-
1
-
-
0028116218
-
Idiopathic dilated cardiomyopathy
-
Dec GW, Fuster V. Idiopathic dilated cardiomyopathy. N Engl J Med 1994;23:1564-75.
-
(1994)
N Engl J Med
, vol.23
, pp. 1564-1575
-
-
Dec, G.W.1
Fuster, V.2
-
2
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
Michels VV, Moll PP, Miller FA, Tajik AJ, Chu JS, Driscoll DJ, Burnett JC, Rodeheffer RJ, Chesebro JH, Tazelaar HD. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Engl J Med 1992;326:77-82.
-
(1992)
N Engl J Med
, vol.326
, pp. 77-82
-
-
Michels, V.V.1
Moll, P.P.2
Miller, F.A.3
Tajik, A.J.4
Chu, J.S.5
Driscoll, D.J.6
Burnett, J.C.7
Rodeheffer, R.J.8
Chesebro, J.H.9
Tazelaar, H.D.10
-
3
-
-
0029009393
-
Familial dilated cardiomyopathy in the United Kingdom
-
Keeling PJ, Gang Y, Smith G, Seo H, Bent SE, Murday V, Caforio ALP, McKenna WJ. Familial dilated cardiomyopathy in the United Kingdom. Br Heart J 1995;73:417-21.
-
(1995)
Br Heart J
, vol.73
, pp. 417-421
-
-
Keeling, P.J.1
Gang, Y.2
Smith, G.3
Seo, H.4
Bent, S.E.5
Murday, V.6
Caforio, A.L.P.7
McKenna, W.J.8
-
4
-
-
0031951537
-
Frequency and phenotypes of familial dilated cardiomyopathy
-
Grünig E, Tasman JA, Kücherer H, Franz W, Kübler W, Katus HA. Frequency and phenotypes of familial dilated cardiomyopathy. J Am Coll Cardiol 1998;31:186-94.
-
(1998)
J Am Coll Cardiol
, vol.31
, pp. 186-194
-
-
Grünig, E.1
Tasman, J.A.2
Kücherer, H.3
Franz, W.4
Kübler, W.5
Katus, H.A.6
-
5
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 1998;280:750-2.
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
6
-
-
0033520037
-
Desmin mutation responsible for idiopathic dilated cardiomyopathy
-
Li D, Tapscoft T, Gonzalez O, Butch PE, Quinones MA, Zoghbi WA, Hill R, Bachinski LL, Mann DL, Roberts R. Desmin mutation responsible for idiopathic dilated cardiomyopathy. Circulation 1999;100:461-4.
-
(1999)
Circulation
, vol.100
, pp. 461-464
-
-
Li, D.1
Tapscoft, T.2
Gonzalez, O.3
Butch, P.E.4
Quinones, M.A.5
Zoghbi, W.A.6
Hill, R.7
Bachinski, L.L.8
Mann, D.L.9
Roberts, R.10
-
7
-
-
0033818186
-
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
-
Tsubata S, Bowles KR, Vatta M, Zintz C, Titus J, Muhonen L, Bowles NE, Towbin JA. Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. J Clin Invest 2000;106:655-62.
-
(2000)
J Clin Invest
, vol.106
, pp. 655-662
-
-
Tsubata, S.1
Bowles, K.R.2
Vatta, M.3
Zintz, C.4
Titus, J.5
Muhonen, L.6
Bowles, N.E.7
Towbin, J.A.8
-
8
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharma P, McDonough B, Smoot L, Mullen MP, Woolf PK, Wigle ED, Seidman JG, Seidman CE, Kimura M, Furutani Y, Furutani M, Takao A, Momma K, Matsuoka R, Yamagishi H, Morikawa Y, Kojima Y, Hino Y, Imamura S. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N Engl J Med 2000;343:1688-96.
-
(2000)
N Engl J Med
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
McDonough, B.6
Smoot, L.7
Mullen, M.P.8
Woolf, P.K.9
Wigle, E.D.10
Seidman, J.G.11
Seidman, C.E.12
Kimura, M.13
Furutani, Y.14
Furutani, M.15
Takao, A.16
Momma, K.17
Matsuoka, R.18
Yamagishi, H.19
Morikawa, Y.20
Kojima, Y.21
Hino, Y.22
Imamura, S.23
more..
-
9
-
-
0035975958
-
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
-
Li D, Czernuszewicz GZ, Gonzalez O, Tapscott T, Karibe A, Durand JB, Brugada R, Hill R, Gregoritch JM, Anderson JL, Quinones M, Bachinski LL, Roberts R. Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy. Circulation 2001;104:2188-93.
-
(2001)
Circulation
, vol.104
, pp. 2188-2193
-
-
Li, D.1
Czernuszewicz, G.Z.2
Gonzalez, O.3
Tapscott, T.4
Karibe, A.5
Durand, J.B.6
Brugada, R.7
Hill, R.8
Gregoritch, J.M.9
Anderson, J.L.10
Quinones, M.11
Bachinski, L.L.12
Roberts, R.13
-
10
-
-
0036401384
-
Novel mutations in sarcomeric protein genes in dilated cardiomyopathy
-
Daehmlow S, Erdmann J, Knueppel T, Gille C, Froemmel C, Hummel M, Hetzer R, Regitz-Zagrosek V. Novel mutations in sarcomeric protein genes in dilated cardiomyopathy. Biochem Biophys Res Commun 2002;298:116-20.
-
(2002)
Biochem Biophys Res Commun
, vol.298
, pp. 116-120
-
-
Daehmlow, S.1
Erdmann, J.2
Knueppel, T.3
Gille, C.4
Froemmel, C.5
Hummel, M.6
Hetzer, R.7
Regitz-Zagrosek, V.8
-
11
-
-
0034971165
-
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
-
Olson TM, Kishimoto NY, Whitby FG, Michels VV. Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy. J Mol Cell Cardiol 2001;33:723-32.
-
(2001)
J Mol Cell Cardiol
, vol.33
, pp. 723-732
-
-
Olson, T.M.1
Kishimoto, N.Y.2
Whitby, F.G.3
Michels, V.V.4
-
12
-
-
0036478897
-
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
-
Gerull B, Gramlich M, Atherton J, McNabb M, Trombitas K, Sasse-Klaassen S, Seidman JG, Seidman C, Granzier H, Labeit S, Frenneaux M, Thierfelder L. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy. Nat Genet 2002;30:201-4.
-
(2002)
Nat Genet
, vol.30
, pp. 201-204
-
-
Gerull, B.1
Gramlich, M.2
Atherton, J.3
McNabb, M.4
Trombitas, K.5
Sasse-Klaassen, S.6
Seidman, J.G.7
Seidman, C.8
Granzier, H.9
Labeit, S.10
Frenneaux, M.11
Thierfelder, L.12
-
13
-
-
0037192309
-
Metavinculin mutations alter actin interaction in dilated cardiomyopathy
-
Olson TM, Illenberger S, Kishimoto NY, Huttelmaier S, Keating MT, Jockusch BM. Metavinculin mutations alter actin interaction in dilated cardiomyopathy. Circulation 2002;105:431-7.
-
(2002)
Circulation
, vol.105
, pp. 431-437
-
-
Olson, T.M.1
Illenberger, S.2
Kishimoto, N.Y.3
Huttelmaier, S.4
Keating, M.T.5
Jockusch, B.M.6
-
14
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
Knoll, R, Hoshijima M, Hoffman HM, Person V, Lorenzen-Schmidt I, Bang ML, Hayashi T, Shiga N, Yasukawa H, Schaper W, McKenna W, Yokoyama M, Schork NJ, Omens JH, McCulloch AD, Kimura A, Gregorio CC, Poller W, Schaper J, Schultheiss HP, Chien KR. The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell 2002;111:943-55.
-
(2002)
Cell
, vol.111
, pp. 943-955
-
-
Knoll, R.1
Hoshijima, M.2
Hoffman, H.M.3
Person, V.4
Lorenzen-Schmidt, I.5
Bang, M.L.6
Hayashi, T.7
Shiga, N.8
Yasukawa, H.9
Schaper, W.10
McKenna, W.11
Yokoyama, M.12
Schork, N.J.13
Omens, J.H.14
McCulloch, A.D.15
Kimura, A.16
Gregorio, C.C.17
Poller, W.18
Schaper, J.19
Schultheiss, H.P.20
Chien, K.R.21
more..
-
15
-
-
0037470512
-
Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban
-
Schmitt, JP, Kamisago M, Asahi M, Li GH, Ahmad F, Mende U, Kranias EG, MacLennan DH, Seidman JG, Seidman CE. Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban. Science 2003;299:1410-13.
-
(2003)
Science
, vol.299
, pp. 1410-1413
-
-
Schmitt, J.P.1
Kamisago, M.2
Asahi, M.3
Li, G.H.4
Ahmad, F.5
Mende, U.6
Kranias, E.G.7
MacLennan, D.H.8
Seidman, J.G.9
Seidman, C.E.10
-
16
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne G, Di Barletta MR, Varnous S, Becane HM, Hammouda EH, Merlini L, Muntoni F, Greenberg CR, Gary F, Urtizberea JA, Duboc D, Fardeau M, Toniolo D, Schwartz K. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 1999;21:285-8.
-
(1999)
Nat Genet
, vol.21
, pp. 285-288
-
-
Bonne, G.1
Di Barletta, M.R.2
Varnous, S.3
Becane, H.M.4
Hammouda, E.H.5
Merlini, L.6
Muntoni, F.7
Greenberg, C.R.8
Gary, F.9
Urtizberea, J.A.10
Duboc, D.11
Fardeau, M.12
Toniolo, D.13
Schwartz, K.14
-
17
-
-
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, Lavergne T, Fardeau M, Eymard B, Weber S, Schwartz K, Duboc D. High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation. Pacing Clin Electrophysiol 2000;23:1661-6.
-
(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
Lavergne, T.8
Fardeau, M.9
Eymard, B.10
Weber, S.11
Schwartz, K.12
Duboc, D.13
-
18
-
-
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, Vidaillet HJ Jr, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Muehle G, Johnson W, McDonough B. 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;341:1715-24.
-
(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
Vidaillet H.J., Jr.8
Spudich, S.9
De Girolami, U.10
Seidman, J.G.11
Seidman, C.12
Muntoni, F.13
Muehle, G.14
Johnson, W.15
McDonough, B.16
-
19
-
-
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, Scelsi L, Baldini E, Gavazzi A, Tavazzi L. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease. J Am Coll Cardiol 2002;39:981-90.
-
(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
Scelsi, L.8
Baldini, E.9
Gavazzi, A.10
Tavazzi, L.11
-
20
-
-
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;144:1081-6.
-
(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
-
21
-
-
0034820958
-
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
-
Jakobs, PM, Hanson EL, Crispell KA, Toy W, Keegan H, Schilling K, Icenogle TB, Litt M, Hershberger RE. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease. J Card Fail 2001;7:249-56.
-
(2001)
J Card Fail
, vol.7
, pp. 249-256
-
-
Jakobs, P.M.1
Hanson, E.L.2
Crispell, K.A.3
Toy, W.4
Keegan, H.5
Schilling, K.6
Icenogle, T.B.7
Litt, M.8
Hershberger, R.E.9
-
22
-
-
0035256432
-
A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy
-
Genschel, J, Bochow B, Kuepferling S, Ewert R, Hetzer R, Lochs H, Schmidt H. A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy. Hum Mutat 2000;17:154.
-
(2000)
Hum Mutat
, vol.17
, pp. 154
-
-
Genschel, J.1
Bochow, B.2
Kuepferling, S.3
Ewert, R.4
Hetzer, R.5
Lochs, H.6
Schmidt, H.7
-
23
-
-
0034266107
-
A new frameshift mutation at codon 466 (1397delA) within the LMNA gene
-
Genschel J, Baier P, Kuepferling S, Proepsting MJ, Buettner C, Ewert R, Hetzer R, Lochs H, Schmidt HH. A new frameshift mutation at codon 466 (1397delA) within the LMNA gene. Hum Mutat 2000;16:278.
-
(2000)
Hum Mutat
, vol.16
, pp. 278
-
-
Genschel, J.1
Baier, P.2
Kuepferling, S.3
Proepsting, M.J.4
Buettner, C.5
Ewert, R.6
Hetzer, R.7
Lochs, H.8
Schmidt, H.H.9
-
24
-
-
0037405331
-
Functional consequences of an LMNA mutation associated with a new cardiac and non cardiac phenotype
-
Charniot J, Pascal C, Bouchier C, Sébillon P, Salama J, Duboscq-Bidot L, Peuchmaurd M, Desnos M, Artigou J, Komajda M. Functional consequences of an LMNA mutation associated with a new cardiac and non cardiac phenotype. Hum Mutat 2003;21:473-81.
-
(2003)
Hum Mutat
, vol.21
, pp. 473-481
-
-
Charniot, J.1
Pascal, C.2
Bouchier, C.3
Sébillon, P.4
Salama, J.5
Duboscq-Bidot, L.6
Peuchmaurd, M.7
Desnos, M.8
Artigou, J.9
Komajda, M.10
-
25
-
-
0035696932
-
Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy
-
Raharjo WH, Enarson P, Sullivan T, Stewart CL, Burke B. Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy. J Cell Sci 2001;114:4447-57.
-
(2001)
J Cell Sci
, vol.114
, pp. 4447-4457
-
-
Raharjo, W.H.1
Enarson, P.2
Sullivan, T.3
Stewart, C.L.4
Burke, B.5
-
26
-
-
0035697055
-
Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy
-
Ostlund C, Bonne G, Schwartz K, Worman HJ. Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy. J Cell Sci 2001;114:4435-45.
-
(2001)
J Cell Sci
, vol.114
, pp. 4435-4445
-
-
Ostlund, C.1
Bonne, G.2
Schwartz, K.3
Worman, H.J.4
-
27
-
-
0035691915
-
Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene
-
Vigouroux C, Auclair M, Dubosclard E, Pouchelet M, Capeau J, Courvalin JC, Buendia B. Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene. J Cell Sci 2001;114:4459-68.
-
(2001)
J Cell Sci
, vol.114
, pp. 4459-4468
-
-
Vigouroux, C.1
Auclair, M.2
Dubosclard, E.3
Pouchelet, M.4
Capeau, J.5
Courvalin, J.C.6
Buendia, B.7
-
28
-
-
0037225049
-
Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy
-
Favreau C, Dubosclard E, Ostlund C, Vigouroux C, Capeau J, Wehnert M, Higuet D, Worman HJ, Courvalin JC, Buendia B. Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy. Exp Cell Res 2003;282:14-23.
-
(2003)
Exp Cell Res
, vol.282
, pp. 14-23
-
-
Favreau, C.1
Dubosclard, E.2
Ostlund, C.3
Vigouroux, C.4
Capeau, J.5
Wehnert, M.6
Higuet, D.7
Worman, H.J.8
Courvalin, J.C.9
Buendia, B.10
-
29
-
-
0033494355
-
Familial dilated cardiomyopathy: Clinical features in French families
-
Mangin L, Charron P, Tesson F, Mallet A, Dubourg O, Desnos M, Benaische A, Gayet C, Gibelin P, Davy JM, Bonnet J, Sidi D, Schwartz K, Komaida M. Familial dilated cardiomyopathy: clinical features in French families. Eur J Heart Fail 1999;1:353-61.
-
(1999)
Eur J Heart Fail
, vol.1
, pp. 353-361
-
-
Mangin, L.1
Charron, P.2
Tesson, F.3
Mallet, A.4
Dubourg, O.5
Desnos, M.6
Benaische, A.7
Gayet, C.8
Gibelin, P.9
Davy, J.M.10
Bonnet, J.11
Sidi, D.12
Schwartz, K.13
Komaida, M.14
-
30
-
-
0033165780
-
Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity
-
Heart Muscle Disease Study Group
-
Mestroni L, Rocco C, Gregori D, Sinagra G, Di Lenarda A, Miocic S, Vatta M, Pinamonti B, Muntoni F, Caforio AL, McKenna WJ, Falaschi A, Giacca M, Camerini. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. J Am Coll Cardiol 1999;34:181-90.
-
(1999)
J Am Coll Cardiol
, vol.34
, pp. 181-190
-
-
Mestroni, L.1
Rocco, C.2
Gregori, D.3
Sinagra, G.4
Di Lenarda, A.5
Miocic, S.6
Vatta, M.7
Pinamonti, B.8
Muntoni, F.9
Caforio, A.L.10
McKenna, W.J.11
Falaschi, A.12
Giacca, M.13
Camerini14
-
31
-
-
0032934453
-
Cardiomyopathy ObotcrgotEHaCMPoFD. Guidelines for the study of familial dilated cardiomyopathies
-
Mestroni L, Maisch B, McKenna WJ, Schwartz K, Charron P, Rocco C, Tesson F, Richter A, Wilke A, Komajda M, Cardiomyopathy ObotcrgotEHaCMPoFD. Guidelines for the study of familial dilated cardiomyopathies. Eur Heart J 1999;20:93-102.
-
(1999)
Eur Heart J
, vol.20
, pp. 93-102
-
-
Mestroni, L.1
Maisch, B.2
McKenna, W.J.3
Schwartz, K.4
Charron, P.5
Rocco, C.6
Tesson, F.7
Richter, A.8
Wilke, A.9
Komajda, M.10
-
32
-
-
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, Urtizberea A, Becane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Ann Neurol 2000;48:170-80.
-
(2000)
Ann Neurol
, vol.48
, pp. 170-180
-
-
Bonne, G.1
Mercuri, E.2
Muchir, A.3
Urtizberea, A.4
Becane, H.M.5
Recan, D.6
Merlini, L.7
Wehnert, M.8
Boor, R.9
Reuner, U.10
Vorgerd, M.11
Wicklein, E.M.12
Eymard, B.13
Duboc, D.14
Penisson-Besnier, I.15
Cuisset, J.M.16
Ferrer, X.17
Desguerre, I.18
Lacombe, D.19
Bushby, K.20
Pollitt, C.21
Toniolo, D.22
Fardeau, M.23
Schwartz, K.24
Muntoni, F.25
more..
-
33
-
-
0033730389
-
Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy
-
Tesson F, Sylvius N, Pilotto A, Dubosq-Bidot L, Peuchmaurd M, Bouchier C, Benaiche A, Mangin L, Charron P, Gavazzi A, Tavazzi L, Arbustini E, Komajda M. Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy. Eur Heart J 2000;21:1872-6.
-
(2000)
Eur Heart J
, vol.21
, pp. 1872-1876
-
-
Tesson, F.1
Sylvius, N.2
Pilotto, A.3
Dubosq-Bidot, L.4
Peuchmaurd, M.5
Bouchier, C.6
Benaiche, A.7
Mangin, L.8
Charron, P.9
Gavazzi, A.10
Tavazzi, L.11
Arbustini, E.12
Komajda, M.13
-
34
-
-
0034620567
-
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
-
Brodsky G, 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;101:473-6.
-
(2000)
Circulation
, vol.101
, pp. 473-476
-
-
Brodsky, G.1
Muntoni, F.2
Miocic, S.3
Sinagra, G.4
Sewry, C.5
Mestroni, L.6
-
35
-
-
0030963540
-
Tachycardia-induced cardiomyopathy: A review of animal models and clinical studies
-
Shinbane JS, Wood MA, Jensen DN, Ellenbogen KA, Fitzpatrick AP, Scheinman MM. Tachycardia-induced cardiomyopathy: a review of animal models and clinical studies. J Am Coll Cardiol 1997;29:709-15.
-
(1997)
J Am Coll Cardiol
, vol.29
, pp. 709-715
-
-
Shinbane, J.S.1
Wood, M.A.2
Jensen, D.N.3
Ellenbogen, K.A.4
Fitzpatrick, A.P.5
Scheinman, M.M.6
-
36
-
-
0033912260
-
Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C
-
Speckman RA, Garg A, Du F, Bennett L, Veile R, Arioglu E, Taylor SI, Lovett M, Bowcock AM. Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C. Am J Hum Genet 2000;66:1192-8.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1192-1198
-
-
Speckman, R.A.1
Garg, A.2
Du, F.3
Bennett, L.4
Veile, R.5
Arioglu, E.6
Taylor, S.I.7
Lovett, M.8
Bowcock, A.M.9
-
37
-
-
0033082394
-
RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer
-
Culbertson MR. RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer. Trends Genet 1999;15:74-80.
-
(1999)
Trends Genet
, vol.15
, pp. 74-80
-
-
Culbertson, M.R.1
|