-
4
-
-
0020974404
-
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes
-
(1983)
J Neurol Sci
, vol.62
, pp. 327-355
-
-
Barth, P.G.1
Scholte, H.R.2
Berden, J.A.3
Van der Klei Van Moorsel, J.M.4
Luyt Houwen, I.E.5
Van't Veer Korthof, E.T.6
Van der Harten, J.J.7
Sobotka Plojhar, M.A.8
-
7
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
(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
-
8
-
-
0029784361
-
Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23
-
(1996)
J Clin Invest
, vol.98
, pp. 1355-1360
-
-
Bowles, K.R.1
Gajarski, R.2
Porter, P.3
Goytia, V.4
Bachinski, L.5
Roberts, R.6
Pignatelli, R.7
Towbin, J.A.8
-
13
-
-
16944366521
-
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
-
(1997)
Am J Hum Genet
, vol.61
, pp. 862-867
-
-
D'Adamo, P.1
Fassone, L.2
Gedeon, A.3
Janssen, E.A.M.4
Bione, S.5
Bolhuis, P.A.6
Barth, P.G.7
Wilson, M.8
Haan, E.9
Öratavik, K.H.10
Patton, M.A.11
Green, A.J.12
Zammarchi, E.13
Donati, M.A.14
Toniolo, D.15
-
16
-
-
0028801254
-
Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32
-
(1995)
Circulation
, vol.92
, pp. 3387-3389
-
-
Durand, J.B.1
Bachinski, L.L.2
Bieling, L.C.3
Czernuszewicz, G.Z.4
Abchee, A.B.5
Yu, Q.T.6
Tapscott, T.7
Hill, R.8
Ifegwu, J.9
Marian, A.J.10
Brugada, R.11
Daiger, S.12
Gregoritsch, J.M.13
Anderson, J.L.14
Quinones, M.15
Towbin, J.A.16
Roberts, R.17
-
18
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
(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.E.12
Muntoni, F.13
Muehle, G.14
Johnson, W.15
McDonough, B.16
-
19
-
-
0034643399
-
Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy
-
(2000)
N Engl J Med
, vol.342
, pp. 1077-1084
-
-
Felker, G.M.1
Thompson, R.E.2
Hare, J.M.3
Hruban, R.H.4
Clemetson, D.E.5
Howard, D.L.6
Baughman, K.L.7
Kasper, E.K.8
-
20
-
-
0343963762
-
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy
-
(2000)
Lancet
, vol.355
, pp. 1781-1785
-
-
Franz, W.M.1
Müller, M.2
Müller, O.J.3
Herrmann, R.4
Rothmann, Th.5
Cremer, M.6
Cohn, R.D.7
Voit, Th.8
Katus, H.A.9
-
21
-
-
17344373157
-
Missense mutations in desmin associated with familial cardiac and skeletal myopathy
-
(1998)
Nat Genet
, vol.19
, pp. 402-403
-
-
Goldfarb, L.G.1
Park, K.Y.2
Cervenakova, L.3
Gorokhova, S.4
Lee, H.S.5
Vasconcelos, O.6
Nagle, J.W.7
Semino Mora, C.8
Sivakumar, K.9
Dalakas, M.C.10
-
26
-
-
0025957444
-
Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy
-
(1991)
Lancet
, vol.337
, pp. 234-235
-
-
Ino, H.1
Tanaka, M.2
Ohno, K.3
Hattori, K.4
Ikebe, S.5
Sano, T.6
Ozawa, T.7
Ichiki, T.8
Kobayashi, M.9
Wada, Y.10
-
27
-
-
0033358083
-
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1068-1077
-
-
Jung, M.1
Poepping, I.2
Perrot, A.3
Ellmer, A.E.4
Wienker, Th.F.5
Dietz, R.6
Reis, A.7
Osterziel, K.J.8
-
28
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
(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
Jarcho, J.13
Shapiro, L.R.14
-
29
-
-
0028145745
-
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1
-
(1994)
Nature Genetics
, vol.7
, pp. 546-551
-
-
Kass, S.1
MacRae, C.2
Graber, H.L.3
Sparks, E.A.4
McNamara, D.5
Boudoulas, H.6
Basson, C.T.7
Baker III, P.B.8
Cody, R.J.9
Fishman, M.C.10
Cox, N.11
Kong, A.12
Wooley, C.F.13
Seidman, J.G.14
Seidman, C.E.15
-
32
-
-
0029151478
-
Linkage of familial dilated cardiomyopathy to chromosome 9
-
(1995)
Am J Hum Genet
, vol.57
, pp. 846-852
-
-
Krajinovic, M.1
Pinamonti, B.2
Sinagra, G.3
Vatta, M.4
Severini, M.5
Milasin, J.6
Falaschi, A.7
Camerini, F.8
Giacca, M.9
Mestroni, L.10
-
33
-
-
0033520037
-
Desmin mutation responsible for idiopathic dilated cardiomyopathy
-
(1999)
Circulation
, vol.100
, pp. 461-464
-
-
Li, D.1
Tapscoft, T.2
Gonzalez, O.3
Burch, 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
-
34
-
-
0034711772
-
Enteroviral capsid protein VP1 is present in myocardial tissues from some patients with myocarditis or dilated cardiomyopathy
-
(2000)
Circulation
, vol.101
, pp. 231-234
-
-
Li, Y.1
Bourlet, T.2
Andreoletti, L.3
Mosnier, J.F.4
Peng, T.5
Yang, Y.6
Archard, L.C.7
Pozzetto, B.8
Zhang, H.9
-
35
-
-
0026629099
-
Prevalence and etiology of idiopathic dilated cardiomyopathy (Summary of a National Heart, Lung, and Blood Institute Workshop)
-
(1992)
Am J Cardiol
, vol.69
, pp. 1458-1466
-
-
Manolio, T.A.1
Baughman, K.L.2
Rohdeffer, R.3
Pearson, T.A.4
Bristow, J.D.5
Michels, V.V.6
Abelmann, W.H.7
Harlan, W.R.8
-
38
-
-
0032934453
-
Guidelines for the study of familial dilated cardiomyopathies
-
(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
-
39
-
-
0033165780
-
Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity
-
(1999)
Journal of American College of Cardiology
, vol.34
, pp. 181-190
-
-
Mestroni, L.1
Rocco, Ch.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.P.10
McKenna, W.J.11
Falaschi, A.12
Giacca, M.13
Camerini, F.14
-
40
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
(1992)
N Engl J Med
, vol.326
, pp. 77-82
-
-
Michels, V.V.1
Moll, P.P.2
Miller, F.A.3
Tajik, J.4
Chu, J.S.5
Driscoll, D.J.6
Burnett, J.C.7
Rodeheffer, R.J.8
Chesebro, J.H.9
Tazelaar, H.10
-
41
-
-
0030028518
-
A point mutation in the 5′ splice site of the dystrophin gene first intron responsible for X-Linked dilated cardiomyopathy
-
(1996)
Human Molecular Genetics
, vol.5
, pp. 73-79
-
-
Milasin, J.1
Muntoni, F.2
Severin, G.M.3
Bartoloni, L.4
Vatta, M.5
Krajinovic, M.6
Mateddu, A.7
Angelini, C.8
Camerini, F.9
Falaschi, A.10
Mestroni, L.11
Giacca, M.12
-
42
-
-
0032751526
-
The absence of desmin leads to cardiomyocyte hypertrophy and cardiac dilation with compromised systolic function
-
(1999)
J Mol Cell Cardiol
, vol.31
, pp. 2063-2076
-
-
Milner, D.J.1
Taffet, G.E.2
Wang, X.3
Pham, T.4
Tamura, T.5
Hartley, C.6
Gerdes, A.M.7
Capetanaki, Y.8
-
44
-
-
0027265702
-
Brief report: Deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy
-
(1993)
N Engl J Med
, vol.329
, pp. 921-925
-
-
Muntoni, F.1
Cau, M.2
Ganau, A.3
Congiu, R.4
Arvedi, G.5
Mateddu, A.6
Marrosu, M.G.7
Cianchetti, C.8
Melis, M.A.9
-
46
-
-
0020535878
-
Prospective study of X-linked progressive muscular dystrophy in Campania
-
(1983)
Muscle Nerve
, vol.6
, pp. 253-262
-
-
Nigro, G.1
Comi, L.I.2
Limongelli, F.M.3
Giugliano, M.A.4
Politano, L.5
Petretta, V.6
Passamano, L.7
Stefanelli, S.8
-
50
-
-
0026781879
-
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1150-1155
-
-
Passos-Bueno, M.R.1
Bakker, E.2
Kneppers, A.L.3
Takata, R.I.4
Rapaport, D.5
Den Dunnen, J.T.6
Zatz, M.7
Van Ommen, G.J.8
-
52
-
-
0029971310
-
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies
-
(1996)
JAMA
, vol.275
, pp. 1335-1338
-
-
Politano, L.1
Nigro, V.2
Nigro, G.3
Petretta, V.R.4
Passamano, L.5
Papparella, S.6
Di Somma, S.7
Comi, L.I.8
-
53
-
-
0033927867
-
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive emery-dreifuss muscular dystrophy
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1407-1412
-
-
Raffaele Di Barletta, M.1
Ricci, E.2
Galluzzi, G.3
Tonali, P.4
Mora, M.5
Morandi, L.6
Romorini, A.7
Voit, T.8
Orstavik, K.H.9
Merlini, L.10
Trevisan, C.11
Biancalana, V.12
Housmanowa-Petrusewicz, I.13
Bione, S.14
Ricotti, R.15
Schwartz, K.16
Bonne, G.17
Toniolo, D.18
-
55
-
-
0029864693
-
Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of Cardiomyopathies
-
(1996)
Circulation
, vol.93
, pp. 841-842
-
-
Richardson, P.1
McKenna, W.2
Bristow, M.3
Maisch, B.4
Mautner, B.5
O'Connell, J.6
Olsen, E.7
Thiene, G.8
Goodwin, J.9
Gyarfas, I.10
Martin, I.11
Nordet, P.12
-
58
-
-
0343183359
-
Dilated cardiomyopathy and sensorineural hearing loss: A heritable syndrome that maps to 6q23-24
-
(2000)
Circulation
, vol.101
, pp. 1812-1818
-
-
Schönberger, J.1
Levy, H.2
Grünig, E.3
Sangwatanaroj, S.4
Fatkin, D.5
MacRae, C.6
Stacker, H.7
Halpin, C.8
Eavey, R.9
Philbin, E.F.10
Katus, H.11
Seidman, J.G.12
Seidman, C.E.13
-
61
-
-
0033514986
-
Familial dilated cardiomyopathy locus maps to chromosome 2q31
-
(1999)
Circulation
, vol.99
, pp. 1022-1026
-
-
Siu, B.L.1
Niimura, H.2
Osborne, J.A.3
Fatkin, D.4
MacRae, C.5
Solomon, S.6
Benson, D.W.7
Seidman, J.G.8
Seidman, C.E.9
-
64
-
-
0035168177
-
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16
-
(2000)
Am J Hum Genet
, vol.68
, pp. 241-246
-
-
Sylvius, N.1
Tesson, F.2
Gayet, C.3
Charron, P.4
Benaiche, A.5
Peuchmaurd, M.6
Duboscq-Bidot, L.7
Feingold, J.8
Beckmann, J.S.9
Bouchier, C.10
Komajda, M.11
-
65
-
-
0026660498
-
Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy
-
(1992)
Biochem Biophys Res Commun
, vol.186
, pp. 47-53
-
-
Taniike, M.1
Fukushima, H.2
Yanagihara, I.3
Tsukamoto, H.4
Tanaka, J.5
Fujimura, H.6
Nagai, T.7
Sano, T.8
Yamaoka, K.9
Inui, K.10
-
66
-
-
0032600356
-
Prognose der linksventrikulären dysfunktion 1998 in einem nichtuniversitären krankenhaus der maximalversorgung
-
(1999)
Z Kardiol
, vol.88
, pp. 14-22
-
-
Taubert, G.1
Kottmann, T.2
Gitt, A.K.3
Winkler, R.4
Bergmeier, C.5
Kleemann, T.6
Seidl, K.7
Senges, J.8
-
67
-
-
0033730389
-
Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy
-
(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
-
68
-
-
0027193330
-
X-linked dilated cardiomyopathy: Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
-
(1993)
Circulation
, vol.87
, pp. 1854-1865
-
-
Towbin, J.A.1
Hejtmancik, J.F.2
Brink, P.3
Gelb, B.4
Zhu, X.M.5
Chamberlain, J.S.6
McCabe, E.R.B.7
Swift, M.8
-
70
-
-
0033818186
-
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
-
(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
-
72
-
-
0025807222
-
Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA (Leu) (UUR)
-
(1991)
Lancet
, vol.338
, pp. 143-147
-
-
Zeviani, M.1
Gellera, C.2
Antozzi, C.3
Rimoldi, M.4
Morandi, L.5
Villani, F.6
Tiranti, V.7
DiDonato, S.8
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