-
1
-
-
0037070514
-
Hypertrophic cardiomyopathy: a systematic review
-
Maron B.J. Hypertrophic cardiomyopathy: a systematic review. JAMA 287 (2002) 1308-1320
-
(2002)
JAMA
, vol.287
, pp. 1308-1320
-
-
Maron, B.J.1
-
2
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance A.A., Kass S., Tanigawa G., Vosberg H., McKenna W., Seidman C.E., and Seidman J.G. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell 62 (1990) 999-1006
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
3
-
-
0024522726
-
Hypertrophic cardiomyopathy in the elderly. Distinctions from the young based on cardiac shape
-
Lever H.M., Karam R.F., Currie P.J., and Healy B.P. Hypertrophic cardiomyopathy in the elderly. Distinctions from the young based on cardiac shape. Circulation 79 (1989) 580-589
-
(1989)
Circulation
, vol.79
, pp. 580-589
-
-
Lever, H.M.1
Karam, R.F.2
Currie, P.J.3
Healy, B.P.4
-
4
-
-
0027209383
-
Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene
-
Solomon S.D., Wolff S., Watkins H., Ridker P.M., Come P., McKenna W.J., Seidman C.E., and Lee R.T. Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene. J. Am. Coll. Cardiol. 22 (1993) 498-505
-
(1993)
J. Am. Coll. Cardiol.
, vol.22
, pp. 498-505
-
-
Solomon, S.D.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
-
5
-
-
33645655544
-
Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations
-
Binder J., Ommen S.R., Gersh B.J., Van Driest S.L., Tajik A.J., Nishimura R.A., and Ackerman M.J. Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations. Mayo Clin. Proc. 81 (2006) 459-467
-
(2006)
Mayo Clin. Proc.
, vol.81
, pp. 459-467
-
-
Binder, J.1
Ommen, S.R.2
Gersh, B.J.3
Van Driest, S.L.4
Tajik, A.J.5
Nishimura, R.A.6
Ackerman, M.J.7
-
6
-
-
4043081356
-
Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy
-
Van Driest S.L., Jaeger M.A., Ommen S.R., Will M.L., Gersh B.J., Tajik A.J., and Ackerman M.J. Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 44 (2004) 602-610
-
(2004)
J. Am. Coll. Cardiol.
, vol.44
, pp. 602-610
-
-
Van Driest, S.L.1
Jaeger, M.A.2
Ommen, S.R.3
Will, M.L.4
Gersh, B.J.5
Tajik, A.J.6
Ackerman, M.J.7
-
7
-
-
7044264544
-
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
-
Van Driest S.L., Vasile V.C., Ommen S.R., Will M.L., Gersh B.J., Nishimura R.A., Tajik A.J., and Ackerman M.J. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 44 (2004) 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
Gersh, B.J.5
Nishimura, R.A.6
Tajik, A.J.7
Ackerman, M.J.8
-
8
-
-
0041663609
-
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
-
Van Driest S.L., Ellsworth E.G., Ommen S.R., Tajik A.J., Gersh B.J., and Ackerman M.J. Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy. Circulation 108 (2003) 445-451
-
(2003)
Circulation
, vol.108
, pp. 445-451
-
-
Van Driest, S.L.1
Ellsworth, E.G.2
Ommen, S.R.3
Tajik, A.J.4
Gersh, B.J.5
Ackerman, M.J.6
-
9
-
-
33646049669
-
Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin
-
Bos J.M., Poley R.N., Ny M., Tester D.J., Xu X., Vatta M., Towbin J.A., Gersh B.J., Ommen S.R., and Ackerman M.J. Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin. Mol. Genet. Metab. 88 (2006) 78-85
-
(2006)
Mol. Genet. Metab.
, vol.88
, pp. 78-85
-
-
Bos, J.M.1
Poley, R.N.2
Ny, M.3
Tester, D.J.4
Xu, X.5
Vatta, M.6
Towbin, J.A.7
Gersh, B.J.8
Ommen, S.R.9
Ackerman, M.J.10
-
10
-
-
32044458438
-
Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy
-
Vasile V.C., Will M.L., Ommen S.R., Edwards W.D., Olson T.M., and Ackerman M.J. Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy. Mol. Genet. Metab. 87 (2006) 169-174
-
(2006)
Mol. Genet. Metab.
, vol.87
, pp. 169-174
-
-
Vasile, V.C.1
Will, M.L.2
Ommen, S.R.3
Edwards, W.D.4
Olson, T.M.5
Ackerman, M.J.6
-
11
-
-
9644281144
-
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy
-
Hayashi T., Arimura T., Itoh-Satoh M., Ueda K., Hohda S., Inagaki N., Takahashi M., Hori H., Yasunami M., Nishi H., Koga Y., Nakamura H., Matsuzaki M., Choi B.Y., Bae S.W., You C.W., Han K.H., Park J.E., Knoll R., Hoshijima M., Chien K.R., and Kimura A. Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy. J. Am. Coll. Cardiol. 44 (2004) 2192-2201
-
(2004)
J. Am. Coll. Cardiol.
, vol.44
, pp. 2192-2201
-
-
Hayashi, T.1
Arimura, T.2
Itoh-Satoh, M.3
Ueda, K.4
Hohda, S.5
Inagaki, N.6
Takahashi, M.7
Hori, H.8
Yasunami, M.9
Nishi, H.10
Koga, Y.11
Nakamura, H.12
Matsuzaki, M.13
Choi, B.Y.14
Bae, S.W.15
You, C.W.16
Han, K.H.17
Park, J.E.18
Knoll, R.19
Hoshijima, M.20
Chien, K.R.21
Kimura, A.22
more..
-
12
-
-
0037453074
-
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy
-
Geier C., Perrot A., Ozcelik C., Binner P., Counsell D., Hoffmann K., Pilz B., Martiniak Y., Gehmlich K., van der Ven P.F., Furst D.O., Vornwald A., von Hodenberg E., Nurnberg P., Scheffold T., Dietz R., and Osterziel K.J. Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy. Circulation 107 (2003) 1390-1395
-
(2003)
Circulation
, vol.107
, pp. 1390-1395
-
-
Geier, C.1
Perrot, A.2
Ozcelik, C.3
Binner, P.4
Counsell, D.5
Hoffmann, K.6
Pilz, B.7
Martiniak, Y.8
Gehmlich, K.9
van der Ven, P.F.10
Furst, D.O.11
Vornwald, A.12
von Hodenberg, E.13
Nurnberg, P.14
Scheffold, T.15
Dietz, R.16
Osterziel, K.J.17
-
13
-
-
33646850881
-
A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathy
-
Vasile V.C., Ommen S.R., Edwards W.D., and Ackerman M.J. A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathy. Biochem. Biophys. Res. Comm. 345 (2006) 998-1003
-
(2006)
Biochem. Biophys. Res. Comm.
, vol.345
, pp. 998-1003
-
-
Vasile, V.C.1
Ommen, S.R.2
Edwards, W.D.3
Ackerman, M.J.4
-
14
-
-
0142058043
-
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis
-
Mohapatra B., Jimenez S., Lin J.H., Bowles K.R., Coveler K.J., Marx J.G., Chrisco M.A., Murphy R.T., Lurie P.R., Schwartz R.J., Elliott P.M., Vatta M., McKenna W., Towbin J.A., and Bowles N.E. Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis. Mol. Genet. Metab. 80 (2003) 207-215
-
(2003)
Mol. Genet. Metab.
, vol.80
, pp. 207-215
-
-
Mohapatra, B.1
Jimenez, S.2
Lin, J.H.3
Bowles, K.R.4
Coveler, K.J.5
Marx, J.G.6
Chrisco, M.A.7
Murphy, R.T.8
Lurie, P.R.9
Schwartz, R.J.10
Elliott, P.M.11
Vatta, M.12
McKenna, W.13
Towbin, J.A.14
Bowles, N.E.15
-
15
-
-
0037192309
-
Metavinculin mutations alter actin interaction in dilated cardiomyopathy
-
Olson T.M., Illenberger S., Kishimoto N.Y., Huttelmaier S., Keating M.T., and Jockusch B.M. Metavinculin mutations alter actin interaction in dilated cardiomyopathy. Circulation 105 (2002) 431-437
-
(2002)
Circulation
, vol.105
, pp. 431-437
-
-
Olson, T.M.1
Illenberger, S.2
Kishimoto, N.Y.3
Huttelmaier, S.4
Keating, M.T.5
Jockusch, B.M.6
-
16
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago M., Sharma S.D., DePalma S.R., Solomon S., Sharma P., McDonough B., Smoot L., Mullen M.P., Woolf P.K., Wigle E.D., Seidman J.G., and Seidman C.E. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N. Engl. J. Med. 343 (2000) 1688-1696
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
McDonough, B.6
Smoot, L.7
Mullen, M.P.8
Woolf, P.K.9
Wigle, E.D.10
Seidman, J.G.11
Seidman, C.E.12
-
17
-
-
0033799445
-
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy
-
Olson T.M., Doan T.P., Kishimoto N.Y., Whitby F.G., Ackerman M.J., and Fananapazir L. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 32 (2000) 1687-1694
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, pp. 1687-1694
-
-
Olson, T.M.1
Doan, T.P.2
Kishimoto, N.Y.3
Whitby, F.G.4
Ackerman, M.J.5
Fananapazir, L.6
-
18
-
-
0034971165
-
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
-
Olson T.M., Kishimoto N.Y., Whitby F.G., and Michels V.V. Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy. J. Mol. Cell. Cardiol. 33 (2001) 723-732
-
(2001)
J. Mol. Cell. Cardiol.
, vol.33
, pp. 723-732
-
-
Olson, T.M.1
Kishimoto, N.Y.2
Whitby, F.G.3
Michels, V.V.4
-
19
-
-
0036478897
-
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
-
Gerull B., Gramlich M., Atherton J., McNabb M., Trombitas K., Sasse-Klaassen S., Seidman J.G., Seidman C., Granzier H., Labeit S., Frenneaux M., and Thierfelder L. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy. Nat. Genet. 30 (2002) 201-204
-
(2002)
Nat. Genet.
, vol.30
, pp. 201-204
-
-
Gerull, B.1
Gramlich, M.2
Atherton, J.3
McNabb, M.4
Trombitas, 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
-
20
-
-
0036401384
-
Novel mutations in sarcomeric protein genes in dilated cardiomyopathy
-
Daehmlow S., Erdmann J., Knueppel T., Gille C., Froemmel C., Hummel M., Hetzer R., and Regitz-Zagrosek V. Novel mutations in sarcomeric protein genes in dilated cardiomyopathy. Biochem. Biophys. Res. Commun. 298 (2002) 116-120
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.298
, pp. 116-120
-
-
Daehmlow, S.1
Erdmann, J.2
Knueppel, T.3
Gille, C.4
Froemmel, C.5
Hummel, M.6
Hetzer, R.7
Regitz-Zagrosek, V.8
-
21
-
-
0344873698
-
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction
-
Vatta M., Mohapatra B., Jimenez S., Sanchez X., Faulkner G., Perles Z., Sinagra G., Lin J.H., Vu T.M., Zhou Q., Bowles K.R., Di Lenarda A., Schimmenti L., Fox M., Chrisco M.A., Murphy R.T., McKenna W., Elliott P., Bowles N.E., Chen J., Valle G., and Towbin J.A. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J. Am. Coll. Cardiol. 42 (2003) 2014-2027
-
(2003)
J. Am. Coll. Cardiol.
, vol.42
, pp. 2014-2027
-
-
Vatta, M.1
Mohapatra, B.2
Jimenez, S.3
Sanchez, X.4
Faulkner, G.5
Perles, Z.6
Sinagra, G.7
Lin, J.H.8
Vu, T.M.9
Zhou, Q.10
Bowles, K.R.11
Di Lenarda, A.12
Schimmenti, L.13
Fox, M.14
Chrisco, M.A.15
Murphy, R.T.16
McKenna, W.17
Elliott, P.18
Bowles, N.E.19
Chen, J.20
Valle, G.21
Towbin, J.A.22
more..
-
22
-
-
84924110084
-
Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy
-
Zhou Q., Chu P.H., Huang C., Cheng C.F., Martone M.E., Knoll G., Shelton G.D., Evans S., and Chen J. Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy. J. Cell Biol. 155 (2001) 605-612
-
(2001)
J. Cell Biol.
, vol.155
, pp. 605-612
-
-
Zhou, Q.1
Chu, P.H.2
Huang, C.3
Cheng, C.F.4
Martone, M.E.5
Knoll, G.6
Shelton, G.D.7
Evans, S.8
Chen, J.9
-
23
-
-
33744494538
-
The sarcomeric Z-disc: a nodal point in signalling and disease
-
Frank D., Kuhn C., Katus H.A., and Frey N. The sarcomeric Z-disc: a nodal point in signalling and disease. J. Mol. Med. (2006) 1-23
-
(2006)
J. Mol. Med.
, pp. 1-23
-
-
Frank, D.1
Kuhn, C.2
Katus, H.A.3
Frey, N.4
-
24
-
-
1242320058
-
At the crossroads of myocardial signaling: the role of Z-discs in intracellular signaling and cardiac function
-
Pyle W.G., and Solaro R.J. At the crossroads of myocardial signaling: the role of Z-discs in intracellular signaling and cardiac function. Circ. Res. 94 (2004) 296-305
-
(2004)
Circ. Res.
, vol.94
, pp. 296-305
-
-
Pyle, W.G.1
Solaro, R.J.2
-
25
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
Knoll R., Hoshijima M., Hoffman H.M., Person V., Lorenzen-Schmidt I., Bang M.L., Hayashi T., Shiga N., Yasukawa H., Schaper W., McKenna W., Yokoyama M., Schork N.J., Omens J.H., McCulloch A.D., Kimura A., Gregorio C.C., Poller W., Schaper J., Schultheiss H.P., and Chien K.R. The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell 111 (2002) 943-955
-
(2002)
Cell
, vol.111
, pp. 943-955
-
-
Knoll, R.1
Hoshijima, M.2
Hoffman, H.M.3
Person, V.4
Lorenzen-Schmidt, I.5
Bang, M.L.6
Hayashi, T.7
Shiga, N.8
Yasukawa, H.9
Schaper, W.10
McKenna, W.11
Yokoyama, M.12
Schork, N.J.13
Omens, J.H.14
McCulloch, A.D.15
Kimura, A.16
Gregorio, C.C.17
Poller, W.18
Schaper, J.19
Schultheiss, H.P.20
Chien, K.R.21
more..
-
26
-
-
20044382630
-
Yield of genetic testing in hypertrophic cardiomyopathy
-
Van Driest S.L., Ommen S.R., Tajik A.J., Gersh B.J., and Ackerman M.J. Yield of genetic testing in hypertrophic cardiomyopathy. Mayo Clin. Proc. 80 (2005) 739-744
-
(2005)
Mayo Clin. Proc.
, vol.80
, pp. 739-744
-
-
Van Driest, S.L.1
Ommen, S.R.2
Tajik, A.J.3
Gersh, B.J.4
Ackerman, M.J.5
-
27
-
-
0035872209
-
Mutations in the gamma(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., Oliveira M., Broxholme J., Kerr B., Salmon A., Ostman-Smith I., and Watkins H. Mutations in the gamma(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 (2001) 1215-1220
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1215-1220
-
-
Blair, E.1
Redwood, C.2
Ashrafian, H.3
Oliveira, M.4
Broxholme, J.5
Kerr, B.6
Salmon, A.7
Ostman-Smith, I.8
Watkins, H.9
-
28
-
-
19944434362
-
Glycogen storage diseases presenting as hypertrophic cardiomyopathy
-
Arad M., Maron B.J., Gorham J.M., Johnson Jr. W.H., Saul J.P., Perez-Atayde A.R., Spirito P., Wright G.B., Kanter R.J., Seidman C.E., and Seidman J.G. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N. Engl. J. Med. 352 (2005) 362-372
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 362-372
-
-
Arad, M.1
Maron, B.J.2
Gorham, J.M.3
Johnson Jr., W.H.4
Saul, J.P.5
Perez-Atayde, A.R.6
Spirito, P.7
Wright, G.B.8
Kanter, R.J.9
Seidman, C.E.10
Seidman, J.G.11
-
29
-
-
1842579393
-
Hypertrophy of the heart: a new therapeutic target?
-
Frey N., Katus H.A., Olson E.N., and Hill J.A. Hypertrophy of the heart: a new therapeutic target?. Circulation 109 (2004) 1580-1589
-
(2004)
Circulation
, vol.109
, pp. 1580-1589
-
-
Frey, N.1
Katus, H.A.2
Olson, E.N.3
Hill, J.A.4
-
30
-
-
27644562178
-
Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy
-
Perkins M.J., Van Driest S.L., Ellsworth E.G., Will M.L., Gersh B.J., Ommen S.R., and Ackerman M.J. Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy. Eur. Heart J. 26 (2005) 2457-2462
-
(2005)
Eur. Heart J.
, vol.26
, pp. 2457-2462
-
-
Perkins, M.J.1
Van Driest, S.L.2
Ellsworth, E.G.3
Will, M.L.4
Gersh, B.J.5
Ommen, S.R.6
Ackerman, M.J.7
-
31
-
-
0030827949
-
Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifs
-
Xia H., Winokur S.T., Kuo W.L., Altherr M.R., and Bredt D.S. Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifs. J. Cell Biol. 139 (1997) 507-515
-
(1997)
J. Cell Biol.
, vol.139
, pp. 507-515
-
-
Xia, H.1
Winokur, S.T.2
Kuo, W.L.3
Altherr, M.R.4
Bredt, D.S.5
-
32
-
-
0032997340
-
Alpha actinin-CapZ, an anchoring complex for thin filaments in Z-line
-
Papa I., Astier C., Kwiatek O., Raynaud F., Bonnal C., Lebart M.C., Roustan C., and Benyamin Y. Alpha actinin-CapZ, an anchoring complex for thin filaments in Z-line. J. Muscle Res. Cell Motil. 20 (1999) 187-197
-
(1999)
J. Muscle Res. Cell Motil.
, vol.20
, pp. 187-197
-
-
Papa, I.1
Astier, C.2
Kwiatek, O.3
Raynaud, F.4
Bonnal, C.5
Lebart, M.C.6
Roustan, C.7
Benyamin, Y.8
-
33
-
-
0032532666
-
Inhibition of norepinephrine-induced cardiac hypertrophy in s100beta transgenic mice
-
Tsoporis J.N., Marks A., Kahn H.J., Butany J.W., Liu P.P., O'Hanlon D., and Parker T.G. Inhibition of norepinephrine-induced cardiac hypertrophy in s100beta transgenic mice. J. Clin. Invest. 102 (1998) 1609-1616
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1609-1616
-
-
Tsoporis, J.N.1
Marks, A.2
Kahn, H.J.3
Butany, J.W.4
Liu, P.P.5
O'Hanlon, D.6
Parker, T.G.7
|