-
1
-
-
0029864693
-
Report of the 1995 World Health Organization/ International Society and Federation of Cardiology task force on the definition and classification of cardiomyopathies
-
(1995)
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
-
2
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
(1992)
New 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
-
4
-
-
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
-
5
-
-
0027265702
-
Deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy
-
(1993)
New Eng. 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
Realdi, G.9
Cao, A.10
-
6
-
-
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
-
7
-
-
0034326902
-
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2761-2766
-
-
Norgett, E.E.1
Hatsell, S.J.2
Carvajal-Huerta, L.3
Cabezas, J.C.4
Common, J.5
Purkis, P.E.6
Whittock, N.7
Leigh, I.M.8
Stevens, H.P.9
Kelsell, D.P.10
-
8
-
-
0034679297
-
Identification of a deletion in plako-globin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
-
(2000)
Lancet
, vol.355
, pp. 2119-2124
-
-
McKoy, G.1
Protonotarios, N.2
Crosby, A.3
Tsatsopoulou, A.4
Anastasakis, A.5
Coonar, A.6
Norman, M.7
Baboonian, C.8
Jeffery, S.9
McKenna, W.J.10
-
9
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
(2000)
New Eng. 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
-
10
-
-
0030905471
-
Carnitine palmitoyltransferase in patients with cardiac ischemia due to atherosclerotic coronary artery disease and in patients with idiopathic dilated cardiomyopathy
-
(1997)
Cardiology
, vol.88
, pp. 258-263
-
-
Maurer, I.1
Zierz, S.2
-
12
-
-
0029874852
-
Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy
-
(1996)
Nature Genet.
, vol.12
, pp. 254-259
-
-
Nagano, A.1
Koga, R.2
Ogawa, M.3
Kurano, Y.4
Kawada, J.5
Okada, R.6
Hayashi, Y.K.7
Tsukahara, T.8
Arahata, K.9
-
13
-
-
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.8
Spudich, S.9
De Girolami, U.10
-
15
-
-
0030933063
-
MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure
-
(1997)
Cell
, vol.88
, pp. 393-403
-
-
Arber, S.1
Hunter, J.J.2
Ross, J.3
Hongo, M.4
Sansig, G.5
Borg, J.6
Perriard, J.C.7
Chien, K.R.8
Caroni, P.9
-
16
-
-
0035033212
-
Adult mice deficient in actinin-associated LIM-domain protein reveal a developmental pathway for right ventricular cardiomyopathy
-
(2001)
Nat. Med.
, vol.7
, pp. 591-597
-
-
Pashmforoush, M.1
Pomies, P.2
Peterson, K.L.3
Kubalak, S.4
Ross, J.5
Hefti, A.6
Aebi, U.7
Beckerle, M.C.8
Chien, K.R.9
-
17
-
-
0031471956
-
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 13873-13878
-
-
Sakamoto, A.1
Ono, K.2
Abe, M.3
Jasmin, G.4
Eki, T.5
Murakami, Y.6
Masaki, T.7
Toyo-oka, T.8
Hanaoka, F.9
-
20
-
-
0035941407
-
The complete gene sequence of titin, expression of an unusual -700 kDa titin isoform and its interaction with obscurin identify a novel Z-line to I-band linking system
-
(2001)
Circ. Res.
, vol.89
, pp. 1065-1071
-
-
Bang, M.L.1
Centner, T.2
Fornoff, F.3
Geach, A.J.4
Gotthardt, M.5
McNabb, M.6
Witt, C.C.7
Labeit, D.8
Gregorio, C.C.9
Granzier, H.10
-
21
-
-
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
-
23
-
-
0035936792
-
The genetic basis for cardiomyopathy: From mutation identification to manifestation paradigms
-
(2001)
Cell
, vol.104
, pp. 557-567
-
-
Seidman, J.G.1
Seidman, C.2
-
25
-
-
0031213849
-
Tissue-specific expression and α-actinin binding properties of the Z-disc titin: Implications for the nature of vertebrate Z-discs
-
(1997)
J. Mol. Biol.
, vol.270
, pp. 688-695
-
-
Sorimachi, H.1
Freiburg, A.2
Kolmerer, B.3
Ishiura, S.4
Stier, G.5
Gregorio, C.C.6
Labeit, D.7
Linke, W.A.8
Suzuki, K.9
Labeit, S.10
-
28
-
-
0032538660
-
The NH2 terminus of titin spans the Z-disc: Its interaction with a novel 19-kD ligand (T-cap) is required for sarcomeric integrity
-
(1998)
J. Cell Biol.
, vol.143
, pp. 1013-1027
-
-
Gregorio, C.C.1
Trombitas, K.2
Centner, T.3
Kolmerer, B.4
Stier, G.5
Kunke, K.6
Suzuki, K.7
Obermayr, F.8
Herrmann, B.9
Granzier, H.10
-
29
-
-
0031590316
-
Telethonin, a novel sarcomeric protein of heart and skeletal muscle
-
(1997)
FEBS Lett.
, vol.415
, pp. 163-168
-
-
Valle, G.1
Faulkner, G.2
De Antoni, A.3
Pacchioni, B.4
Pallavicini, A.5
Pandolfo, D.6
Tiso, N.7
Toppo, S.8
Trevisan, S.9
Lanfranchi, G.10
-
30
-
-
0032578901
-
Structural basis for activation of the titin kinase domain during myofibril-logenesis
-
(1998)
Nature
, vol.395
, pp. 863-869
-
-
Mayans, O.1
Van der Ven, P.F.2
Wilm, M.3
Mues, A.4
Young, P.5
Furst, D.O.6
Wilmanns, M.7
Gautel, M.8
-
32
-
-
0028791482
-
DNA typing of HLA class II genes in Japanese patients with dilated cardiomyopathy
-
(1995)
J. Mol. Cell. Cardiol.
, vol.27
, pp. 2385-2392
-
-
Nishi, H.1
Koga, Y.2
Koyanagi, T.3
Harada, H.4
Imaizumi, T.5
Toshima, H.6
Sasazuki, T.7
Kimura, A.8
-
34
-
-
17744380992
-
Characterization of the human nebulette gene: A polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy
-
(2000)
Hum. Genet.
, vol.107
, pp. 440-451
-
-
Arimura, T.1
Nakamura, T.2
Hiroi, S.3
Satoh, M.4
Takahashi, M.5
Ohbuchi, N.6
Ueda, K.7
Nouchi, T.8
Yamaguchi, N.9
Akai, J.10
-
40
-
-
0032479445
-
Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 17073-17078
-
-
Ono, Y.1
Shimada, H.2
Sorimahi, H.3
Richard, I.4
Saido, T.C.5
Beckmann, J.S.6
Ishiura, S.7
Suzuki, K.8
-
41
-
-
0030920253
-
Dystrophinopathy, the expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy
-
(1997)
Circulation
, vol.95
, pp. 17-20
-
-
Beggs, A.H.1
-
43
-
-
0033729916
-
Genetics and dilated cardiomyopathy: Limitation of candidate gene strategies
-
(2000)
Eur. Heart J.
, vol.21
, pp. 1817-1819
-
-
MacRae, C.A.1
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