-
1
-
-
0029864693
-
Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of Cardiomyopathies
-
Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of Cardiomyopathies. Circulation. 1996;93:841-842.
-
(1996)
Circulation
, vol.93
, pp. 841-842
-
-
-
2
-
-
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
-
3
-
-
0022498091
-
Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy
-
Maron BJ, Spirito P, Wesley Y, Arce J. Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy. N Engl J Med. 1986;315:610-614.
-
(1986)
N Engl J Med.
, vol.315
, pp. 610-614
-
-
Maron, B.J.1
Spirito, P.2
Wesley, Y.3
Arce, J.4
-
4
-
-
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
-
5
-
-
0025279744
-
Hypertrophic cardiomyopathy without hypertrophy: Two families with myocardial disarray in the absence of increased myocardial mass
-
McKenna WJ, Stewart JT, Nihoyannopoulos P, McGinty F, Davies MJ. Hypertrophic cardiomyopathy without hypertrophy: two families with myocardial disarray in the absence of increased myocardial mass. Br Heart J. 1990;63:287-290.
-
(1990)
Br Heart J.
, vol.63
, pp. 287-290
-
-
McKenna, W.J.1
Stewart, J.T.2
Nihoyannopoulos, P.3
McGinty, F.4
Davies, M.J.5
-
6
-
-
0025128264
-
Genetic evidence of dissociation (generational skips) of electrical from morphologic forms of hypertrophic cardiomyopathy
-
Epstein ND, Lin HJ, Fananapazir L. Genetic evidence of dissociation (generational skips) of electrical from morphologic forms of hypertrophic cardiomyopathy. Am J Cardiol. 1990;66:627-631.
-
(1990)
Am J Cardiol.
, vol.66
, pp. 627-631
-
-
Epstein, N.D.1
Lin, H.J.2
Fananapazir, L.3
-
7
-
-
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
-
8
-
-
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
-
9
-
-
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, Schwartz 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
Schwartz, K.14
-
10
-
-
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
-
11
-
-
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 He, Hassenzadeh S, Master SR, Chang A, Dalakas MC, Rayment I, Sellers JR, Fananapazir L, Epstein ND. 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. 1996;13:63-69.
-
(1996)
Nat Genet.
, vol.13
, pp. 63-69
-
-
Poetter, K.1
He, J.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
-
12
-
-
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, Bercovici J, Hengstenberg C, Al-Mahdawi S, Isnard R, Hagège A, Bouhour JB, Desnos M, Beckmann JS, Weissenbach J, Schwartz 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
Bercovici, J.8
Hengstenberg, C.9
Al-Mahdawi, S.10
Isnard, R.11
Hagège, A.12
Bouhour, J.B.13
Desnos, M.14
Beckmann, J.S.15
Weissenbach, J.16
Schwartz, K.17
Guicheney, P.18
-
13
-
-
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
-
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
-
-
0028167795
-
The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene
-
Al-Mahdawi S, Chamberlain S, Chojnowska L, Michalak E, Nihoyannopoulos P, Ryan M, Kusnierczyk B, French J, Gilligan D, Cleland J, Williamson R, Ruzyllo W, Oakley C. The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene. Br Heart J. 1994;72:105-111.
-
(1994)
Br Heart J.
, vol.72
, pp. 105-111
-
-
Al-Mahdawi, S.1
Chamberlain, S.2
Chojnowska, L.3
Michalak, E.4
Nihoyannopoulos, P.5
Ryan, M.6
Kusnierczyk, B.7
French, J.8
Gilligan, D.9
Cleland, J.10
Williamson, R.11
Ruzyllo, W.12
Oakley, C.13
-
16
-
-
0029014579
-
Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac β-myosin heavy chain gene mutations
-
Posen B, Moolman JC, Corfield VA, Brink PA. Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac β-myosin heavy chain gene mutations. Br Heart J. 1995;74:40-46.
-
(1995)
Br Heart J.
, vol.74
, pp. 40-46
-
-
Posen, B.1
Moolman, J.C.2
Corfield, V.A.3
Brink, P.A.4
-
17
-
-
0028145776
-
Identification of a mutation 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, Schwartz K. Identification of a mutation 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
Schwartz, K.9
-
18
-
-
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, Schwartz 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
Schwartz, K.7
Guicheney, P.8
-
19
-
-
4243207053
-
Genomic organisation of human cardiac troponin T gene: Relevance in mutation analysis in familial hypertrophic cardiomyopathy
-
Abstract
-
Farza H, Townsend PJ, Carrier L, Forrissier JF, Komajda M, Yacoub MH, Schwartz K. Genomic organisation of human cardiac troponin T gene: relevance in mutation analysis in familial hypertrophic cardiomyopathy. J Mol Cell Cardiol. 1996;28:A35. Abstract.
-
(1996)
J Mol Cell Cardiol.
, vol.28
-
-
Farza, H.1
Townsend, P.J.2
Carrier, L.3
Forrissier, J.F.4
Komajda, M.5
Yacoub, M.H.6
Schwartz, K.7
-
20
-
-
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, Schwartz 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
Schwartz, K.12
Komajda, M.13
-
21
-
-
0018231715
-
Recommendations regarding quantification in M-mode echocardiography: Results of a survey of echocardiographic measurements
-
Sahn DJ, DeMaria A, Kisslo J, Weyman A. Recommendations regarding quantification in M-mode echocardiography: results of a survey of echocardiographic measurements. Circulation. 1978;58: 1072-1083.
-
(1978)
Circulation
, vol.58
, pp. 1072-1083
-
-
Sahn, D.J.1
Demaria, A.2
Kisslo, J.3
Weyman, A.4
-
22
-
-
0021346026
-
Patterns of inheritance in hypertrophic cardiomyopathy: Assessment by M-mode and two-dimensional echocardiography
-
Maron BJ, Nichols PF III, Pickle LW, Wesley YE, Mulvihill JJ. Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography. Am J Cardiol. 1984;53:1087-1094.
-
(1984)
Am J Cardiol.
, vol.53
, pp. 1087-1094
-
-
Maron, B.J.1
Nichols P.F. III2
Pickle, L.W.3
Wesley, Y.E.4
Mulvihill, J.J.5
-
23
-
-
0024551305
-
Relation between extent of left ventricular hypertrophy and age in hypertrophic cardiomyopathy
-
Spirito P, Maron BJ. Relation between extent of left ventricular hypertrophy and age in hypertrophic cardiomyopathy. J Am Coll Cardiol. 1989;13:820-823.
-
(1989)
J Am Coll Cardiol.
, vol.13
, pp. 820-823
-
-
Spirito, P.1
Maron, B.J.2
-
24
-
-
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
-
25
-
-
0001469979
-
P-wave analysis in valvular heart disease
-
Morris JJ, Estes EH, Whalen RE, Thompson HK, McIntosh 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
McIntosh, H.D.5
-
26
-
-
0018088078
-
Electrocardiographic findings in patients with obstructive and nonobstructive hypertrophic cardiomyopathy
-
Savage DD, Seides SF, Clark CE, Henry WL, Maron BJ, Robinson FC, Epstein SE. Electrocardiographic findings in patients with obstructive and nonobstructive hypertrophic cardiomyopathy. Circulation. 1978;58:402-408.
-
(1978)
Circulation
, vol.58
, pp. 402-408
-
-
Savage, D.D.1
Seides, S.F.2
Clark, C.E.3
Henry, W.L.4
Maron, B.J.5
Robinson, F.C.6
Epstein, S.E.7
-
28
-
-
0020685442
-
Relation of electrocardiographic abnormalities and patterns of left ventricular hypertrophy identified by 2-dimensional echocardiography in patients with hypertrophic cardiomyopathy
-
Maron BJ, Wolfson JK, Ciro E, Spirito P. Relation of electrocardiographic abnormalities and patterns of left ventricular hypertrophy identified by 2-dimensional echocardiography in patients with hypertrophic cardiomyopathy. Am J Cardiol. 1982;51:189-194.
-
(1982)
Am J Cardiol.
, vol.51
, pp. 189-194
-
-
Maron, B.J.1
Wolfson, J.K.2
Ciro, E.3
Spirito, P.4
-
29
-
-
0029119043
-
The standard electrocardiogram as a screening test for hypertrophic cardiomyopathy
-
Ryan MK, Cleland JGF, French JA, Joshi J, Choudhury L, Chojnowska L, Michalak E, Al-Mahdawi S, Nihoyannopoulos P, Oakley CM. The standard electrocardiogram as a screening test for hypertrophic cardiomyopathy. Am J Cardiol. 1995;76:689-694.
-
(1995)
Am J Cardiol.
, vol.76
, pp. 689-694
-
-
Ryan, M.K.1
Cleland, J.G.F.2
French, J.A.3
Joshi, J.4
Choudhury, L.5
Chojnowska, L.6
Michalak, E.7
Al-Mahdawi, S.8
Nihoyannopoulos, P.9
Oakley, C.M.10
-
30
-
-
0027209383
-
Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene
-
Solomon ST, Wolff S, Watkins H, Ridker PM, Come P, McKenna WJ, Seidman CE, Lee RT. Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene. J Am Coll Cardiol. 1993;22:498-505.
-
(1993)
J Am Coll Cardiol.
, vol.22
, pp. 498-505
-
-
Solomon, S.T.1
Wolff, S.2
Watkins, H.3
Ridker, P.M.4
Come, P.5
McKenna, W.J.6
Seidman, C.E.7
Lee, R.T.8
-
31
-
-
0025274840
-
Determinants of sensitivity and specificity of electrocardiographic criteria for left ventricular hypertrophy
-
Levy D, Labib SB, Anderson KM, Christiansen JC, Kannel WB, Castelli WP. Determinants of sensitivity and specificity of electrocardiographic criteria for left ventricular hypertrophy. Circulation. 1990;81:815-820.
-
(1990)
Circulation
, vol.81
, pp. 815-820
-
-
Levy, D.1
Labib, S.B.2
Anderson, K.M.3
Christiansen, J.C.4
Kannel, W.B.5
Castelli, W.P.6
-
32
-
-
0025305767
-
Is the electrocardiogram still useful for detection of left ventricular hypertrophy?
-
Devereux RB. Is the electrocardiogram still useful for detection of left ventricular hypertrophy? Circulation. 1990;81:1144-1146.
-
(1990)
Circulation
, vol.81
, pp. 1144-1146
-
-
Devereux, R.B.1
-
33
-
-
0023258399
-
Inheritance of hypertrophic cardiomyopathy: A cross sectional and M mode echocardiographic study of 50 families
-
Greaves SC, Roche AHG, Neutze JM, Whitlock RML, Veale AMO. Inheritance of hypertrophic cardiomyopathy: a cross sectional and M mode echocardiographic study of 50 families. Br Heart J. 1987;58:259-266.
-
(1987)
Br Heart J.
, vol.58
, pp. 259-266
-
-
Greaves, S.C.1
Roche, A.H.G.2
Neutze, J.M.3
Whitlock, R.M.L.4
Veale, A.M.O.5
-
34
-
-
0028849972
-
Phenotypic spectrum and patterns of left ventricular hypertrophy in hypertrophic cardiomyopathy: Morphological observations and significance as assessed by two-dimensional echocardiography in 600 patients
-
Klues HG, Schiffers A, Maron BJ. Phenotypic spectrum and patterns of left ventricular hypertrophy in hypertrophic cardiomyopathy: morphological observations and significance as assessed by two-dimensional echocardiography in 600 patients. J Am Coll Cardiol. 1995;26:1699-1708.
-
(1995)
J Am Coll Cardiol.
, vol.26
, pp. 1699-1708
-
-
Klues, H.G.1
Schiffers, A.2
Maron, B.J.3
-
35
-
-
0020034028
-
Mode of inheritance of hypertrophic cardiomyopathy in Iceland: Echographic study
-
Bjarnason I, Jonsson S, Hardarson T. Mode of inheritance of hypertrophic cardiomyopathy in Iceland: echographic study. Br Heart J. 1982,47:122-129.
-
(1982)
Br Heart J.
, vol.47
, pp. 122-129
-
-
Bjarnason, I.1
Jonsson, S.2
Hardarson, T.3
-
36
-
-
0023269245
-
Occurrence and significance of progressive left ventricular thinning and relative cavity dilatation in hypertrophic cardiomyopathy
-
Spirito P, Maron BJ, Bonow RO, Epstein SE. Occurrence and significance of progressive left ventricular thinning and relative cavity dilatation in hypertrophic cardiomyopathy. Am J Cardiol. 1987;59:123-129.
-
(1987)
Am J Cardiol.
, vol.59
, pp. 123-129
-
-
Spirito, P.1
Maron, B.J.2
Bonow, R.O.3
Epstein, S.E.4
-
37
-
-
0015914247
-
Familial prevalence and genetic transmission of idiopathic subaortic stenosis
-
Clark CE, Henry WL, Epstein SE. Familial prevalence and genetic transmission of idiopathic subaortic stenosis. N Engl J Med. 1973; 289:709-714.
-
(1973)
N Engl J Med.
, vol.289
, pp. 709-714
-
-
Clark, C.E.1
Henry, W.L.2
Epstein, S.E.3
-
38
-
-
0020561948
-
Distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy: A two dimensional echocardiographic study
-
Shapiro LM, McKenna WJ. Distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy: a two dimensional echocardiographic study. J Am Coll Cardiol. 1983;2:437-444.
-
(1983)
J Am Coll Cardiol.
, vol.2
, pp. 437-444
-
-
Shapiro, L.M.1
McKenna, W.J.2
-
39
-
-
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
-
40
-
-
0018604358
-
Echocardiographic measurements in normal subjects: Evaluation in an adult population without clinically apparent heart disease
-
Gardin JM, Henry WL, Savage DD, Ware JH, Burn C, Borer JS.Echocardiographic measurements in normal subjects: evaluation in an adult population without clinically apparent heart disease. J Clin Ultrasound. 1979;7:439-447.
-
(1979)
J Clin Ultrasound
, vol.7
, pp. 439-447
-
-
Gardin, J.M.1
Henry, W.L.2
Savage, D.D.3
Ware, J.H.4
Burn, C.5
Borer, J.S.6
-
41
-
-
0018834621
-
M mode echocardiography in hypertrophic cardiomyopathy: Diagnostic criteria and prediction of obstruction
-
Doi YL, McKenna WJ, Gerhrke J, Oakley CM, Goodwin JF. M mode echocardiography in hypertrophic cardiomyopathy: diagnostic criteria and prediction of obstruction. Am J Cardiol. 1980;45:6-14.
-
(1980)
Am J Cardiol.
, vol.45
, pp. 6-14
-
-
Doi, Y.L.1
McKenna, W.J.2
Gerhrke, J.3
Oakley, C.M.4
Goodwin, J.F.5
|