129
, pp. 51-61
-
-
Grossfeld, P.D.1
Mattina, T.2
Lai, Z.3
-
13
-
-
0035828196
-
Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE)
-
Dasgupta C., Martinez A.M., Zuppan C.W., Shah M.M., Bailey L.L., and Fletcher W.H. Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE). Mutat Res 479 (2001) 173-186
-
(2001)
Mutat Res
, vol.479
, pp. 173-186
-
-
Dasgupta, C.1
Martinez, A.M.2
Zuppan, C.W.3
Shah, M.M.4
Bailey, L.L.5
Fletcher, W.H.6
-
14
-
-
0037975739
-
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome
-
Elliott D.A., Kirk E.P., Yeoh T., et al. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. J Am Coll Cardiol 41 (2003) 2072-2076
-
(2003)
J Am Coll Cardiol
, vol.41
, pp. 2072-2076
-
-
Elliott, D.A.1
Kirk, E.P.2
Yeoh, T.3
-
15
-
-
0242636701
-
NKX2.5 mutations in patients with congenital heart disease
-
McElhinney D.B., Geiger E., Blinder J., Benson D.W., and Goldmuntz E. NKX2.5 mutations in patients with congenital heart disease. J Am Coll Cardiol 42 (2003) 1650-1655
-
(2003)
J Am Coll Cardiol
, vol.42
, pp. 1650-1655
-
-
McElhinney, D.B.1
Geiger, E.2
Blinder, J.3
Benson, D.W.4
Goldmuntz, E.5
-
16
-
-
24644467759
-
Mutations in NOTCH1 cause aortic valve disease
-
Garg V., Muth A.N., Ransom J.F., et al. Mutations in NOTCH1 cause aortic valve disease. Nature 437 (2005) 270-274
-
(2005)
Nature
, vol.437
, pp. 270-274
-
-
Garg, V.1
Muth, A.N.2
Ransom, J.F.3
-
17
-
-
43049105408
-
A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts
-
Reamon-Buettner S.M., Ciribilli Y., Inga A., and Borlak J. A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts. Hum Mol Genet 17 (2008) 1397-1405
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1397-1405
-
-
Reamon-Buettner, S.M.1
Ciribilli, Y.2
Inga, A.3
Borlak, J.4
-
18
-
-
61949160625
-
Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve
-
Hinton R.B., Martin L.J., Rame-Gowda S., Tabangin M.E., Cripe L.H., and Benson D.W. Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve. J Am Coll Cardiol 53 (2009) 1065-1071
-
(2009)
J Am Coll Cardiol
, vol.53
, pp. 1065-1071
-
-
Hinton, R.B.1
Martin, L.J.2
Rame-Gowda, S.3
Tabangin, M.E.4
Cripe, L.H.5
Benson, D.W.6
-
19
-
-
0030976787
-
Possibility of postnatal left ventricular growth in selected infants with non-apex-forming left ventricles
-
Minich L.L., Tani L.Y., Hawkins J.A., and Shaddy R.E. Possibility of postnatal left ventricular growth in selected infants with non-apex-forming left ventricles. Am Heart J 133 (1997) 570-574
-
(1997)
Am Heart J
, vol.133
, pp. 570-574
-
-
Minich, L.L.1
Tani, L.Y.2
Hawkins, J.A.3
Shaddy, R.E.4
-
20
-
-
45949092534
-
Angiotensin II blockade and aortic-root dilation in Marfan's syndrome
-
Brooke B.S., Habashi J.P., Judge D.P., Patel N., Loeys B., and Dietz III H.C. Angiotensin II blockade and aortic-root dilation in Marfan's syndrome. N Engl J Med 358 (2008) 2787-2789
-
(2008)
N Engl J Med
, vol.358
, pp. 2787-2789
-
-
Brooke, B.S.1
Habashi, J.P.2
Judge, D.P.3
Patel, N.4
Loeys, B.5
Dietz III, H.C.6
-
21
-
-
0034658189
-
World experience of percutaneous ultrasound-guided balloon valvuloplasty in human fetuses with severe aortic valve obstruction
-
Kohl T., Sharland G., Allan L.D., et al. World experience of percutaneous ultrasound-guided balloon valvuloplasty in human fetuses with severe aortic valve obstruction. Am J Cardiol 85 (2000) 1230-1233
-
(2000)
Am J Cardiol
, vol.85
, pp. 1230-1233
-
-
Kohl, T.1
Sharland, G.2
Allan, L.D.3
-
22
-
-
33645823884
-
Fetal aortic valve stenosis and the evolution of hypoplastic left heart syndrome: patient selection for fetal intervention
-
Makikallio K., McElhinney D.B., Levine J.C., et al. Fetal aortic valve stenosis and the evolution of hypoplastic left heart syndrome: patient selection for fetal intervention. Circulation 113 (2006) 1401-1405
-
(2006)
Circulation
, vol.113
, pp. 1401-1405
-
-
Makikallio, K.1
McElhinney, D.B.2
Levine, J.C.3
|