-
1
-
-
33645116283
-
Laminopathies: multisystem dystrophy syndromes
-
Jacob K.N., and Garg A. Laminopathies: multisystem dystrophy syndromes. Mol Genet Metab 87 (2006) 289-302
-
(2006)
Mol Genet Metab
, vol.87
, pp. 289-302
-
-
Jacob, K.N.1
Garg, A.2
-
2
-
-
33748175926
-
Lamin A/C and cardiac diseases
-
Sylvius N., and Tesson F. Lamin A/C and cardiac diseases. Curr Opin Cardiol 21 (2006) 159-165
-
(2006)
Curr Opin Cardiol
, vol.21
, pp. 159-165
-
-
Sylvius, N.1
Tesson, F.2
-
3
-
-
33748296316
-
The laminopathies: a clinical review
-
Rankin J., and Ellard S. The laminopathies: a clinical review. Clin Genet 70 (2006) 261-274
-
(2006)
Clin Genet
, vol.70
, pp. 261-274
-
-
Rankin, J.1
Ellard, S.2
-
4
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
Fatkin D., MacRae C., Sasaki T., et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med 341 (1999) 1715-1724
-
(1999)
N Engl J Med
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
-
5
-
-
18344380431
-
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease
-
Arbustini E., Pilotto A., Repetto A., et al. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease. J Am Coll Cardiol 39 (2002) 981-990
-
(2002)
J Am Coll Cardiol
, vol.39
, pp. 981-990
-
-
Arbustini, E.1
Pilotto, A.2
Repetto, A.3
-
6
-
-
36148933389
-
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics
-
van Tintelen J.P., Hofstra R.M., Katerberg H., et al. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. Am Heart J 154 (2007) 1130-1139
-
(2007)
Am Heart J
, vol.154
, pp. 1130-1139
-
-
van Tintelen, J.P.1
Hofstra, R.M.2
Katerberg, H.3
-
7
-
-
10744225746
-
Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations
-
Sanna T., Dello Russo A., Toniolo D., et al. Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations. Eur Heart J 24 (2003) 2227-2236
-
(2003)
Eur Heart J
, vol.24
, pp. 2227-2236
-
-
Sanna, T.1
Dello Russo, A.2
Toniolo, D.3
-
8
-
-
0033865686
-
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
-
Bonne G., Mercuri E., Muchir A., et al. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Ann Neurol 48 (2000) 170-180
-
(2000)
Ann Neurol
, vol.48
, pp. 170-180
-
-
Bonne, G.1
Mercuri, E.2
Muchir, A.3
-
10
-
-
0034620567
-
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
-
Brodsky G.L., Muntoni F., Miocic S., Sinagra G., Sewry C., and Mestroni L. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement. Circulation 101 (2000) 473-476
-
(2000)
Circulation
, vol.101
, pp. 473-476
-
-
Brodsky, G.L.1
Muntoni, F.2
Miocic, S.3
Sinagra, G.4
Sewry, C.5
Mestroni, L.6
-
11
-
-
0037420074
-
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
-
Familial Dilated Cardiomyopathy Registry Research Group
-
Taylor M.R., Fain P.R., Sinagra G., et al., Familial Dilated Cardiomyopathy Registry Research Group. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. J Am Coll Cardiol 41 (2003) 771-780
-
(2003)
J Am Coll Cardiol
, vol.41
, pp. 771-780
-
-
Taylor, M.R.1
Fain, P.R.2
Sinagra, G.3
-
12
-
-
41949112886
-
Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function
-
Fernández X., Dumont C.A., Monserrat L., Hermida-Prieto M., and Castro-Beiras A. Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function. Int J Cardiol 12 (2007) 136-137
-
(2007)
Int J Cardiol
, vol.12
, pp. 136-137
-
-
Fernández, X.1
Dumont, C.A.2
Monserrat, L.3
Hermida-Prieto, M.4
Castro-Beiras, A.5
-
13
-
-
0034536268
-
Mutations in the LMNA gene encoding lamin A/C
-
Genschel J., and Schmidt H.H. Mutations in the LMNA gene encoding lamin A/C. Hum Mutat 16 (2000) 451-459
-
(2000)
Hum Mutat
, vol.16
, pp. 451-459
-
-
Genschel, J.1
Schmidt, H.H.2
-
14
-
-
10744225680
-
Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation
-
Forissier J.F., Bonne G., Bouchier C., et al. Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation. Eur J Heart Fail 5 (2003) 821-825
-
(2003)
Eur J Heart Fail
, vol.5
, pp. 821-825
-
-
Forissier, J.F.1
Bonne, G.2
Bouchier, C.3
-
15
-
-
34249788998
-
"Laminopathies": a wide spectrum of human diseases
-
Worman H.J., and Bonne G. "Laminopathies": a wide spectrum of human diseases. Exp Cell Res 313 (2007) 2121-2133
-
(2007)
Exp Cell Res
, vol.313
, pp. 2121-2133
-
-
Worman, H.J.1
Bonne, G.2
-
16
-
-
0033636387
-
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation
-
Bécane H.M., Bonne G., Varnous S., et al. High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation. Pacing Clin Electrophysiol 23 (2000) 1661-1666
-
(2000)
Pacing Clin Electrophysiol
, vol.23
, pp. 1661-1666
-
-
Bécane, H.M.1
Bonne, G.2
Varnous, S.3
-
17
-
-
19944431159
-
Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?
-
van Berlo J.H., de Voogt W.G., van der Kooi A.J., et al. Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?. J Mol Med 83 (2005) 79-83
-
(2005)
J Mol Med
, vol.83
, pp. 79-83
-
-
van Berlo, J.H.1
de Voogt, W.G.2
van der Kooi, A.J.3
-
18
-
-
0029864693
-
Report of the 1995 World Organization/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies
-
Richardson P., McKenna W., Bristow M., et al. Report of the 1995 World Organization/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies. Circulation 93 (1996) 841-842
-
(1996)
Circulation
, vol.93
, pp. 841-842
-
-
Richardson, P.1
McKenna, W.2
Bristow, M.3
-
19
-
-
0034944490
-
Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics
-
Gavazzi A., Repetto A., Scelsi L., et al. Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics. Eur Heart J 22 (2001) 73-81
-
(2001)
Eur Heart J
, vol.22
, pp. 73-81
-
-
Gavazzi, A.1
Repetto, A.2
Scelsi, L.3
-
20
-
-
33646384920
-
Severe dilated cardiomyopathy and quadriceps myopathy due to lamin A/C gene mutation: a phenotypic study
-
Charniot J.C., Desnos M., Zerhouni K., et al. Severe dilated cardiomyopathy and quadriceps myopathy due to lamin A/C gene mutation: a phenotypic study. Eur J Heart Fail 8 (2006) 249-256
-
(2006)
Eur J Heart Fail
, vol.8
, pp. 249-256
-
-
Charniot, J.C.1
Desnos, M.2
Zerhouni, K.3
-
21
-
-
3042519038
-
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations
-
Hermida-Prieto M., Monserrat L., Castro-Beiras A., et al. Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations. Am J Cardiol 94 (2004) 50-54
-
(2004)
Am J Cardiol
, vol.94
, pp. 50-54
-
-
Hermida-Prieto, M.1
Monserrat, L.2
Castro-Beiras, A.3
-
23
-
-
0019165493
-
Echocardiographic measurements in normal subjects from infancy to old age
-
Henry W.L., Gardin J.M., and Ware J.H. Echocardiographic measurements in normal subjects from infancy to old age. Circulation 62 (1980) 1054-1061
-
(1980)
Circulation
, vol.62
, pp. 1054-1061
-
-
Henry, W.L.1
Gardin, J.M.2
Ware, J.H.3
-
24
-
-
20944446928
-
LMNA mutation position predicts organ system involvement in laminopathies
-
Hegele R. LMNA mutation position predicts organ system involvement in laminopathies. Clin Genet 68 (2005) 31-34
-
(2005)
Clin Genet
, vol.68
, pp. 31-34
-
-
Hegele, R.1
-
25
-
-
0034120286
-
Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy
-
Arbustini E., Diegoli M., Morbini P., et al. Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy. J Am Coll Cardiol 35 (2000) 1760-1768
-
(2000)
J Am Coll Cardiol
, vol.35
, pp. 1760-1768
-
-
Arbustini, E.1
Diegoli, M.2
Morbini, P.3
-
26
-
-
34548794894
-
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
-
Benedetti S., Menditto I., Degano M., et al. Phenotypic clustering of lamin A/C mutations in neuromuscular patients. Neurology 69 (2007) 1285-1292
-
(2007)
Neurology
, vol.69
, pp. 1285-1292
-
-
Benedetti, S.1
Menditto, I.2
Degano, M.3
-
27
-
-
30444446953
-
Primary prevention of sudden death in patients with lamin A/C gene mutations
-
Meune C., Van Berlo J.H., Anselme F., Bonne G., Pinto Y.M., and Duboc D. Primary prevention of sudden death in patients with lamin A/C gene mutations. N Engl J Med 354 (2006) 209-210
-
(2006)
N Engl J Med
, vol.354
, pp. 209-210
-
-
Meune, C.1
Van Berlo, J.H.2
Anselme, F.3
Bonne, G.4
Pinto, Y.M.5
Duboc, D.6
-
28
-
-
33748609679
-
ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death-executive summary: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines
-
Zipes D.P., Camm A.J., Borggrefe M., et al. ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death-executive summary: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Develop Guidelines for Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death). J Am Coll Cardiol 48 (2006) 1064-1108
-
(2006)
J Am Coll Cardiol
, vol.48
, pp. 1064-1108
-
-
Zipes, D.P.1
Camm, A.J.2
Borggrefe, M.3
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