-
1
-
-
84883163817
-
Dilated cardiomyopathy: the complexity of a diverse genetic architecture
-
Hershberger RE, Hedges DJ, Morales A. Dilated cardiomyopathy: the complexity of a diverse genetic architecture. Nat Rev Cardiol 2013;10:531–547.
-
(2013)
Nat Rev Cardiol
, vol.10
, pp. 531-547
-
-
Hershberger, R.E.1
Hedges, D.J.2
Morales, A.3
-
2
-
-
84859218872
-
Genetic testing for dilated cardiomyopathy in clinical practice
-
Lakdawala NK, Funke BH, Baxter S, Cirino AL, Roberts AE, Judge DP, Johnson N, Mendelsohn NJ, Morel C, Care M, Chung WK, Jones C, Psychogios A, Duffy E, Rehm HL, White E, Seidman JG, Seidman CE, Ho CY. Genetic testing for dilated cardiomyopathy in clinical practice. J Card Fail 2012;18:296–303.
-
(2012)
J Card Fail
, vol.18
, pp. 296-303
-
-
Lakdawala, N.K.1
Funke, B.H.2
Baxter, S.3
Cirino, A.L.4
Roberts, A.E.5
Judge, D.P.6
Johnson, N.7
Mendelsohn, N.J.8
Morel, C.9
Care, M.10
Chung, W.K.11
Jones, C.12
Psychogios, A.13
Duffy, E.14
Rehm, H.L.15
White, E.16
Seidman, J.G.17
Seidman, C.E.18
Ho, C.Y.19
-
3
-
-
84863116641
-
Truncations of titin causing dilated cardiomyopathy
-
Herman DS, Lam L, Taylor MRGG, Wang L, Teekakirikul P, Christodoulou D, Conner L, DePalma SR, McDonough B, Sparks E, Teodorescu DL, Cirino AL, Banner NR, Pennell DJ, Graw S, Merlo M, Lenarda A Di, Sinagra G, Bos JM, Ackerman MJ, Mitchell RN, Murry CE, Lakdawala NK, Ho CY, Barton PJRR, Cook SA, Mestroni L, Seidman JGG, Seidman CE. Truncations of titin causing dilated cardiomyopathy. N Engl J Med 2012;366:619–628.
-
(2012)
N Engl J Med
, vol.366
, pp. 619-628
-
-
Herman, D.S.1
Lam, L.2
Taylor, M.R.G.G.3
Wang, L.4
Teekakirikul, P.5
Christodoulou, D.6
Conner, L.7
DePalma, S.R.8
McDonough, B.9
Sparks, E.10
Teodorescu, D.L.11
Cirino, A.L.12
Banner, N.R.13
Pennell, D.J.14
Graw, S.15
Merlo, M.16
Lenarda, A.D.17
Sinagra, G.18
Bos, J.M.19
Ackerman, M.J.20
Mitchell, R.N.21
Murry, C.E.22
Lakdawala, N.K.23
Ho, C.Y.24
Barton, P.J.R.R.25
Cook, S.A.26
Mestroni, L.27
Seidman, J.G.G.28
Seidman, C.E.29
more..
-
4
-
-
84876276624
-
Exome sequencing and genome-wide linkage analysis in 17 families illustrates the complex contribution of TTN truncating variants to dilated cardiomyopathy
-
Norton N, Li D, Rampersaud E, Morales A, Martin ER, Zuchner S, Guo S, Gonzalez M, Hedges DJ, Robertson PD, Krumm N, Nickerson D a, Hershberger RE. Exome sequencing and genome-wide linkage analysis in 17 families illustrates the complex contribution of TTN truncating variants to dilated cardiomyopathy. Circ Cardiovasc Genet 2013;6:144–153.
-
(2013)
Circ Cardiovasc Genet
, vol.6
, pp. 144-153
-
-
Norton, N.1
Li, D.2
Rampersaud, E.3
Morales, A.4
Martin, E.R.5
Zuchner, S.6
Guo, S.7
Gonzalez, M.8
Hedges, D.J.9
Robertson, P.D.10
Krumm, N.11
Nickerson, D.A.12
Hershberger, R.E.13
-
5
-
-
84906047643
-
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy
-
Spaendonck-Zwarts KY van, Posafalvi A, van den Berg MP, Hilfiker-Kleiner D, Bollen IAE, Sliwa K, Alders M, Almomani R, van Langen IM, van der Meer P, Sinke RJ, van der Velden J, Van Veldhuisen DJ, van Tintelen JP, Jongbloed JDH. Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy. Eur Heart J 2014;35:2165–2173.
-
(2014)
Eur Heart J
, vol.35
, pp. 2165-2173
-
-
van Spaendonck-Zwarts, K.Y.1
Posafalvi, A.2
van den Berg, M.P.3
Hilfiker-Kleiner, D.4
Bollen, I.A.E.5
Sliwa, K.6
Alders, M.7
Almomani, R.8
van Langen, I.M.9
van der Meer, P.10
Sinke, R.J.11
van der Velden, J.12
Van Veldhuisen, D.J.13
van Tintelen, J.P.14
Jongbloed, J.D.H.15
-
6
-
-
84906061711
-
A rising titan: TTN review and mutation update
-
Chauveau C, Rowell J, Ferreiro A. A rising titan: TTN review and mutation update. Hum Mutat 2014;35:1046–1059.
-
(2014)
Hum Mutat
, vol.35
, pp. 1046-1059
-
-
Chauveau, C.1
Rowell, J.2
Ferreiro, A.3
-
7
-
-
0033514986
-
Familial dilated cardiomyopathy locus maps to chromosome 2q31
-
Siu B, Niimura H, Osborne J, Fatkin D. Familial dilated cardiomyopathy locus maps to chromosome 2q31. Circulation 1999;99:1022–1027.
-
(1999)
Circulation
, vol.99
, pp. 1022-1027
-
-
Siu, B.1
Niimura, H.2
Osborne, J.3
Fatkin, D.4
-
8
-
-
0036478897
-
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
-
Gerull B, Gramlich M, Atherton J, McNabb M, Trombitás 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;30:201–204.
-
(2002)
Nat Genet
, vol.30
, pp. 201-204
-
-
Gerull, B.1
Gramlich, M.2
Atherton, J.3
McNabb, M.4
Trombitás, 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
-
9
-
-
18444408379
-
Titin mutations as the molecular basis for dilated cardiomyopathy
-
Itoh-Satoh M, Hayashi T, Nishi H, Koga Y, Arimura T, Koyanagi T, Takahashi M, Hohda S, Ueda K, Nouchi T, Hiroe M, Marumo F, Imaizumi T, Yasunami M, Kimura A. Titin mutations as the molecular basis for dilated cardiomyopathy. Biochem Biophys Res Commun 2002;291:385–393.
-
(2002)
Biochem Biophys Res Commun
, vol.291
, pp. 385-393
-
-
Itoh-Satoh, M.1
Hayashi, T.2
Nishi, H.3
Koga, Y.4
Arimura, T.5
Koyanagi, T.6
Takahashi, M.7
Hohda, S.8
Ueda, K.9
Nouchi, T.10
Hiroe, M.11
Marumo, F.12
Imaizumi, T.13
Yasunami, M.14
Kimura, A.15
-
10
-
-
33744495726
-
Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy
-
Gerull B, Atherton J, Geupel A, Sasse-Klaassen S, Heuser A, Frenneaux M, McNabb M, Granzier H, Labeit S, Thierfelder L. Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy. J Mol Med 2006;84:478–483.
-
(2006)
J Mol Med
, vol.84
, pp. 478-483
-
-
Gerull, B.1
Atherton, J.2
Geupel, A.3
Sasse-Klaassen, S.4
Heuser, A.5
Frenneaux, M.6
McNabb, M.7
Granzier, H.8
Labeit, S.9
Thierfelder, L.10
-
11
-
-
0028957373
-
Passive tension in cardiac muscle: contribution of collagen, titin, microtubules, and intermediate filaments
-
Granzier HL, Irving TC. Passive tension in cardiac muscle: contribution of collagen, titin, microtubules, and intermediate filaments. Biophys J 1995;68:1027–1044.
-
(1995)
Biophys J
, vol.68
, pp. 1027-1044
-
-
Granzier, H.L.1
Irving, T.C.2
-
12
-
-
84892953505
-
Recessive TTN truncating mutations define novel forms of core myopathy with heart disease
-
Chauveau C, Bonnemann CG, Julien C, Kho AL, Marks H, Talim B, Maury P, Arne-Bes MC, Uro-Coste E, Alexandrovich A, Vihola A, Schafer S, Kaufmann B, Medne L, Hübner N, Foley a. R, Santi M, Udd B, Topaloglu H, Moore SA., Gotthardt M, Samuels ME, Gautel M, Ferreiro A. Recessive TTN truncating mutations define novel forms of core myopathy with heart disease. Hum Mol Genet 2014;23:980–991.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 980-991
-
-
Chauveau, C.1
Bonnemann, C.G.2
Julien, C.3
Kho, A.L.4
Marks, H.5
Talim, B.6
Maury, P.7
Arne-Bes, M.C.8
Uro-Coste, E.9
Alexandrovich, A.10
Vihola, A.11
Schafer, S.12
Kaufmann, B.13
Medne, L.14
Hübner, N.15
Foley a, R.16
Santi, M.17
Udd, B.18
Topaloglu, H.19
Moore, S.A.20
Gotthardt, M.21
Samuels, M.E.22
Gautel, M.23
Ferreiro, A.24
more..
-
13
-
-
84867824466
-
Population-based variation in cardiomyopathy genes
-
Golbus JR, Puckelwartz MJ, Fahrenbach JP, Dellefave-castillo LM, Wolfgeher D, Mcnally EM. Population-based variation in cardiomyopathy genes. Circ Cardiovasc Genet 2012;5:391–399.
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 391-399
-
-
Golbus, J.R.1
Puckelwartz, M.J.2
Fahrenbach, J.P.3
Dellefave-castillo, L.M.4
Wolfgeher, D.5
Mcnally, E.M.6
-
14
-
-
84988449067
-
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
-
Roberts AM, Ware JS, Herman DS, Schafer S, Baksi J, Bick AG, Buchan RJ, Walsh R, John S, Wilkinson S, Mazzarotto F, Felkin LE, Gong S, L. MacArthur JA, Cunningham F, Flannick J, Gabriel SB, Altshuler DM, Macdonald PS, Heinig M, Keogh AM, Hayward CS, Banner NR, Pennell DJ, O'Regan DP, San TR, de Marvao A, Dawes TJ, Gulati A, Birks EJ, Yacoub MH, Radke M, Gotthardt M, Wilson JG, O'Donnell CJ, Prasad SK, R Barton PJ, Fatkin D, Hubner N, Seidman JG, Seidman CE, Cook SA. Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. Sci Transl Med 2015;7:270ra6.
-
(2015)
Sci Transl Med
, vol.7
, pp. 270ra6
-
-
Roberts, A.M.1
Ware, J.S.2
Herman, D.S.3
Schafer, S.4
Baksi, J.5
Bick, A.G.6
Buchan, R.J.7
Walsh, R.8
John, S.9
Wilkinson, S.10
Mazzarotto, F.11
Felkin, L.E.12
Gong, S.L.13
MacArthur, J.A.14
Cunningham, F.15
Flannick, J.16
Gabriel, S.B.17
Altshuler, D.M.18
Macdonald, P.S.19
Heinig, M.20
Keogh, A.M.21
Hayward, C.S.22
Banner, N.R.23
Pennell, D.J.24
O'Regan, D.P.25
San, T.R.26
de Marvao, A.27
Dawes, T.J.28
Gulati, A.29
Birks, E.J.30
Yacoub, M.H.31
Radke, M.32
Gotthardt, M.33
Wilson, J.G.34
O'Donnell, C.J.35
Prasad, S.K.R.36
Barton, P.J.37
Fatkin, D.38
Hubner, N.39
Seidman, J.G.40
Seidman, C.E.41
Cook, S.A.42
more..
-
15
-
-
84921047797
-
Tackling the Achilles' heel of genetic testing
-
Watkins H. Tackling the Achilles' heel of genetic testing. Sci Transl Med 2015;7:270fs1.
-
(2015)
Sci Transl Med
, vol.7
, pp. 270fs1
-
-
Watkins, H.1
-
16
-
-
84956904418
-
Prevalence of titin truncating variants in general population
-
Akinrinade O, Koskenvuo JW, Alastalo T-P. Prevalence of titin truncating variants in general population. PLoS One 2015;10:e0145284.
-
(2015)
PLoS One
, vol.10
-
-
Akinrinade, O.1
Koskenvuo, J.W.2
Alastalo, T.-P.3
-
17
-
-
84973594839
-
Relevance of truncating titin mutations in dilated cardiomyopathy
-
Akinrinade O, Alastalo T-P, Koskenvuo JW. Relevance of truncating titin mutations in dilated cardiomyopathy. Clin Genet 2016;90:49–54.
-
(2016)
Clin Genet
, vol.90
, pp. 49-54
-
-
Akinrinade, O.1
Alastalo, T.-P.2
Koskenvuo, J.W.3
-
18
-
-
84988366010
-
Shared genetic predisposition in peripartum and dilated cardiomyopathies
-
Ware JS, Li J, Mazaika E, Yasso CM, DeSouza T, Cappola TP, Tsai EJ, Hilfiker-Kleiner D, Kamiya CA, Mazzarotto F, Cook SA, Halder I, Prasad SK, Pisarcik J, Hanley-Yanez K, Alharethi R, Damp J, Hsich E, Elkayam U, Sheppard R, Kealey A, Alexis J, Ramani G, Safirstein J, Boehmer J, Pauly DF, Wittstein IS, Thohan V, Zucker MJ, Liu P, Gorcsan J, McNamara DM, Seidman CE, Seidman JG, Arany Z. Shared genetic predisposition in peripartum and dilated cardiomyopathies. N Engl J Med 2016;374:233–241.
-
(2016)
N Engl J Med
, vol.374
, pp. 233-241
-
-
Ware, J.S.1
Li, J.2
Mazaika, E.3
Yasso, C.M.4
DeSouza, T.5
Cappola, T.P.6
Tsai, E.J.7
Hilfiker-Kleiner, D.8
Kamiya, C.A.9
Mazzarotto, F.10
Cook, S.A.11
Halder, I.12
Prasad, S.K.13
Pisarcik, J.14
Hanley-Yanez, K.15
Alharethi, R.16
Damp, J.17
Hsich, E.18
Elkayam, U.19
Sheppard, R.20
Kealey, A.21
Alexis, J.22
Ramani, G.23
Safirstein, J.24
Boehmer, J.25
Pauly, D.F.26
Wittstein, I.S.27
Thohan, V.28
Zucker, M.J.29
Liu, P.30
Gorcsan, J.31
McNamara, D.M.32
Seidman, C.E.33
Seidman, J.G.34
Arany, Z.35
more..
-
19
-
-
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. 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
-
20
-
-
84884489700
-
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers
-
van Rijsingen IAW, Nannenberg EA, Arbustini E, Elliott PM, Mogensen J, Hermans-van Ast JF, van der Kooi AJ, van Tintelen JP, van den Berg MP, Grasso M, Serio A, Jenkins S, Rowland C, Richard P, Wilde AAM, Perrot A, Pankuweit S, Zwinderman AH, Charron P, Christiaans I, Pinto YM. Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers. Eur J Heart Fail 2013;15:376–384.
-
(2013)
Eur J Heart Fail
, vol.15
, pp. 376-384
-
-
van Rijsingen, I.A.W.1
Nannenberg, E.A.2
Arbustini, E.3
Elliott, P.M.4
Mogensen, J.5
Hermans-van Ast, J.F.6
van der Kooi, A.J.7
van Tintelen, J.P.8
van den Berg, M.P.9
Grasso, M.10
Serio, A.11
Jenkins, S.12
Rowland, C.13
Richard, P.14
Wilde, A.A.M.15
Perrot, A.16
Pankuweit, S.17
Zwinderman, A.H.18
Charron, P.19
Christiaans, I.20
Pinto, Y.M.21
more..
-
21
-
-
84878318267
-
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience
-
van Spaendonck-Zwarts KY, van Rijsingen IAW, van den Berg MP, Lekanne Deprez RH, Post JG, van Mil AM, Asselbergs FW, Christiaans I, van Langen IM, Wilde AAM, de Boer RA, Jongbloed JDH, Pinto YM, van Tintelen JP. Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. Eur J Heart Fail 2013;15:628–636.
-
(2013)
Eur J Heart Fail
, vol.15
, pp. 628-636
-
-
van Spaendonck-Zwarts, K.Y.1
van Rijsingen, I.A.W.2
van den Berg, M.P.3
Lekanne Deprez, R.H.4
Post, J.G.5
van Mil, A.M.6
Asselbergs, F.W.7
Christiaans, I.8
van Langen, I.M.9
Wilde, A.A.M.10
de Boer, R.A.11
Jongbloed, J.D.H.12
Pinto, Y.M.13
van Tintelen, J.P.14
-
22
-
-
0032934453
-
Guidelines for the study of familial dilated cardiomyopathies
-
Mestroni L, Maisch B. 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
-
23
-
-
84864477617
-
ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC
-
McMurray JJ, Adamopoulos S, Anker SD, Auricchio A, Bohm M, Dickstein K, Falk V, Filippatos G, Fonseca C, Gomez-Sanchez MA, Jaarsma T, Kober L, Lip GY, Maggioni AP, Parkhomenko A, Pieske BM, Popescu BA, Ronnevik PK, Rutten FH, Schwitter J, Seferovic P, Stepinska J, Trindade PT, Voors AA, Zannad F, Zeiher A, Bax JJ, Baumgartner H, Ceconi C, Dean V, Deaton C, Fagard R, Funck-Brentano C, Hasdai D, Hoes A, Kirchhof P, Knuuti J, Kolh P, McDonagh T, Moulin C, Reiner Z, Sechtem U, Sirnes PA, Tendera M, Torbicki A, Vahanian A, Windecker S, Bonet LA, Avraamides P, Ben Lamin HA, Brignole M, Coca A, Cowburn P, Dargie H, Elliott P, Flachskampf FA, Guida GF, Hardman S, Iung B, Merkely B, Mueller C, Nanas JN, Nielsen OW, Orn S, Parissis JT, Ponikowski P. ESC guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur J Heart Fail 2012;14:803–869.
-
(2012)
Eur J Heart Fail
, vol.14
, pp. 803-869
-
-
McMurray, J.J.1
Adamopoulos, S.2
Anker, S.D.3
Auricchio, A.4
Bohm, M.5
Dickstein, K.6
Falk, V.7
Filippatos, G.8
Fonseca, C.9
Gomez-Sanchez, M.A.10
Jaarsma, T.11
Kober, L.12
Lip, G.Y.13
Maggioni, A.P.14
Parkhomenko, A.15
Pieske, B.M.16
Popescu, B.A.17
Ronnevik, P.K.18
Rutten, F.H.19
Schwitter, J.20
Seferovic, P.21
Stepinska, J.22
Trindade, P.T.23
Voors, A.A.24
Zannad, F.25
Zeiher, A.26
Bax, J.J.27
Baumgartner, H.28
Ceconi, C.29
Dean, V.30
Deaton, C.31
Fagard, R.32
Funck-Brentano, C.33
Hasdai, D.34
Hoes, A.35
Kirchhof, P.36
Knuuti, J.37
Kolh, P.38
McDonagh, T.39
Moulin, C.40
Reiner, Z.41
Sechtem, U.42
Sirnes, P.A.43
Tendera, M.44
Torbicki, A.45
Vahanian, A.46
Windecker, S.47
Bonet, L.A.48
Avraamides, P.49
Ben Lamin, H.A.50
Brignole, M.51
Coca, A.52
Cowburn, P.53
Dargie, H.54
Elliott, P.55
Flachskampf, F.A.56
Guida, G.F.57
Hardman, S.58
Iung, B.59
Merkely, B.60
Mueller, C.61
Nanas, J.N.62
Nielsen, O.W.63
Orn, S.64
Parissis, J.T.65
Ponikowski, P.66
more..
-
24
-
-
84884294190
-
2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines
-
Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH, Fonarow GC, Geraci SA, Horwich T, Januzzi JL, Johnson MR, Kasper EK, Levy WC, Masoudi FA, McBride PE, McMurray JJV, Mitchell JE, Peterson PN, Riegel B, Sam F, Stevenson LW, Tang WHW, Tsai EJ, Wilkoff BL. 2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol 2013;62:e147–e239.
-
(2013)
J Am Coll Cardiol
, vol.62
, pp. e147-e239
-
-
Yancy, C.W.1
Jessup, M.2
Bozkurt, B.3
Butler, J.4
Casey, D.E.5
Drazner, M.H.6
Fonarow, G.C.7
Geraci, S.A.8
Horwich, T.9
Januzzi, J.L.10
Johnson, M.R.11
Kasper, E.K.12
Levy, W.C.13
Masoudi, F.A.14
McBride, P.E.15
McMurray, J.J.V.16
Mitchell, J.E.17
Peterson, P.N.18
Riegel, B.19
Sam, F.20
Stevenson, L.W.21
Tang, W.H.W.22
Tsai, E.J.23
Wilkoff, B.L.24
more..
-
25
-
-
84885022072
-
Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience
-
Hofman N, Tan HL, Alders M, Kolder I, De Haij S, Mannens MMAM, Lombardi MP, Dit Deprez RHL, Van Langen I, Wilde AAM. Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience. Circulation 2013;128:1513–1521.
-
(2013)
Circulation
, vol.128
, pp. 1513-1521
-
-
Hofman, N.1
Tan, H.L.2
Alders, M.3
Kolder, I.4
De Haij, S.5
Mannens, M.M.A.M.6
Lombardi, M.P.7
Dit Deprez, R.H.L.8
Van Langen, I.9
Wilde, A.A.M.10
-
26
-
-
84856194138
-
Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort study
-
R van ijsingen IAW, Arbustini E, Elliott PM, Mogensen J, Hermans-van Ast JF, van der Kooi AJ, van Tintelen JP, van den Berg MP, Pilotto A, Pasotti M, Jenkins S, Rowland C, Aslam U, Wilde AAM, Perrot A, Pankuweit S, Zwinderman AH, Charron P, Pinto YM. Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort study. J Am Coll Cardiol 2012;59:493–500.
-
(2012)
J Am Coll Cardiol
, vol.59
, pp. 493-500
-
-
R van ijsingen, I.A.W.1
Arbustini, E.2
Elliott, P.M.3
Mogensen, J.4
Hermans-van Ast, J.F.5
van der Kooi, A.J.6
van Tintelen, J.P.7
van den Berg, M.P.8
Pilotto, A.9
Pasotti, M.10
Jenkins, S.11
Rowland, C.12
Aslam, U.13
Wilde, A.A.M.14
Perrot, A.15
Pankuweit, S.16
Zwinderman, A.H.17
Charron, P.18
Pinto, Y.M.19
-
28
-
-
84941203449
-
Genetics and genotype–phenotype correlations in Finnish patients with dilated cardiomyopathy
-
Akinrinade O, Ollila L, Vattulainen S, Tallila J, Gentile M, Salmenperä P, Koillinen H, Kaartinen M, Nieminen MS, Myllykangas S, Alastalo TP, Koskenvuo JW, Heliö T. Genetics and genotype–phenotype correlations in Finnish patients with dilated cardiomyopathy. Eur Heart J 2015;36:2327–2337.
-
(2015)
Eur Heart J
, vol.36
, pp. 2327-2337
-
-
Akinrinade, O.1
Ollila, L.2
Vattulainen, S.3
Tallila, J.4
Gentile, M.5
Salmenperä, P.6
Koillinen, H.7
Kaartinen, M.8
Nieminen, M.S.9
Myllykangas, S.10
Alastalo, T.P.11
Koskenvuo, J.W.12
Heliö, T.13
-
29
-
-
84940491378
-
Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy
-
Hinson JT, Chopra A, Nafissi N, Polacheck WJ, Benson CC, Swist S, Gorham J, Yang L, Schafer S, Sheng CC, Haghighi A, Homsy J, Hubner N, Church G, Cook SA, Linke WA, Chen CS, Seidman JG, Seidman CE. Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy. Science 2015;349:982–986.
-
(2015)
Science
, vol.349
, pp. 982-986
-
-
Hinson, J.T.1
Chopra, A.2
Nafissi, N.3
Polacheck, W.J.4
Benson, C.C.5
Swist, S.6
Gorham, J.7
Yang, L.8
Schafer, S.9
Sheng, C.C.10
Haghighi, A.11
Homsy, J.12
Hubner, N.13
Church, G.14
Cook, S.A.15
Linke, W.A.16
Chen, C.S.17
Seidman, J.G.18
Seidman, C.E.19
-
30
-
-
84964575491
-
European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology
-
Elliott P, Charron P, Blanes JRG, Tavazzi L, Tendera M, Konté M, Laroche C, Maggioni AP. European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology. Eur Heart J 2015;37:164–173.
-
(2015)
Eur Heart J
, vol.37
, pp. 164-173
-
-
Elliott, P.1
Charron, P.2
Blanes, J.R.G.3
Tavazzi, L.4
Tendera, M.5
Konté, M.6
Laroche, C.7
Maggioni, A.P.8
-
31
-
-
0347363881
-
Exact log-rank tests for unequal follow-up
-
Heinze G, Gnant M, Schemper M. Exact log-rank tests for unequal follow-up. Biometrics 2003;59:1151–1157.
-
(2003)
Biometrics
, vol.59
, pp. 1151-1157
-
-
Heinze, G.1
Gnant, M.2
Schemper, M.3
|