-
1
-
-
0029028630
-
Clinical and electrophysiological characteristics of atrial standstill
-
Nakazato Y, Nakata Y, Hisaoka T, Sumiyoshi M, Ogura S, Yamaguchi H. Clinical and electrophysiological characteristics of atrial standstill. Pacing Clin Electrophysiol 1995 18 : 1244 1254.
-
(1995)
Pacing Clin Electrophysiol
, vol.18
, pp. 1244-1254
-
-
Nakazato, Y.1
Nakata, Y.2
Hisaoka, T.3
Sumiyoshi, M.4
Ogura, S.5
Yamaguchi, H.6
-
2
-
-
0037420074
-
Familial dilated cardiomyopathy registry research group. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
-
Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, Carniel E, Di Lenarda A, et al. Familial dilated cardiomyopathy registry research group. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. J Am Coll Cardiol 2003 41 : 771 780.
-
(2003)
J Am Coll Cardiol
, vol.41
, pp. 771-780
-
-
Taylor, M.R.1
Fain, P.R.2
Sinagra, G.3
Robinson, M.L.4
Robertson, A.D.5
Carniel, E.6
Di Lenarda, A.7
-
3
-
-
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, Wolff MR, Porcu M, Frenneaux M, Atherton J, 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 1999 341 : 1715 1724.
-
(1999)
N Engl J Med
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
Wolff, M.R.4
Porcu, M.5
Frenneaux, M.6
Atherton, J.7
-
4
-
-
18344380431
-
Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease
-
Arbustini E, Pilotto A, Repetto A, Grasso M, Negri A, Diegoli M, Campana C, et al. Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease. J Am Coll Cardiol 2002 39 : 981 990.
-
(2002)
J Am Coll Cardiol
, vol.39
, pp. 981-990
-
-
Arbustini, E.1
Pilotto, A.2
Repetto, A.3
Grasso, M.4
Negri, A.5
Diegoli, M.6
Campana, C.7
-
5
-
-
0033927867
-
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy
-
Di Barletta MR, Ricci E, Galluzzi G, Tonali P, Mora M, Morandi L, Romorini A, et al. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. Am J Hum Genet 2000 66 : 1407 1412.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1407-1412
-
-
Di Barletta, M.R.1
Ricci, E.2
Galluzzi, G.3
Tonali, P.4
Mora, M.5
Morandi, L.6
Romorini, A.7
-
6
-
-
0037405331
-
Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype
-
Charniot JC, Pascal C, Bouchier C, Sebillon P, Salama J, Duboscq-Bidot L, Peuchmaurd M, et al. Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype. Hum Mutat 2003 21 : 473 481.
-
(2003)
Hum Mutat
, vol.21
, pp. 473-481
-
-
Charniot, J.C.1
Pascal, C.2
Bouchier, C.3
Sebillon, P.4
Salama, J.5
Duboscq-Bidot, L.6
Peuchmaurd, M.7
-
7
-
-
0033636387
-
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation
-
Becane HM, Bonne G, Varnous S, Muchir A, Ortega V, Hammouda EH, Urtizberea JA, et al. High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation. Pacing Clin Electrophysiol 2000 23 : 1661 1666.
-
(2000)
Pacing Clin Electrophysiol
, vol.23
, pp. 1661-1666
-
-
Becane, H.M.1
Bonne, G.2
Varnous, S.3
Muchir, A.4
Ortega, V.5
Hammouda, E.H.6
Urtizberea, J.A.7
-
8
-
-
0034620567
-
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
-
Brodsky GL, Muntoni F, Miocic S, Sinagra G, Sewry C, Mestroni L. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement. Circulation 2000 101 : 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
-
9
-
-
30444446953
-
Primary prevention of sudden death in patients with lamin A/C gene mutations
-
Meune C, Van Berlo JH, Anselme F, Bonne G, Pinto YM, Duboc D. Primary prevention of sudden death in patients with lamin A/C gene mutations. N Engl J Med 2006 354 : 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
-
10
-
-
0036178210
-
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse
-
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, et al. Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. Am J Hum Genet 2002 70 : 726 736.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 726-736
-
-
De Sandre-Giovannoli, A.1
Chaouch, M.2
Kozlov, S.3
Vallat, J.M.4
Tazir, M.5
Kassouri, N.6
Szepetowski, P.7
-
11
-
-
0037183491
-
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy
-
Van Der Kooi AJ, Bonne G, Eymard B, Duboc D, Talim B, Van Der Valk M, Reiss P, et al. Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy. Neurology 2002 59 : 620 623.
-
(2002)
Neurology
, vol.59
, pp. 620-623
-
-
Van Der Kooi, A.J.1
Bonne, G.2
Eymard, B.3
Duboc, D.4
Talim, B.5
Van Der Valk, M.6
Reiss, P.7
-
12
-
-
0036911038
-
A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation
-
Hershberger RE, Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Litt M. A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation. Am Heart J 2002 144 : 1081 1086.
-
(2002)
Am Heart J
, vol.144
, pp. 1081-1086
-
-
Hershberger, R.E.1
Hanson, E.L.2
Jakobs, P.M.3
Keegan, H.4
Coates, K.5
Bousman, S.6
Litt, M.7
-
13
-
-
20044374172
-
Electrophysiological and histopathological characteristics of progressive atrioventricular block accompanied by familial dilated cardiomyopathy caused by a novel mutation of lamin A/C gene
-
Otomo J, Kure S, Shiba T, Karibe A, Shinozaki T, Yagi T, Naganuma H, et al. Electrophysiological and histopathological characteristics of progressive atrioventricular block accompanied by familial dilated cardiomyopathy caused by a novel mutation of lamin A/C gene. J Cardiovasc Electrophysiol 2005 16 : 137 145.
-
(2005)
J Cardiovasc Electrophysiol
, vol.16
, pp. 137-145
-
-
Otomo, J.1
Kure, S.2
Shiba, T.3
Karibe, A.4
Shinozaki, T.5
Yagi, T.6
Naganuma, H.7
-
14
-
-
10744225746
-
Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations
-
Sanna T, Dello Russo A, Toniolo D, Vytopil M, Pelargonio G, De Martino G, Ricci E, et al. Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations. Eur Heart J 2003 24 : 2227 2236.
-
(2003)
Eur Heart J
, vol.24
, pp. 2227-2236
-
-
Sanna, T.1
Dello Russo, A.2
Toniolo, D.3
Vytopil, M.4
Pelargonio, G.5
De Martino, G.6
Ricci, E.7
-
15
-
-
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?
-
Epub: November 13, 2004.
-
van Berlo JH, de Voogt WG, Van Der Kooi AJ, van Tintelen JP, Bonne G, Yaou RB, Duboc D, 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 2005 83 : 79 83. Epub: November 13, 2004.
-
(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
Van Tintelen, J.P.4
Bonne, G.5
Yaou, R.B.6
Duboc, D.7
-
16
-
-
0037428063
-
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill
-
Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, et al. A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill. Circ Res 2003 92 : 14 22.
-
(2003)
Circ Res
, vol.92
, pp. 14-22
-
-
Groenewegen, W.A.1
Firouzi, M.2
Bezzina, C.R.3
Vliex, S.4
Van Langen, I.M.5
Sandkuijl, L.6
Smits, J.P.7
-
17
-
-
0019981849
-
Permanent atrial standstill: The clinical spectrum
-
Woolliscroft J, Tuna N. Permanent atrial standstill: The clinical spectrum. Am J Cardiol 1982 49 : 2037 2041.
-
(1982)
Am J Cardiol
, vol.49
, pp. 2037-2041
-
-
Woolliscroft, J.1
Tuna, N.2
-
18
-
-
0042164479
-
108th ENMC International workshop, 3rd workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) workshop, 13-15 September 2002, Naarden, the Netherlands
-
Bonne G, Yaou RB, Beroud C, Boriani G, Brown S, de Visser M, Duboc D, et al. 108th ENMC International workshop, 3rd workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) workshop, 13-15 September 2002, Naarden, The Netherlands. Neuromuscul Disord 2003 13 : 508 515.
-
(2003)
Neuromuscul Disord
, vol.13
, pp. 508-515
-
-
Bonne, G.1
Yaou, R.B.2
Beroud, C.3
Boriani, G.4
Brown, S.5
De Visser, M.6
Duboc, D.7
-
19
-
-
0032533246
-
Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease
-
Nelson SD, Sparks EA, Graber HL, Boudoulas H, Mehdirad AA, Baker P, Wooley C. Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease. J Am Coll Cardiol 1998 32 : 1717 1723.
-
(1998)
J Am Coll Cardiol
, vol.32
, pp. 1717-1723
-
-
Nelson, S.D.1
Sparks, E.A.2
Graber, H.L.3
Boudoulas, H.4
Mehdirad, A.A.5
Baker, P.6
Wooley, C.7
-
20
-
-
0037176263
-
Dual-chamber pacing or ventricular backup pacing in patients with an implantable defibrillator: The Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial
-
Dual Chamber and VVI Implantable Defibrillator Trial Investigators.
-
Wilkoff BL, Cook JR, Epstein AE, Greene HL, Hallstrom AP, Hsia H, Kutalek SP, et al Dual Chamber and VVI Implantable Defibrillator Trial Investigators. Dual-chamber pacing or ventricular backup pacing in patients with an implantable defibrillator: The Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial. JAMA 2002 288 : 3115 3123.
-
(2002)
JAMA
, vol.288
, pp. 3115-3123
-
-
Wilkoff, B.L.1
Cook, J.R.2
Epstein, A.E.3
Greene, H.L.4
Hallstrom, A.P.5
Hsia, H.6
Kutalek, S.P.7
Al, E.8
-
21
-
-
0036846661
-
Comparative effects of permanent biventricular and right-univentricular pacing in heart failure patients with chronic atrial fibrillation
-
Leclercq C, Walker S, Linde C, Clementy J, Marshall AJ, Ritter P, Djiane P, et al. Comparative effects of permanent biventricular and right-univentricular pacing in heart failure patients with chronic atrial fibrillation. Eur Heart J 2002 23 : 1780 1787.
-
(2002)
Eur Heart J
, vol.23
, pp. 1780-1787
-
-
Leclercq, C.1
Walker, S.2
Linde, C.3
Clementy, J.4
Marshall, A.J.5
Ritter, P.6
Djiane, P.7
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