-
1
-
-
0037630018
-
Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 2003;107:2227-2232.
-
(2003)
Circulation
, vol.107
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
Ledeuil, C.4
Cheav, T.5
Pichereau, C.6
Benaiche, A.7
Isnard, R.8
Dubourg, O.9
Burban, M.10
Gueffet, J.P.11
Millaire, A.12
Desnos, M.13
Schwartz, K.14
Hainque, B.15
Komajda, M.16
-
2
-
-
16344385637
-
Sarcomeric genotyping in hypertrophic cardiomyopathy
-
Van Driest S, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Sarcomeric genotyping in hypertrophic cardiomyopathy. Mayo Clin Proc 2005;80:463-469.
-
(2005)
Mayo Clin Proc
, vol.80
, pp. 463-469
-
-
Van Driest, S.1
Ommen, S.R.2
Tajik, A.J.3
Gersh, B.J.4
Ackerman, M.J.5
-
3
-
-
0032499634
-
Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene
-
Charron P, Dubourg O, Desnos M, Bennaceur M, Carrier L, Camproux AC, Isnard R, Hagege A, Langlard JM, Bonne G, Richard P, Hainque B, Bouhour JB, Schwartz K, Komajda M. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene. Circulation 1998;97:2230-2236.
-
(1998)
Circulation
, vol.97
, pp. 2230-2236
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Bennaceur, M.4
Carrier, L.5
Camproux, A.C.6
Isnard, R.7
Hagege, A.8
Langlard, J.M.9
Bonne, G.10
Richard, P.11
Hainque, B.12
Bouhour, J.B.13
Schwartz, K.14
Komajda, M.15
-
4
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
Van Driest SL, Vasile VC, Ommen SR, Will ML, Tajik AJ, Gersh BJ, Ackerman MJ. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol 2004;44:1903-1910.
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 1903-1910
-
-
Van Driest, S.L.1
Vasile, V.C.2
Ommen, S.R.3
Will, M.L.4
Tajik, A.J.5
Gersh, B.J.6
Ackerman, M.J.7
-
5
-
-
0034907103
-
Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy
-
Erdmann J, Raible J, Maki-Abadi J, Hummel M, Hammann J, Wollnik B, Frantz E, Fleck E, Hetzer R, Regitz-Zagrosek V. Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy. J Am Coll Cardiol 2001;38:322-330.
-
(2001)
J Am Coll Cardiol
, vol.38
, pp. 322-330
-
-
Erdmann, J.1
Raible, J.2
Maki-Abadi, J.3
Hummel, M.4
Hammann, J.5
Wollnik, B.6
Frantz, E.7
Fleck, E.8
Hetzer, R.9
Regitz-Zagrosek, V.10
-
6
-
-
56649116133
-
Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene
-
Ehlermann P, Weichenhan D, Zehelein J, Steen H, Pribe R, Zeller R, Lehrke S, Zugck C, Ivandic BT, Katus HA. Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene. BMC Med Genet 2008;9:95.
-
(2008)
BMC Med Genet
, vol.9
, pp. 95
-
-
Ehlermann, P.1
Weichenhan, D.2
Zehelein, J.3
Steen, H.4
Pribe, R.5
Zeller, R.6
Lehrke, S.7
Zugck, C.8
Ivandic, B.T.9
Katus, H.A.10
-
7
-
-
0036019515
-
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland
-
Jaaskelainen P, Kauusisto J, Miettinen R, Karkkainen P, Karkkainen S, Heikkinen S, Peltola P, Pihlajamaki J, Vauhkonen I, Laakso M. Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland. J Mol Med 2002;80:412-422.
-
(2002)
J Mol Med
, vol.80
, pp. 412-422
-
-
Jaaskelainen, P.1
Kauusisto, J.2
Miettinen, R.3
Karkkainen, P.4
Karkkainen, S.5
Heikkinen, S.6
Peltola, P.7
Pihlajamaki, J.8
Vauhkonen, I.9
Laakso, M.10
-
8
-
-
34848876400
-
Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy
-
Daw EW, Chen SN, Czernuszewicz G, Lombardi R, Lu Y, Ma J, Roberts R, Shete S, Marian AJ. Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy. Hum Mol Genet 2007; 16:2463-2471.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2463-2471
-
-
Daw, E.W.1
Chen, S.N.2
Czernuszewicz, G.3
Lombardi, R.4
Lu, Y.5
Ma, J.6
Roberts, R.7
Shete, S.8
Marian, A.J.9
-
9
-
-
50649111374
-
Large scale analysis of HCM mutations in sudden cardiac death
-
Brion M, Allegue C, Monserrat L. Hermida M, Castro- Beiras A, Carracedo A. Large scale analysis of HCM mutations in sudden cardiac death. Forensic Sci Int (Genetics Supplement Series) 2008;1:549-550.
-
(2008)
Forensic Sci Int (Genetics Supplement Series)
, vol.1
, pp. 549-550
-
-
Brion, M.1
Allegue, C.2
Monserrat, L.3
Hermida, M.4
Castro- Beiras, A.5
Carracedo, A.6
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