-
1
-
-
0028918471
-
Cardiac involvement in mitochondrial diseases: a study on 17 patients with documented mitochondrial DNA-defects
-
Anan R., Nakagawa M., Miyata M., et al. Cardiac involvement in mitochondrial diseases: a study on 17 patients with documented mitochondrial DNA-defects. Circulation 91 (1995) 955-961
-
(1995)
Circulation
, vol.91
, pp. 955-961
-
-
Anan, R.1
Nakagawa, M.2
Miyata, M.3
-
2
-
-
0037276860
-
The heart in human dystrophinopathies
-
Finsterer J., and Stöllberger C. The heart in human dystrophinopathies. Cardiology 99 (2003) 1-19
-
(2003)
Cardiology
, vol.99
, pp. 1-19
-
-
Finsterer, J.1
Stöllberger, C.2
-
3
-
-
0033662464
-
Cardiac involvement in primary myopathies
-
Finsterer J., and Stöllberger C. Cardiac involvement in primary myopathies. Cardiology 94 (2000) 1-11
-
(2000)
Cardiology
, vol.94
, pp. 1-11
-
-
Finsterer, J.1
Stöllberger, C.2
-
4
-
-
0037304994
-
107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th-9th June 2002, Naarden, the Netherlands
-
Bushby K., Muntoni F., and Bourke J.P. 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th-9th June 2002, Naarden, the Netherlands. Neuromuscul Disord 13 (2003) 166-172
-
(2003)
Neuromuscul Disord
, vol.13
, pp. 166-172
-
-
Bushby, K.1
Muntoni, F.2
Bourke, J.P.3
-
5
-
-
0028819577
-
Evaluation of the cardiomyopathy in Becker muscular dystrophy
-
Nigro G., Comi L.I., Politano L., Limongelli F.M., Nigro V., and De Rimini M.L. Evaluation of the cardiomyopathy in Becker muscular dystrophy. Muscle Nerve 18 (1995) 283-291
-
(1995)
Muscle Nerve
, vol.18
, pp. 283-291
-
-
Nigro, G.1
Comi, L.I.2
Politano, L.3
Limongelli, F.M.4
Nigro, V.5
De Rimini, M.L.6
-
6
-
-
0031114590
-
Cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy
-
Finsterer J., Stöllberger C., Keller H., Slany J., and Mamoli B. Cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy. Herz 22 (1997) 96-103
-
(1997)
Herz
, vol.22
, pp. 96-103
-
-
Finsterer, J.1
Stöllberger, C.2
Keller, H.3
Slany, J.4
Mamoli, B.5
-
7
-
-
21444450805
-
Clinical and molecular aspects of the myotonic dystrophies: a review
-
Machuca-Tzili L., Brook D., and Hilton-Jones D. Clinical and molecular aspects of the myotonic dystrophies: a review. Muscle Nerve 32 (2005) 1-18
-
(2005)
Muscle Nerve
, vol.32
, pp. 1-18
-
-
Machuca-Tzili, L.1
Brook, D.2
Hilton-Jones, D.3
-
8
-
-
0037160782
-
The muscular dystrophies
-
Emery A.E. The muscular dystrophies. Lancet 359 (2002) 687-695
-
(2002)
Lancet
, vol.359
, pp. 687-695
-
-
Emery, A.E.1
-
9
-
-
0029763025
-
Respiratory chain encephalomyopathies: a diagnostic classification
-
Walker U.A., Collins S., and Byrne E. Respiratory chain encephalomyopathies: a diagnostic classification. Eur Neurol 36 (1996) 260-267
-
(1996)
Eur Neurol
, vol.36
, pp. 260-267
-
-
Walker, U.A.1
Collins, S.2
Byrne, E.3
-
10
-
-
0032417494
-
Progression of cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy during a two year follow-up
-
Stöllberger C., Finsterer J., Keller H., Mamoli B., and Slany J. Progression of cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy during a two year follow-up. Cardiology 90 (1998) 173-179
-
(1998)
Cardiology
, vol.90
, pp. 173-179
-
-
Stöllberger, C.1
Finsterer, J.2
Keller, H.3
Mamoli, B.4
Slany, J.5
-
11
-
-
0035204038
-
Cardiac involvement in myotonic dystrophy, Becker muscular dystrophy and mitochondrial myopathy: a five-year follow-up
-
Finsterer J., Stollberger C., Blazek G., and Spahits E. Cardiac involvement in myotonic dystrophy, Becker muscular dystrophy and mitochondrial myopathy: a five-year follow-up. Can J Cardiol 17 (2001) 1061-1069
-
(2001)
Can J Cardiol
, vol.17
, pp. 1061-1069
-
-
Finsterer, J.1
Stollberger, C.2
Blazek, G.3
Spahits, E.4
-
12
-
-
0031447925
-
ECG abnormalities in myopathies, coronary heart disease and controls
-
Finsterer J., Stöllberger C., Köcher K., and Mamoli B. ECG abnormalities in myopathies, coronary heart disease and controls. Herz 22 (1997) 277-282
-
(1997)
Herz
, vol.22
, pp. 277-282
-
-
Finsterer, J.1
Stöllberger, C.2
Köcher, K.3
Mamoli, B.4
-
13
-
-
0029969701
-
Left ventricular non-compaction in a patient with Becker's muscular dystrophy
-
Stöllberger C., Finsterer J., Blazek G., and Bittner R.E. Left ventricular non-compaction in a patient with Becker's muscular dystrophy. Heart 76 (1996) 380
-
(1996)
Heart
, vol.76
, pp. 380
-
-
Stöllberger, C.1
Finsterer, J.2
Blazek, G.3
Bittner, R.E.4
-
14
-
-
18844434160
-
Cardiac manifestations of muscular dystrophies
-
Perrot A., Spuler S., Geier C., Dietz R., and Osterziel K.J. Cardiac manifestations of muscular dystrophies. Z Kardiol 94 (2005) 312-320
-
(2005)
Z Kardiol
, vol.94
, pp. 312-320
-
-
Perrot, A.1
Spuler, S.2
Geier, C.3
Dietz, R.4
Osterziel, K.J.5
-
15
-
-
8844224764
-
Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1
-
Bassez G., Lazarus A., Desguerre I., et al. Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1. Neurology 63 (2004) 1939-1941
-
(2004)
Neurology
, vol.63
, pp. 1939-1941
-
-
Bassez, G.1
Lazarus, A.2
Desguerre, I.3
-
16
-
-
0032986568
-
Myotonic dystrophy associated with QT prolongation and torsades de pointes
-
Umeda Y., Ikeda U., Yamamoto J., et al. Myotonic dystrophy associated with QT prolongation and torsades de pointes. Clin Cardiol 22 (1999) 136-138
-
(1999)
Clin Cardiol
, vol.22
, pp. 136-138
-
-
Umeda, Y.1
Ikeda, U.2
Yamamoto, J.3
-
17
-
-
0036080610
-
Cardiac involvement and CTG expansion in myotonic dystrophy
-
Merlevede K., Vermander D., Theys P., Legius E., Ector H., and Robberecht W. Cardiac involvement and CTG expansion in myotonic dystrophy. J Neurol 249 (2002) 693-698
-
(2002)
J Neurol
, vol.249
, pp. 693-698
-
-
Merlevede, K.1
Vermander, D.2
Theys, P.3
Legius, E.4
Ector, H.5
Robberecht, W.6
-
18
-
-
0033514985
-
Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy
-
Lazarus A., Varin J., Ounnoughene Z., et al. Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy. Circulation 99 (1999) 1041-1046
-
(1999)
Circulation
, vol.99
, pp. 1041-1046
-
-
Lazarus, A.1
Varin, J.2
Ounnoughene, Z.3
-
19
-
-
0037032260
-
Long-term follow-up of arrhythmias in patients with myotonic dystrophy treated by pacing: a multicenter diagnostic pacemaker study
-
Lazarus A., Varin J., Babuty D., Anselme F., Coste J., and Duboc D. Long-term follow-up of arrhythmias in patients with myotonic dystrophy treated by pacing: a multicenter diagnostic pacemaker study. J Am Coll Cardiol 40 (2002) 1645-1652
-
(2002)
J Am Coll Cardiol
, vol.40
, pp. 1645-1652
-
-
Lazarus, A.1
Varin, J.2
Babuty, D.3
Anselme, F.4
Coste, J.5
Duboc, D.6
-
20
-
-
33645104292
-
Widespread electroanatomic alterations of right cardiac chambers in patients with myotonic dystrophy type 1
-
Russo A.D., Pelargonio G., Parisi Q., et al. Widespread electroanatomic alterations of right cardiac chambers in patients with myotonic dystrophy type 1. J Cardiovasc Electrophysiol 17 (2006) 34-40
-
(2006)
J Cardiovasc Electrophysiol
, vol.17
, pp. 34-40
-
-
Russo, A.D.1
Pelargonio, G.2
Parisi, Q.3
-
21
-
-
19544367095
-
Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy
-
O'Cochlain D.F., Perez-Terzic C., Reyes S., et al. Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy. Hum Mol Genet 13 (2004) 2505-2518
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2505-2518
-
-
O'Cochlain, D.F.1
Perez-Terzic, C.2
Reyes, S.3
-
22
-
-
0842304407
-
Prevalence of structural cardiac abnormalities in patients with myotonic dystrophy type I
-
Bhakta D., Lowe M.R., and Groh W.J. Prevalence of structural cardiac abnormalities in patients with myotonic dystrophy type I. Am Heart J 147 (2004) 224-227
-
(2004)
Am Heart J
, vol.147
, pp. 224-227
-
-
Bhakta, D.1
Lowe, M.R.2
Groh, W.J.3
-
23
-
-
1242271390
-
Subclinical cardiac involvement in myotonic dystrophy manifesting as decreased myocardial Doppler velocities
-
Vinereanu D., Bajaj B.P., Fenton-May J., Rogers M.T., Madler C.F., and Fraser A.G. Subclinical cardiac involvement in myotonic dystrophy manifesting as decreased myocardial Doppler velocities. Neuromuscul Disord 14 (2004) 188-194
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 188-194
-
-
Vinereanu, D.1
Bajaj, B.P.2
Fenton-May, J.3
Rogers, M.T.4
Madler, C.F.5
Fraser, A.G.6
-
24
-
-
0032735294
-
Cardiomyopathy in Duchenne, Becker, and sarcoglycanopathies: a role for coronary dysfunction?
-
Gnecchi-Ruscone T., Taylor J., Mercuri E., et al. Cardiomyopathy in Duchenne, Becker, and sarcoglycanopathies: a role for coronary dysfunction?. Muscle Nerve 22 (1999) 1549-1556
-
(1999)
Muscle Nerve
, vol.22
, pp. 1549-1556
-
-
Gnecchi-Ruscone, T.1
Taylor, J.2
Mercuri, E.3
-
25
-
-
0034959387
-
Left ventricular hypertrabeculation in myotonic dystrophy type 1
-
Finsterer J., Stöllberger C., Jarius C., Wegmann R., and Janssen B. Left ventricular hypertrabeculation in myotonic dystrophy type 1. Herz 26 (2001) 287-290
-
(2001)
Herz
, vol.26
, pp. 287-290
-
-
Finsterer, J.1
Stöllberger, C.2
Jarius, C.3
Wegmann, R.4
Janssen, B.5
-
26
-
-
0347090625
-
Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data
-
Di Leo R., Rodolico C., De Gregorio C., et al. Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data. Neuromuscul Disord 14 (2004) 136-141
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 136-141
-
-
Di Leo, R.1
Rodolico, C.2
De Gregorio, C.3
-
27
-
-
0034821285
-
Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy?
-
Clarke N.R., Kelion A.D., Nixon J., Hilton-Jones D., and Forfar J.C. Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy?. Heart 86 (2001) 411-416
-
(2001)
Heart
, vol.86
, pp. 411-416
-
-
Clarke, N.R.1
Kelion, A.D.2
Nixon, J.3
Hilton-Jones, D.4
Forfar, J.C.5
-
28
-
-
0036257748
-
Severity of cardiac conduction involvement and arrhythmias in myotonic dystrophy type 1 correlates with age and CTG repeat length
-
Groh W.J., Lowe M.R., and Zipes D.P. Severity of cardiac conduction involvement and arrhythmias in myotonic dystrophy type 1 correlates with age and CTG repeat length. J Cardiovasc Electrophysiol 13 (2002) 444-448
-
(2002)
J Cardiovasc Electrophysiol
, vol.13
, pp. 444-448
-
-
Groh, W.J.1
Lowe, M.R.2
Zipes, D.P.3
-
29
-
-
0035005864
-
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy
-
Finsterer J., Gharehbaghi-Schnell E., Stollberger C., Fheodoroff K., and Seiser A. Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophy. Clin Genet 59 (2001) 350-355
-
(2001)
Clin Genet
, vol.59
, pp. 350-355
-
-
Finsterer, J.1
Gharehbaghi-Schnell, E.2
Stollberger, C.3
Fheodoroff, K.4
Seiser, A.5
-
30
-
-
19544382873
-
Familial clustering of muscular and cardiac involvement in myotonic dystrophy type 1
-
Groh W.J., Lowe M.R., Simmons Z., Bhakta D., and Pascuzzi R.M. Familial clustering of muscular and cardiac involvement in myotonic dystrophy type 1. Muscle Nerve 31 (2005) 719-724
-
(2005)
Muscle Nerve
, vol.31
, pp. 719-724
-
-
Groh, W.J.1
Lowe, M.R.2
Simmons, Z.3
Bhakta, D.4
Pascuzzi, R.M.5
-
31
-
-
85047277416
-
Quantitative assessment of the total myocardial uptake ratio of 123I-BMIPP by using the Ishii-MacIntyre method is useful for predicting cardiac complications in patients with mitochondrial encephalomyopathy or myotonic dystrophy
-
Ohkusu Y., Takahashi N., Ishikawa T., et al. Quantitative assessment of the total myocardial uptake ratio of 123I-BMIPP by using the Ishii-MacIntyre method is useful for predicting cardiac complications in patients with mitochondrial encephalomyopathy or myotonic dystrophy. Nucl Med Commun 24 (2003) 183-190
-
(2003)
Nucl Med Commun
, vol.24
, pp. 183-190
-
-
Ohkusu, Y.1
Takahashi, N.2
Ishikawa, T.3
-
32
-
-
34249308570
-
-
Heinecker, R., Gonska, B-D., EKG in Praxis und Klinik. 13th ed. Stuttgart - New York: Georg Thieme Verlag, 1992. pp. 103-104 and 292-7.
-
-
-
-
33
-
-
26444558655
-
Cardiac rehabilitation after heart transplantation in a patient with Becker's muscular dystrophy: a case report
-
Srinivasan R., Hornyak J.E., Badenhop D.T., and Koch L.G. Cardiac rehabilitation after heart transplantation in a patient with Becker's muscular dystrophy: a case report. Arch Phys Med Rehabil 86 (2005) 2059-2061
-
(2005)
Arch Phys Med Rehabil
, vol.86
, pp. 2059-2061
-
-
Srinivasan, R.1
Hornyak, J.E.2
Badenhop, D.T.3
Koch, L.G.4
-
34
-
-
22044435239
-
Midwall myocardial fibrosis in Becker-Kiener muscular dystrophy
-
Suselbeck T., Haghi D., Neff W., Borggrefe M., and Papavassiliu T. Midwall myocardial fibrosis in Becker-Kiener muscular dystrophy. Z Kardiol 94 (2005) 465-468
-
(2005)
Z Kardiol
, vol.94
, pp. 465-468
-
-
Suselbeck, T.1
Haghi, D.2
Neff, W.3
Borggrefe, M.4
Papavassiliu, T.5
-
35
-
-
0033004078
-
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy
-
Hoogerwaard E.M., van der Wouw P.A., Wilde A.A., et al. Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy. Neuromuscul Disord 9 (1999) 347-351
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 347-351
-
-
Hoogerwaard, E.M.1
van der Wouw, P.A.2
Wilde, A.A.3
-
36
-
-
0032718905
-
Cardiac involvement in Becker's muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvement
-
Finsterer J., Bittner R.E., and Grimm M. Cardiac involvement in Becker's muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvement. Neuromuscul Disord 9 (1999) 598-600
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 598-600
-
-
Finsterer, J.1
Bittner, R.E.2
Grimm, M.3
-
37
-
-
0027265702
-
Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy
-
Muntoni F., Cau M., Ganau A., et al. Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy. N Engl J Med 329 (1993) 921-925
-
(1993)
N Engl J Med
, vol.329
, pp. 921-925
-
-
Muntoni, F.1
Cau, M.2
Ganau, A.3
-
38
-
-
0037306124
-
Cardiac assessment in childhood carriers of Duchenne and Becker muscular dystrophies
-
Nolan M.A., Jones O.D., Pedersen R.L., and Johnston H.M. Cardiac assessment in childhood carriers of Duchenne and Becker muscular dystrophies. Neuromuscul Disord 13 (2003) 129-132
-
(2003)
Neuromuscul Disord
, vol.13
, pp. 129-132
-
-
Nolan, M.A.1
Jones, O.D.2
Pedersen, R.L.3
Johnston, H.M.4
-
39
-
-
17844377334
-
Echocardiographic and electrocardiographic findings of cardiomyopathy in Duchenne and Becker-Kiener muscular dystrophies
-
Kirchmann C., Kececioglu D., Korinthenberg R., and Dittrich S. Echocardiographic and electrocardiographic findings of cardiomyopathy in Duchenne and Becker-Kiener muscular dystrophies. Pediatr Cardiol 26 (2005) 66-72
-
(2005)
Pediatr Cardiol
, vol.26
, pp. 66-72
-
-
Kirchmann, C.1
Kececioglu, D.2
Korinthenberg, R.3
Dittrich, S.4
-
40
-
-
0034669478
-
Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy
-
Crilley J.G., Boehm E.A., Rajagopalan B., et al. Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy. J Am Coll Cardiol 36 (2000) 1953-1958
-
(2000)
J Am Coll Cardiol
, vol.36
, pp. 1953-1958
-
-
Crilley, J.G.1
Boehm, E.A.2
Rajagopalan, B.3
-
41
-
-
6044272949
-
Clinical presentations of mitochondrial cardiomyopathies
-
Lev D., Nissenkorn A., Leshinsky-Silver E., et al. Clinical presentations of mitochondrial cardiomyopathies. Pediatr Cardiol 25 (2004) 443-450
-
(2004)
Pediatr Cardiol
, vol.25
, pp. 443-450
-
-
Lev, D.1
Nissenkorn, A.2
Leshinsky-Silver, E.3
-
42
-
-
0242609815
-
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
-
Crimi M., Del Bo R., Galbiati S., et al. Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion. Eur J Hum Genet 11 (2003) 896-898
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 896-898
-
-
Crimi, M.1
Del Bo, R.2
Galbiati, S.3
-
43
-
-
2142649184
-
Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome
-
Ruppert V., Nolte D., Aschenbrenner T., Pankuweit S., Funck R., and Maisch B. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome. Biochem Biophys Res Commun 318 (2004) 535-543
-
(2004)
Biochem Biophys Res Commun
, vol.318
, pp. 535-543
-
-
Ruppert, V.1
Nolte, D.2
Aschenbrenner, T.3
Pankuweit, S.4
Funck, R.5
Maisch, B.6
-
44
-
-
0033981680
-
Mitochondrial defects in cardiomyopathy and neuromuscular disease
-
Wallace D.C. Mitochondrial defects in cardiomyopathy and neuromuscular disease. Am Heart J 139 (2000) 70-85
-
(2000)
Am Heart J
, vol.139
, pp. 70-85
-
-
Wallace, D.C.1
-
45
-
-
0036132663
-
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation
-
Santorelli F.M., Gagliardi M.G., Dionisi-Vici C., et al. Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation. Neuromuscul Disord 12 (2002) 56-59
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 56-59
-
-
Santorelli, F.M.1
Gagliardi, M.G.2
Dionisi-Vici, C.3
-
46
-
-
14244259670
-
Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease
-
Scaglia F., Towbin J.A., Craigen W.J., et al. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. Pediatrics 114 (2004) 925-931
-
(2004)
Pediatrics
, vol.114
, pp. 925-931
-
-
Scaglia, F.1
Towbin, J.A.2
Craigen, W.J.3
-
47
-
-
0034998813
-
Wolff-Parkinson-White syndrome and isolated left ventricular trabeculation as a manifestation of Leber's hereditary optic neuropathy
-
Finsterer J., Stöllberger C., Kopsa W., and Jaksch M. Wolff-Parkinson-White syndrome and isolated left ventricular trabeculation as a manifestation of Leber's hereditary optic neuropathy. Can J Cardiol 17 (2001) 464-466
-
(2001)
Can J Cardiol
, vol.17
, pp. 464-466
-
-
Finsterer, J.1
Stöllberger, C.2
Kopsa, W.3
Jaksch, M.4
-
48
-
-
34249276784
-
-
Finsterer J, Stöllberger C, Blazek G. Neuromuscular implications in left ventricular hypertrabeculation/noncompaction. Int J Cardiol (in press).
-
-
-
-
49
-
-
18244413442
-
Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy
-
Arbustini E., Diegoli M., Fasani R., et al. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy. Am J Pathol 153 (1998) 1501-1510
-
(1998)
Am J Pathol
, vol.153
, pp. 1501-1510
-
-
Arbustini, E.1
Diegoli, M.2
Fasani, R.3
-
50
-
-
5644291815
-
Acquired left ventricular hypertrabeculation/noncompaction in mitochondriopathy
-
Finsterer J., Stollberger C., and Schubert B. Acquired left ventricular hypertrabeculation/noncompaction in mitochondriopathy. Cardiology 102 (2004) 228-230
-
(2004)
Cardiology
, vol.102
, pp. 228-230
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Finsterer, J.1
Stollberger, C.2
Schubert, B.3
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