-
1
-
-
0023130164
-
Hypertrophic cardiomyopathy: Interrelations of clinical manifestations, pathophysiology, and therapy
-
Maron BJ, Bonow RO, Cannon RO, Leon MB, Epstein SE. Hypertrophic cardiomyopathy: interrelations of clinical manifestations, pathophysiology. and therapy. N Engl J Med. 1987;316:780-789, 844-852.
-
(1987)
N Engl J Med
, vol.316
, pp. 780-789
-
-
Maron, B.J.1
Bonow, R.O.2
Cannon, R.O.3
Leon, M.B.4
Epstein, S.E.5
-
2
-
-
0029118518
-
Hypertrophic cardiomyopathy: Clinical spectrum and treatment
-
Wigle ED, Rakowski H, Kimball BP, Williams WG, Hypertrophic cardiomyopathy: clinical spectrum and treatment. Circulation. 1995;92:1680-1692.
-
(1995)
Circulation
, vol.92
, pp. 1680-1692
-
-
Wigle, E.D.1
Rakowski, H.2
Kimball, B.P.3
Williams, W.G.4
-
3
-
-
0031052480
-
The management of hypertrophic cardiomyopathy
-
Spirito P, Seidman CE, McKenna WJ, Maron BJ, The management of hypertrophic cardiomyopathy. N Engl J Med. 1997;336:775-785.
-
(1997)
N Engl J Med
, vol.336
, pp. 775-785
-
-
Spirito, P.1
Seidman, C.E.2
McKenna, W.J.3
Maron, B.J.4
-
4
-
-
0025676652
-
Abnormal blood pressure response during exercise in hypertrophic cardiomyopathy
-
Frenneaux MP, Counihan PJ, Caforio ALP, Chikamori T, MacKenna WJ. Abnormal blood pressure response during exercise in hypertrophic cardiomyopathy. Circulation. 1990;82:1995-2002.
-
(1990)
Circulation
, vol.82
, pp. 1995-2002
-
-
Frenneaux, M.P.1
Counihan, P.J.2
Caforio, A.L.P.3
Chikamori, T.4
MacKenna, W.J.5
-
5
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A β-cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance AAT, Kass S, Tanigawa G, Vosberg H-P, McKenna W, Seidman CE, Seidman JG. A molecular basis for familial hypertrophic cardiomyopathy: a β-cardiac myosin heavy chain gene missense mutation. Cell. 1990;62:999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.T.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.-P.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
6
-
-
0028178083
-
α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman C. α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell. 1994;77:701-712.
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
Lamas, R.4
McKenna, W.5
Vosberg, H.P.6
Seidman, J.G.7
Seidman, C.8
-
7
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, Labeit S, James M, Weissenbach J, Vosberg HP, Fiszman M, Komajda M, Schwanz K. Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat Genet. 1995;11:438-440.
-
(1995)
Nat Genet
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
Cruaud, C.4
Richard, P.5
Hainque, B.6
Gautel, M.7
Labeit, S.8
James, M.9
Weissenbach, J.10
Vosberg, H.P.11
Fiszman, M.12
Komajda, M.13
Schwanz, K.14
-
8
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna W, Maron BJ, Seidman JG, Seidman CE. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat Genet. 1995;11:434-437.
-
(1995)
Nat Genet
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
MacRae, C.5
McKenna, W.6
Maron, B.J.7
Seidman, J.G.8
Seidman, C.E.9
-
9
-
-
15844400653
-
Mutations in either of the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
-
Poetter K, Jiang HE, Hassenzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, Sellers JR, Fananapazir L, Epstein ND. Mutations in either of the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat Genet. 1996;13:63-69.
-
(1996)
Nat Genet
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.E.2
Hassenzadeh, S.3
Master, S.R.4
Chang, A.5
Dalakas, M.C.6
Rayment, I.7
Sellers, J.R.8
Fananapazir, L.9
Epstein, N.D.10
-
10
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura A, Harada H, Park J-E, Nishi H, Satoh M, Takahashi M, Hiroi S, Sasaoka T, Ohbuchi N, Nakamura T, Koyanagi T, Hwang T-H, Choo J-A, Chung K-S, Hasegawa A, Nagai R, Qkazaki O, Nakamura H, Matsuzaki M, Sakamoto T, Toshima H, Koga Y, Imaizumi T, Sasazuki T. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat Genet. 1997;19:379-382.
-
(1997)
Nat Genet
, vol.19
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.-E.3
Nishi, H.4
Satoh, M.5
Takahashi, M.6
Hiroi, S.7
Sasaoka, T.8
Ohbuchi, N.9
Nakamura, T.10
Koyanagi, T.11
Hwang, T.-H.12
Choo, J.-A.13
Chung, K.-S.14
Hasegawa, A.15
Nagai, R.16
Qkazaki, O.17
Nakamura, H.18
Matsuzaki, M.19
Sakamoto, T.20
Toshima, H.21
Koga, Y.22
Imaizumi, T.23
Sasazuki, T.24
more..
-
11
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins HG, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Engl J Med. 1992;326:1108-1114.
-
(1992)
N Engl J Med
, vol.326
, pp. 1108-1114
-
-
Watkins, H.G.1
Rosenzweig, A.2
Hwang, D.S.3
Levi, T.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
13
-
-
0029166817
-
Recent advances in the molecular genetics of hypertrophic cardiomyopathy
-
Marian AJ, Roberts R. Recent advances in the molecular genetics of hypertrophic cardiomyopathy. Circulation. 1995;92:1336-1347.
-
(1995)
Circulation
, vol.92
, pp. 1336-1347
-
-
Marian, A.J.1
Roberts, R.2
-
14
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
Watkins H, McKenna W, Thierfelder L, Suk HJ, Anan R, O'Donoghue A, Spirito P, Matsumori A, Moravec CS, Seidman JG, Seidman CE. Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med. 1995;332:1058-1064.
-
(1995)
N Engl J Med
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.2
Thierfelder, L.3
Suk, H.J.4
Anan, R.5
O'Donoghue, A.6
Spirito, P.7
Matsumori, A.8
Moravec, C.S.9
Seidman, J.G.10
Seidman, C.E.11
-
15
-
-
0031052924
-
Sudden death due to troponin T mutations
-
Moolman JC, Corfield VA, Posen B, Ngumbela K, Seidman C, Brink PA, Watkins H. Sudden death due to troponin T mutations. J Am Coll Cardiol. 1997;29:549-555.
-
(1997)
J am Coll Cardiol
, vol.29
, pp. 549-555
-
-
Moolman, J.C.1
Corfield, V.A.2
Posen, B.3
Ngumbela, K.4
Seidman, C.5
Brink, P.A.6
Watkins, H.7
-
16
-
-
0031891357
-
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy associated: A comparison between mutations in the cardiac protein-C and the β-myosin heavy chain genes
-
Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Bonne G, Carrier L, Tesson F, Bouhour J-B, Buzzí J-C, Feíngold J, Schwanz K, Komajda M. Genotype-phenotype correlations in familial hypertrophic cardiomyopathy associated: a comparison between mutations in the cardiac protein-C and the β-myosin heavy chain genes. Ear Heart J. 1998;19:139-145.
-
(1998)
Ear Heart J
, vol.19
, pp. 139-145
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagege, A.5
Bonne, G.6
Carrier, L.7
Tesson, F.8
Bouhour, J.-B.9
Buzzí, J.-C.10
Feíngold, J.11
Schwanz, K.12
Komajda, M.13
-
17
-
-
0031055854
-
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy
-
Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F, Hainque B, Cruaud C, Gary F, Labeit S, Bouhour J-B. Dubourg O, Desnos M, Hagege AA, Trent RJ, Komajda M, Fiszman M, Schwanz K. Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ Res. 1997;80:427-434.
-
(1997)
Circ Res
, vol.80
, pp. 427-434
-
-
Carrier, L.1
Bonne, G.2
Bährend, E.3
Yu, B.4
Richard, P.5
Niel, F.6
Hainque, B.7
Cruaud, C.8
Gary, F.9
Labeit, S.10
Bouhour, J.-B.11
Dubourg, O.12
Desnos, M.13
Hagege, A.A.14
Trent, R.J.15
Komajda, M.16
Fiszman, M.17
Schwanz, K.18
-
18
-
-
0027138216
-
Familial hypertrophic cardiomyopathy: Microsatellite haplotyping and identification of a hot spot for mutations in the β myosin heavy chain gene
-
Dausse E, Komajda M, Fetler L, Dubourg O, Dufour C, Carrier L, Winesnewsky C, Bercovící J, Hengstenberg C, AI-Mahdawi S, Isnard R, Hagege A, Bouhour JB, Desnos M, Beckmann JS, Weissenbach J, Schwanz K, Guicheney P. Familial hypertrophic cardiomyopathy: microsatellite haplotyping and identification of a hot spot for mutations in the β myosin heavy chain gene. J Clin Invest. 1993;92:2807-2813.
-
(1993)
J Clin Invest
, vol.92
, pp. 2807-2813
-
-
Dausse, E.1
Komajda, M.2
Fetler, L.3
Dubourg, O.4
Dufour, C.5
Carrier, L.6
Winesnewsky, C.7
Bercovící, J.8
Hengstenberg, C.9
Ai-Mahdawi, S.10
Isnard, R.11
Hagege, A.12
Bouhour, J.B.13
Desnos, M.14
Beckmann, J.S.15
Weissenbach, J.16
Schwanz, K.17
Guicheney, P.18
-
19
-
-
0028145776
-
Identification of a mutathypertrophicion near a functional site of the β cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy
-
Dufour C, Dausse E, Fetler L, Dubourg O, Bouhour JB, Vosberg H-P, Guicheney P, Komajda M, Schwanz K. Identification of a mutathypertrophicion near a functional site of the β cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy. J Mol Cell Cardiol. 1994;26:1241-1247.
-
(1994)
J Mol Cell Cardiol
, vol.26
, pp. 1241-1247
-
-
Dufour, C.1
Dausse, E.2
Fetler, L.3
Dubourg, O.4
Bouhour, J.B.5
Vosberg, H.-P.6
Guicheney, P.7
Komajda, M.8
Schwanz, K.9
-
20
-
-
0002707964
-
β-Myosin heavy chain gene mutations screening in 18 unrelated families with familial hypertrophic cardiomyopathy
-
Abstract
-
Richard P, Tesson F, Hainque B, Mathieu B, Carrier L, Komajda M, Schwanz K, Guicheney P. β-Myosin heavy chain gene mutations screening in 18 unrelated families with familial hypertrophic cardiomyopathy. J Mol Cell Cardiol. 1996;28:A65. Abstract.
-
(1996)
J Mol Cell Cardiol
, vol.28
-
-
Richard, P.1
Tesson, F.2
Hainque, B.3
Mathieu, B.4
Carrier, L.5
Komajda, M.6
Schwanz, K.7
Guicheney, P.8
-
21
-
-
0028927133
-
Doppler echocardiography in familial hypertrophic cardiomyopathy: The French Cooperative Study
-
Dubourg O, Isnard R, Hagège A, Jondeau G, Desnos M, Sacrez A, Bouhour JB, Messmer Pellenc P, Millaire A, Fetler L, Guicheney P, Schwanz K, Komajda M. Doppler echocardiography in familial hypertrophic cardiomyopathy: the French Cooperative Study. Echocardiography. 1995;12:235-240.
-
(1995)
Echocardiography
, vol.12
, pp. 235-240
-
-
Dubourg, O.1
Isnard, R.2
Hagège, A.3
Jondeau, G.4
Desnos, M.5
Sacrez, A.6
Bouhour, J.B.7
Messmer Pellenc, P.8
Millaire, A.9
Fetler, L.10
Guicheney, P.11
Schwanz, K.12
Komajda, M.13
-
22
-
-
0030842476
-
Diagnostic value of electrocardiograph v and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population
-
Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Millaire A, Carrier L, Bonne G, Tesson F, Richard P, Bouhour J-B, Schwanz K, Komajda M. Diagnostic value of electrocardiograph v and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population. Circulation. 1997;96:214-219.
-
(1997)
Circulation
, vol.96
, pp. 214-219
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagege, A.5
Millaire, A.6
Carrier, L.7
Bonne, G.8
Tesson, F.9
Richard, P.10
Bouhour, J.-B.11
Schwanz, K.12
Komajda, M.13
-
23
-
-
0025320590
-
Relation between extent of left ventricular hypertrophy and diastolic filling abnormalities in hypertrophic cardiomyopathy
-
Spirito P, Maron BJ. Relation between extent of left ventricular hypertrophy and diastolic filling abnormalities in hypertrophic cardiomyopathy. J Am Coll Cardiol. 1990;15:808-813.
-
(1990)
J Am Coll Cardiol
, vol.15
, pp. 808-813
-
-
Spirito, P.1
Maron, B.J.2
-
24
-
-
8544283018
-
Penetrance of familial hypertrophic cardiomyopathy
-
Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour J-B, Mallet A, Feingold J, Schwanz K, Komajda M. Penetrance of familial hypertrophic cardiomyopathy. Genet Count. 1997;8:107-114.
-
(1997)
Genet Count
, vol.8
, pp. 107-114
-
-
Charron, P.1
Carrier, L.2
Dubourg, O.3
Tesson, F.4
Desnos, M.5
Richard, P.6
Bonne, G.7
Guicheney, P.8
Hainque, B.9
Bouhour, J.-B.10
Mallet, A.11
Feingold, J.12
Schwanz, K.13
Komajda, M.14
-
25
-
-
0019165493
-
Echocardiographic measurements in normal subjects from infancy to old age
-
Henry WL, Gardin JM, Ware JH. Echocardiographic measurements in normal subjects from infancy to old age. Circulation, 1980;62:1054-1066.
-
(1980)
Circulation
, vol.62
, pp. 1054-1066
-
-
Henry, W.L.1
Gardin, J.M.2
Ware, J.H.3
-
26
-
-
0014300851
-
Point score system for the ECG diagnosis of left ventricular hypertrophy
-
Romhilt DW, Estes EH. Point score system for the ECG diagnosis of left ventricular hypertrophy. Am Heart J. 1968;75:752-758.
-
(1968)
Am Heart J
, vol.75
, pp. 752-758
-
-
Romhilt, D.W.1
Estes, E.H.2
-
27
-
-
33845382806
-
Non parametric estimation from incomplete observations
-
Kaplan EL, Meier P. Non parametric estimation from incomplete observations. J Am Stat Assoc. 1958;53:457-481.
-
(1958)
J am Stat Assoc
, vol.53
, pp. 457-481
-
-
Kaplan, E.L.1
Meier, P.2
-
28
-
-
0030852878
-
Novel splice site donor mutation in the cardiac myosin binding protein C gene in familial hypertrophic cardiomyopathy
-
Rotbauer W, Gautel M, Zeheleln J, Labeit S, Franz WM, Fischer C, Volrath B, Mall G, Dietz R, Kubler W, Katus HU. Novel splice site donor mutation in the cardiac myosin binding protein C gene in familial hypertrophic cardiomyopathy. J Clin Invest. 1997;100:475-482.
-
(1997)
J Clin Invest
, vol.100
, pp. 475-482
-
-
Rotbauer, W.1
Gautel, M.2
Zeheleln, J.3
Labeit, S.4
Franz, W.M.5
Fischer, C.6
Volrath, B.7
Mall, G.8
Dietz, R.9
Kubler, W.10
Katus, H.U.11
-
29
-
-
0010585135
-
Familial hypertrophic cardiomyopathy: A genetic model of cardiac hypertrophy
-
Watkins H, Seidman JG, Seidman CE. Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy. Hum Mol Genet. 1995;91:532-540.
-
(1995)
Hum Mol Genet
, vol.91
, pp. 532-540
-
-
Watkins, H.1
Seidman, J.G.2
Seidman, C.E.3
-
30
-
-
0023245104
-
Absence of progression of left ventricular hypertrophy in adult patients with hypertrophic cardiomyopathy
-
Spirito P, Maron BJ, Absence of progression of left ventricular hypertrophy in adult patients with hypertrophic cardiomyopathy. J Am Coll Cardiol. 1987;9:1013-1017.
-
(1987)
J am Coll Cardiol
, vol.9
, pp. 1013-1017
-
-
Spirito, P.1
Maron, B.J.2
-
31
-
-
0028140230
-
Genotype-phenotype correlations in hypertrophic cardiomyopathy: Insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations
-
Fananapazir L, Epstein ND. Genotype-phenotype correlations in hypertrophic cardiomyopathy: insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations. Circulation. 1994;89:22-32.
-
(1994)
Circulation
, vol.89
, pp. 22-32
-
-
Fananapazir, L.1
Epstein, N.D.2
-
32
-
-
8044244822
-
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy
-
Forissier J-F, Carrier L, Farza H, Bonne G, Bercovici J, Richard P, Hainque B, Townsend P, Yacoub MH, Faure S, Dubourg O, Millaire A, Hagege AA, Desnos M, Komajda M, Schwanz K. Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy. Circulation. 1996;94:3069-3073.
-
(1996)
Circulation
, vol.94
, pp. 3069-3073
-
-
Forissier, J.-F.1
Carrier, L.2
Farza, H.3
Bonne, G.4
Bercovici, J.5
Richard, P.6
Hainque, B.7
Townsend, P.8
Yacoub, M.H.9
Faure, S.10
Dubourg, O.11
Millaire, A.12
Hagege, A.A.13
Desnos, M.14
Komajda, M.15
Schwanz, K.16
-
33
-
-
0001469979
-
P-wave analysis in valvular heart disease
-
Morris JJ, Estes EH, Whalen RE, Thompson HK, Mclntosh HD. P-wave analysis in valvular heart disease. Circulation. 1964;29:242-252.
-
(1964)
Circulation
, vol.29
, pp. 242-252
-
-
Morris, J.J.1
Estes, E.H.2
Whalen, R.E.3
Thompson, H.K.4
Mclntosh, H.D.5
|