-
1
-
-
70449192269
-
Asymmetrical hypertrophy of the heart in young adults
-
Teare D. Asymmetrical hypertrophy of the heart in young adults. Br. Heart J. 20(1), 1-8 (1958).
-
(1958)
Br. Heart J.
, vol.20
, Issue.1
, pp. 1-8
-
-
Teare, D.1
-
2
-
-
0029083650
-
Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults
-
Maron BJ, Gardin JM, Flack JM et al. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation 92(4), 785-789 (1995).
-
(1995)
Circulation
, vol.92
, Issue.4
, pp. 785-789
-
-
Maron, B.J.1
Gardin, J.M.2
Flack, J.M.3
-
3
-
-
0031052480
-
The management of hypertrophic cardiomyopathy
-
Spirito P, Seidman CE, McKenna WJ, Maron BJ. The management of hypertrophic cardiomyopathy. N. Engl. J Med. 336(11), 775-785 (1997).
-
(1997)
N. Engl. J. Med.
, vol.336
, Issue.11
, pp. 775-785
-
-
Spirito, P.1
Seidman, C.E.2
McKenna, W.J.3
Maron, B.J.4
-
4
-
-
0037454158
-
Hypertrophic cardiomyopathy in a large community-based population: Clinical outcome and identification of risk factors for sudden cardiac death and clinical deterioration
-
Kofflard MJ, Ten Cate FJ, van der Lee C, van Domburg RT. Hypertrophic cardiomyopathy in a large community-based population: clinical outcome and identification of risk factors for sudden cardiac death and clinical deterioration. J. Am. Coll. Cardiol. 41(6), 987-993 (2003).
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, Issue.6
, pp. 987-993
-
-
Kofflard, M.J.1
Ten Cate, F.J.2
van der Lee, C.3
van Domburg, R.T.4
-
5
-
-
29144506700
-
Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia
-
Wolf CM, Moskowitz IP, Arno S et al. Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia. Proc. Natl Acad. Sci. USA 102(50), 18123-18128 (2005).
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, Issue.50
, pp. 18123-18128
-
-
Wolf, C.M.1
Moskowitz, I.P.2
Arno, S.3
-
6
-
-
1942436120
-
Long-term follow-up of implantable cardioverter defibrillator therapy for hypertrophic cardiomyopathy
-
Jayatilleke I, Dootan A, Ingles J et al. Long-term follow-up of implantable cardioverter defibrillator therapy for hypertrophic cardiomyopathy. Am. J. Cardiol. 93(9), 1192-1194 (2004).
-
(2004)
Am. J. Cardiol.
, vol.93
, Issue.9
, pp. 1192-1194
-
-
Jayatilleke, I.1
Dootan, A.2
Ingles, J.3
-
7
-
-
22144443150
-
Current concepts of the pathogenesis and treatment of hypertrophic cardiomyopathy
-
Roberts R, Sigwart U. Current concepts of the pathogenesis and treatment of hypertrophic cardiomyopathy. Circulation 112(2), 293-296 (2005).
-
(2005)
Circulation
, vol.112
, Issue.2
, pp. 293-296
-
-
Roberts, R.1
Sigwart, U.2
-
8
-
-
0024426784
-
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1
-
Jarcho JA, McKenna W, Pare JA et al. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N. Engl. J. Med. 321(20), 1372-1378 (1989).
-
(1989)
N. Engl. J. Med.
, vol.321
, Issue.20
, pp. 1372-1378
-
-
Jarcho, J.A.1
McKenna, W.2
Pare, J.A.3
-
9
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance AA, Kass S, Tanigawa G et al. A molecular basis for familial hypertrophic cardiomyopathy: a β cardiac myosin heavy chain gene missense mutation. Cell 62(5), 999-1006 (1990).
-
(1990)
Cell
, vol.62
, Issue.5
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
-
10
-
-
0025104401
-
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease
-
Solomon SD, Jarcho JA, McKenna W et al. Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease. J. Clin. Invest. 86(3), 993-999 (1990).
-
(1990)
J. Clin. Invest.
, vol.86
, Issue.3
, pp. 993-999
-
-
Solomon, S.D.1
Jarcho, J.A.2
McKenna, W.3
-
11
-
-
0027420155
-
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
-
Watkins H, MacRae C, Thierfelder L et al. A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nat. Genet. 3(4), 333-337 (1993).
-
(1993)
Nat. Genet.
, vol.3
, Issue.4
, pp. 333-337
-
-
Watkins, H.1
MacRae, C.2
Thierfelder, L.3
-
12
-
-
0027180678
-
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2
-
Thierfelder L, MacRae C, Watkins H et al. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proc. Natl Acad. Sci. USA 90(13), 6270-6274 (1993).
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, Issue.13
, pp. 6270-6274
-
-
Thierfelder, L.1
MacRae, C.2
Watkins, H.3
-
13
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins H, Conner D, Thierfelder L et al. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat. Genet. 11(4), 434-437 (1995).
-
(1995)
Nat. Genet.
, vol.11
, Issue.4
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
-
14
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
-
Poetter K, Jiang H, Hassanzadeh S et al. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat. Genet. 13(1), 63-69 (1996).
-
(1996)
Nat. Genet.
, vol.13
, Issue.1
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.2
Hassanzadeh, S.3
-
15
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura A, Harada H, Park JE et al. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat. Genet. 16(4), 379-382 (1997).
-
(1997)
Nat. Genet.
, vol.16
, Issue.4
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.E.3
-
16
-
-
0035378612
-
First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy
-
Hoffmann B, Schmidt-Traub H, Perrot A, Osterziel KJ, Gessner R. First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy. Hum. Mutat. 17(6), 524 (2001).
-
(2001)
Hum. Mutat.
, vol.17
, Issue.6
, pp. 524
-
-
Hoffmann, B.1
Schmidt-Traub, H.2
Perrot, A.3
Osterziel, K.J.4
Gessner, R.5
-
17
-
-
9644281144
-
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy
-
Hayashi T, Arimura T, Itoh-Satoh M et al. Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy. J. Am. Coll. Cardiol. 44(11), 2192-2201 (2004).
-
(2004)
J. Am. Coll. Cardiol.
, vol.44
, Issue.11
, pp. 2192-2201
-
-
Hayashi, T.1
Arimura, T.2
Itoh-Satoh, M.3
-
18
-
-
0037453074
-
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy
-
Geier C, Perrot A, Ozcelik C et al. Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy. Circulation 107(10), 1390-1395 (2003).
-
(2003)
Circulation
, vol.107
, Issue.10
, pp. 1390-1395
-
-
Geier, C.1
Perrot, A.2
Ozcelik, C.3
-
19
-
-
0033610050
-
Structural analysis of the titin gene in hypertrophic cardiomyopathy: Identification of a novel disease gene
-
Satoh M, Takahashi M, Sakamoto T et al. Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene. Biochem. Blophys. Res. Commun. 262(2), 411-417 (1999).
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.262
, Issue.2
, pp. 411-417
-
-
Satoh, M.1
Takahashi, M.2
Sakamoto, T.3
-
20
-
-
0027954269
-
Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy
-
Anan R, Greve G, Thierfelder L et al. Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy. J. Clin. Invest. 93(1), 280-285 (1994).
-
(1994)
J. Clin. Invest.
, vol.93
, Issue.1
, pp. 280-285
-
-
Anan, R.1
Greve, G.2
Thierfelder, L.3
-
21
-
-
0029029027
-
Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: A modulator of cardiac contraction?
-
Gautel M, Zuffardi O, Freiburg A, Labeit S. Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction? EMBO J. 14(9), 1952-1960 (1995).
-
(1995)
EMBO J.
, vol.14
, Issue.9
, pp. 1952-1960
-
-
Gautel, M.1
Zuffardi, O.2
Freiburg, A.3
Labeit, S.4
-
22
-
-
11144297937
-
Biology of the troponin complex in cardiac myocytes
-
Parmacek MS, Solaro RJ. Biology of the troponin complex in cardiac myocytes. Prog. Cardiovasc. Dis. 47(3), 159-176 (2004).
-
(2004)
Prog. Cardiovasc. Dis.
, vol.47
, Issue.3
, pp. 159-176
-
-
Parmacek, M.S.1
Solaro, R.J.2
-
24
-
-
20844448376
-
Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: Clinical, genetic and functional consequences
-
Doolan A, Tebo M, Ingles J et al. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences. J. Mol. Cell. Cardiol. 38(2), 387-393 (2005).
-
(2005)
J. Mol. Cell. Cardiol.
, vol.38
, Issue.2
, pp. 387-393
-
-
Doolan, A.1
Tebo, M.2
Ingles, J.3
-
25
-
-
0034622609
-
Clinical features of hypertrophic: Cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene
-
Kokado H, Shimizu M, Yoshio H et al. Clinical features of hypertrophic: cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene. Circulation 102(6), 663-669 (2000).
-
(2000)
Circulation
, vol.102
, Issue.6
, pp. 663-669
-
-
Kokado, H.1
Shimizu, M.2
Yoshio, H.3
-
26
-
-
0038701678
-
Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy
-
Crilley JG, Boehm EA, Blair E et al. Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy. J. Am. Coll. Cardiol. 41(10), 1776-1782 (2003).
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, Issue.10
, pp. 1776-1782
-
-
Crilley, J.G.1
Boehm, E.A.2
Blair, E.3
-
27
-
-
0035822608
-
Reduced myocardial sarcoplasmic reticulum Ca(2+)-ATPase mRNA expression and biphasic force-frequency relations in patients with hypertrophic cardiomyopathy
-
Somura F, Izawa H, Iwase M et al. Reduced myocardial sarcoplasmic reticulum Ca(2+)-ATPase mRNA expression and biphasic force-frequency relations in patients with hypertrophic cardiomyopathy. Circulation 104(6), 658-663 (2001).
-
(2001)
Circulation
, vol.104
, Issue.6
, pp. 658-663
-
-
Somura, F.1
Izawa, H.2
Iwase, M.3
-
28
-
-
9044230117
-
Endothelin-1 and its receptor in hypertrophic cardiomyopathy
-
Hasegawa K, Fujiwara H, Koshiji M et al. Endothelin-1 and its receptor in hypertrophic cardiomyopathy. Hypertension 27(2), 259-264 (1996).
-
(1996)
Hypertension
, vol.27
, Issue.2
, pp. 259-264
-
-
Hasegawa, K.1
Fujiwara, H.2
Koshiji, M.3
-
29
-
-
0030877545
-
Overexpression of transforming growth factor-β1 and insulin-like growth factor-I in patients with idiopathic hypertrophic cardiomyopathy
-
Li RK, Li G, Mickle DA et al. Overexpression of transforming growth factor-β1 and insulin-like growth factor-I in patients with idiopathic hypertrophic cardiomyopathy. Circulation 96(3), 874-881 (1997).
-
(1997)
Circulation
, vol.96
, Issue.3
, pp. 874-881
-
-
Li, R.K.1
Li, G.2
Mickle, D.A.3
-
30
-
-
10744220034
-
Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy
-
Hayashi T, Arimura T, Ueda K et al. Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy. Biochem. Biophys. Res. Commun. 313(1), 178-184 (2004).
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.313
, Issue.1
, pp. 178-184
-
-
Hayashi, T.1
Arimura, T.2
Ueda, K.3
-
31
-
-
31944450889
-
A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy
-
Haghighi K, Kolokathis F, Gramolini AO et al. A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy. Proc. Natl Acad. Sci. USA 103(5), 1388-1393 (2006).
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, Issue.5
, pp. 1388-1393
-
-
Haghighi, K.1
Kolokathis, F.2
Gramolini, A.O.3
-
32
-
-
85047687537
-
Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human
-
Haghighi K, Kolokathis F, Pater L et al. Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human. J. Clin. Invest. 111(6), 869-876 (2003).
-
(2003)
J. Clin. Invest.
, vol.111
, Issue.6
, pp. 869-876
-
-
Haghighi, K.1
Kolokathis, F.2
Pater, L.3
-
33
-
-
0037470512
-
Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban
-
Schmitt JP, Kamisago M, Asahi M et al. Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban. Science 299(5611), 1410-1413 (2003).
-
(2003)
Science
, vol.299
, Issue.5611
, pp. 1410-1413
-
-
Schmitt, J.P.1
Kamisago, M.2
Asahi, M.3
-
34
-
-
0344406208
-
Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy
-
Minamisawa S, Sato Y, Tatsuguchi Y et al. Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy. Biochem. Biophys. Res. Commun. 304(1), 1-4 (2003).
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.304
, Issue.1
, pp. 1-4
-
-
Minamisawa, S.1
Sato, Y.2
Tatsuguchi, Y.3
-
35
-
-
0035859215
-
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
-
Gollob MH, Green MS, Tang AS et al. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N. Engl. J. Med. 344(24), 1823-1831 (2001).
-
(2001)
N. Engl. J. Med.
, vol.344
, Issue.24
, pp. 1823-1831
-
-
Gollob, M.H.1
Green, M.S.2
Tang, A.S.3
-
36
-
-
19944434362
-
Glycogen storage diseases presenting as hypertrophic cardiomyopathy
-
Arad M, Maron BJ, Gorham JM et al. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N. Engl. J. Med. 352(4), 362-372 (2005).
-
(2005)
N. Engl. J. Med.
, vol.352
, Issue.4
, pp. 362-372
-
-
Arad, M.1
Maron, B.J.2
Gorham, J.M.3
-
37
-
-
0035872209
-
Mutations in the γ(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: Evidence for the central role of energy compromise in disease pathogenesis
-
Blair E, Redwood C. Ashrafian H et al. Mutations in the γ(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Hum. Mol. Genet. 10(11), 1215-1220 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, Issue.11
, pp. 1215-1220
-
-
Blair, E.1
Redwood, C.2
Ashrafian, H.3
-
38
-
-
4544344055
-
Prevalence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathy
-
Chimenti C, Pieroni M, Morgante E et al. Prevalence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathy. Circulation 110(9), 1047-1053 (2004).
-
(2004)
Circulation
, vol.110
, Issue.9
, pp. 1047-1053
-
-
Chimenti, C.1
Pieroni, M.2
Morgante, E.3
-
39
-
-
24944575163
-
Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children
-
Yang Z, McMahon CJ, Smith LR et al. Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children. Circulation 112(11), 1612-1617 (2005).
-
(2005)
Circulation
, vol.112
, Issue.11
, pp. 1612-1617
-
-
Yang, Z.1
McMahon, C.J.2
Smith, L.R.3
-
40
-
-
20044396901
-
Natural history and familial characteristics of isolated left ventricular non-compaction
-
Murphy RT, Thaman R, Blanes JG et al. Natural history and familial characteristics of isolated left ventricular non-compaction. Eur. Heart J. 26(2), 187-192 (2005).
-
(2005)
Eur. Heart J.
, vol.26
, Issue.2
, pp. 187-192
-
-
Murphy, R.T.1
Thaman, R.2
Blanes, J.G.3
-
41
-
-
0025106446
-
Isolated noncompaction of left ventricular myocardium. A study of eight cases
-
Chin TK, Perloff JK, Williams RG, Jue K, Mohrmann R. Isolated noncompaction of left ventricular myocardium. A study of eight cases. Circulation 82 (2), 507-513 (1990).
-
(1990)
Circulation
, vol.82
, Issue.2
, pp. 507-513
-
-
Chin, T.K.1
Perloff, J.K.2
Williams, R.G.3
Jue, K.4
Mohrmann, R.5
-
42
-
-
20044382630
-
Yield of genetic testing in hypertrophic cardiomyopathy
-
Van Driest SL, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Yield of genetic testing in hypertrophic cardiomyopathy. Mayo Clin. Proc. 80(6), 739-744 (2005).
-
(2005)
Mayo Clin. Proc.
, vol.80
, Issue.6
, pp. 739-744
-
-
Van Driest, S.L.1
Ommen, S.R.2
Tajik, A.J.3
Gersh, B.J.4
Ackerman, M.J.5
-
43
-
-
0037630018
-
Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
Richard P, Charron P, Carrier L et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 107(17), 2227-2232 (2003).
-
(2003)
Circulation
, vol.107
, Issue.17
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
-
44
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
Van Driest SL, Vasile VC, Ommen SR et al. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 44(9), 1903-1910 (2004).
-
(2004)
J. Am. Coll. Cardiol.
, vol.44
, Issue.9
, pp. 1903-1910
-
-
Van Driest, S.L.1
Vasile, V.C.2
Ommen, S.R.3
-
45
-
-
33646757738
-
Compound and double mutations in patients with hypertrophic cardiomyopathy: Implications for genetic testing and counselling
-
Ingles J, Doolan A, Chiu C et al. Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling. J. Med. Genet. 42(10), E59 (2005).
-
(2005)
J. Med. Genet.
, vol.42
, Issue.10
-
-
Ingles, J.1
Doolan, A.2
Chiu, C.3
-
46
-
-
0036117921
-
The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model
-
Semsarian C, Ahmad I, Giewat M et al. The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model. J. Clin. Invest. 109(8), 1013-1020 (2002).
-
(2002)
J. Clin. Invest.
, vol.109
, Issue.8
, pp. 1013-1020
-
-
Semsarian, C.1
Ahmad, I.2
Giewat, M.3
-
47
-
-
0035253502
-
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricutar cardiomyopathy type 2 (ARVD2)
-
Tiso N, Stephan DA, Nava A et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricutar cardiomyopathy type 2 (ARVD2). Hum. Mol. Genet. 10(3), 189-194 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, Issue.3
, pp. 189-194
-
-
Tiso, N.1
Stephan, D.A.2
Nava, A.3
-
48
-
-
0035895322
-
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
-
Priori SG, Napolitano C, Tiso N et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 103(2), 196-200 (2001).
-
(2001)
Circulation
, vol.103
, Issue.2
, pp. 196-200
-
-
Priori, S.G.1
Napolitano, C.2
Tiso, N.3
-
49
-
-
0035205336
-
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
-
Lahat H, Pras E, Olender T et al. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am. J. Hum. Genet. 69(6), 1378-1384 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.69
, Issue.6
, pp. 1378-1384
-
-
Lahat, H.1
Pras, E.2
Olender, T.3
-
50
-
-
0035201270
-
A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy
-
Semsarian C, Healey MJ, Fatkin D et al. A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 33(11), 2055-2060 (2001).
-
(2001)
J. Mol. Cell. Cardiol.
, vol.33
, Issue.11
, pp. 2055-2060
-
-
Semsarian, C.1
Healey, M.J.2
Fatkin, D.3
-
51
-
-
3242748308
-
Progression of left ventricular hypertrophy and the angiotensin-converting enzyme gene polymorphism in hypertrophic cardiomyopathy
-
Doolan G, Nguyen L, Chung J, Ingles J, Semsarian C. Progression of left ventricular hypertrophy and the angiotensin-converting enzyme gene polymorphism in hypertrophic cardiomyopathy. Int. J. Cardiol. 96(2), 157-163 (2004).
-
(2004)
Int. J. Cardiol.
, vol.96
, Issue.2
, pp. 157-163
-
-
Doolan, G.1
Nguyen, L.2
Chung, J.3
Ingles, J.4
Semsarian, C.5
-
52
-
-
0031597427
-
AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy
-
Osterop AP, Kofflard MJ, Sandkuijl LA et al. AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy. Hypertension 32(5), 825-830 (1998).
-
(1998)
Hypertension
, vol.32
, Issue.5
, pp. 825-830
-
-
Osterop, A.P.1
Kofflard, M.J.2
Sandkuijl, L.A.3
-
53
-
-
0035672057
-
Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy
-
Deinum J, van Gool JM, Kofflard MJ, ten Cate FJ, Danser AH, Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy. Hypertension 38(6), 1278-1281 (2001).
-
(2001)
Hypertension
, vol.38
, Issue.6
, pp. 1278-1281
-
-
Deinum, J.1
van Gool, J.M.2
Kofflard, M.J.3
ten Cate, F.J.4
Danser, A.H.5
-
54
-
-
0034502439
-
Variants of trophic factors and expression of cardiac hypertrophy in patients with hypertrophic cardiomyopathy
-
Patel R, Lim DS, Reddy D et al. Variants of trophic factors and expression of cardiac hypertrophy in patients with hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 32(12), 2369-2377 (2000).
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, Issue.12
, pp. 2369-2377
-
-
Patel, R.1
Lim, D.S.2
Reddy, D.3
-
55
-
-
0034628532
-
Efficacy of implantable cardioverter-defibrillators for the prevention of sudden death in patients with hypertrophic cardiomyopathy
-
Maron BJ, Shen WK, Link MS et al. Efficacy of implantable cardioverter-defibrillators for the prevention of sudden death in patients with hypertrophic cardiomyopathy. N. Engl. J. Med. 342(6). 365-373 (2000).
-
(2000)
N. Engl. J. Med.
, vol.342
, Issue.6
, pp. 365-373
-
-
Maron, B.J.1
Shen, W.K.2
Link, M.S.3
-
56
-
-
0035852766
-
Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy
-
Lim DS, Lutucuta S, Bachireddy P et al. Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy. Circulation 103(6), 789-791 (2001).
-
(2001)
Circulation
, vol.103
, Issue.6
, pp. 789-791
-
-
Lim, D.S.1
Lutucuta, S.2
Bachireddy, P.3
-
57
-
-
23344440434
-
Prevention of cardiac hypertrophy by atorvastatin in a transgenic rabbit model of human hypertrophic cardiomyopathy
-
Senthil V, Chen SN, Tsybouleva N et al. Prevention of cardiac hypertrophy by atorvastatin in a transgenic rabbit model of human hypertrophic cardiomyopathy. Circ. Res. 97(3), 285-292 (2005).
-
(2005)
Circ. Res.
, vol.97
, Issue.3
, pp. 285-292
-
-
Senthil, V.1
Chen, S.N.2
Tsybouleva, N.3
-
58
-
-
12144288228
-
Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy
-
Tsybouleva N, Zhang L, Chen S et al. Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy. Circulation 109(10), 1284-1291 (2004).
-
(2004)
Circulation
, vol.109
, Issue.10
, pp. 1284-1291
-
-
Tsybouleva, N.1
Zhang, L.2
Chen, S.3
-
59
-
-
0037058868
-
Prevalence and severity of 'benign' mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy
-
Van Driest SL, Ackerman MJ, Ommen SR et al. Prevalence and severity of 'benign' mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy. Circulation 106(24), 3085-3090 (2002).
-
(2002)
Circulation
, vol.106
, Issue.24
, pp. 3085-3090
-
-
Van Driest, S.L.1
Ackerman, M.J.2
Ommen, S.R.3
-
60
-
-
0041663609
-
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
-
Van Driest SL, Ellsworth EG, Ommen SR et al. Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. Circulation 108(4), 445-451 (2003).
-
(2003)
Circulation
, vol.108
, Issue.4
, pp. 445-451
-
-
Van Driest, S.L.1
Ellsworth, E.G.2
Ommen, S.R.3
-
61
-
-
4043081356
-
Comprehensive analyst of the β-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy
-
Van Driest SL, Jaeger MA, Ommen SR et al. Comprehensive analyst of the β-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 44(3), 602-610 (2004).
-
(2004)
J. Am. Coll. Cardiol.
, vol.44
, Issue.3
, pp. 602-610
-
-
Van Driest, S.L.1
Jaeger, M.A.2
Ommen, S.R.3
-
62
-
-
0037134832
-
Prevalence and age-dependence of malignant mutations in the P-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: A comprehensive outpatient perspective
-
Ackerman MJ, VanDriest SL, Ommen SR et al. Prevalence and age-dependence of malignant mutations in the P-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective. J. Am. Coll. Cardiol. 39(12), 2042-2048 (2002).
-
(2002)
J. Am. Coll. Cardiol.
, vol.39
, Issue.12
, pp. 2042-2048
-
-
Ackerman, M.J.1
VanDriest, S.L.2
Ommen, S.R.3
-
63
-
-
12444270692
-
Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy
-
Erdmann J, Daehmlow S, Wischke S et al. Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy. Clin. Genet. 64(4), 339-349 (2003).
-
(2003)
Clin. Genet.
, vol.64
, Issue.4
, pp. 339-349
-
-
Erdmann, J.1
Daehmlow, S.2
Wischke, S.3
-
64
-
-
0038125906
-
Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden
-
Morner S, Richard P, Kazzam E et al. Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden. J. Mol. Cell. Cardiol. 35(7), 841-849 (2003).
-
(2003)
J. Mol. Cell. Cardiol.
, vol.35
, Issue.7
, pp. 841-849
-
-
Morner, S.1
Richard, P.2
Kazzam, E.3
-
65
-
-
0344878860
-
The cardiac β-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population
-
Jaaskelainen P, Soranta M, Miettinen R et al. The cardiac β-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population. J. Am. Coll. Cardiol. 32(6), 1709-1716 (1998).
-
(1998)
J. Am. Coll. Cardiol.
, vol.32
, Issue.6
, pp. 1709-1716
-
-
Jaaskelainen, P.1
Soranta, M.2
Miettinen, R.3
-
66
-
-
0344146553
-
The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland
-
Jaaskelainen P, Miettinen R, Silvennoinen K et al. The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland. J. Mol. Cell. Cardiol. 31(11), 2031-2036 (1999).
-
(1999)
J. Mol. Cell. Cardiol.
, vol.31
, Issue.11
, pp. 2031-2036
-
-
Jaaskelainen, P.1
Miettinen, R.2
Silvennoinen, K.3
-
67
-
-
0036019515
-
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland
-
Jaaskelainen P, Kuusisto J, Miettinen R et al. Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland. J. Mol. Med. 80(7), 412-422 (2002).
-
(2002)
J. Mol. Med.
, vol.80
, Issue.7
, pp. 412-422
-
-
Jaaskelainen, P.1
Kuusisto, J.2
Miettinen, R.3
-
68
-
-
0036593250
-
No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy
-
Karkkainen S, Peuhkurinen K, Jaaskelainen P et al. No variants in the cardiac actin gene in Finnish patients with dilated or hypertrophic cardiomyopathy. Am. Heart J. 143(6), E6 (2002).
-
(2002)
Am. Heart J.
, vol.143
, Issue.6
-
-
Karkkainen, S.1
Peuhkurinen, K.2
Jaaskelainen, P.3
-
69
-
-
0041866796
-
Hypertrophic cardiomyopathy: Low frequency of mutations in the β-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients
-
Garcia-Castro M, Reguero JR, Batalla A et al. Hypertrophic cardiomyopathy: low frequency of mutations in the β-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients. Clin. Chem. 49(8), 1279-1285 (2003).
-
(2003)
Clin. Chem.
, vol.49
, Issue.8
, pp. 1279-1285
-
-
Garcia-Castro, M.1
Reguero, J.R.2
Batalla, A.3
-
70
-
-
0035936792
-
The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms
-
Seidman JG, Seidman CE. The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell 104(4), 557-567 (2001).
-
(2001)
Cell
, vol.104
, Issue.4
, pp. 557-567
-
-
Seidman, J.G.1
Seidman, C.E.2
|