-
1
-
-
79954495564
-
Nationwide study of sudden cardiac death in persons aged 1-35 years
-
Winkel BG, Holst AG, Theilade J et al: Nationwide study of sudden cardiac death in persons aged 1-35 years. Eur Heart J 2011; 32: 983-990.
-
(2011)
Eur Heart J
, vol.32
, pp. 983-990
-
-
Winkel, B.G.1
Holst, A.G.2
Theilade, J.3
-
2
-
-
84900395460
-
Burden of sudden cardiac death in persons aged 1 to 49 years: Nationwide study in Denmark
-
Risgaard B, Winkel BG, Jabbari R et al: Burden of sudden cardiac death in persons aged 1 to 49 years: nationwide study in Denmark. Circ Arrhythm Electrophysiol 2014; 7: 205-211.
-
(2014)
Circ Arrhythm Electrophysiol
, vol.7
, pp. 205-211
-
-
Risgaard, B.1
Winkel, B.G.2
Jabbari, R.3
-
3
-
-
84896749603
-
Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype
-
Cerrone M, Lin X, Zhang M et al: Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype. Circulation 2014; 129: 1092-1103.
-
(2014)
Circulation
, vol.129
, pp. 1092-1103
-
-
Cerrone, M.1
Lin, X.2
Zhang, M.3
-
4
-
-
84255168588
-
PKP2 mutations in sudden death from arrhythmogenic right ventricular cardiomyopathy (ARVC) and sudden unexpected death with negative autopsy (SUDNA)
-
Zhang M, Tavora F, Oliveira JB et al: PKP2 mutations in sudden death from arrhythmogenic right ventricular cardiomyopathy (ARVC) and sudden unexpected death with negative autopsy (SUDNA). Circ J 2012; 76: 189-194.
-
(2012)
Circ J
, vol.76
, pp. 189-194
-
-
Zhang, M.1
Tavora, F.2
Oliveira, J.B.3
-
5
-
-
84881137449
-
Silencing of desmoplakin decreases connexin43/Nav1.5 expression and sodium current in HL1 cardiomyocytes
-
Zhang Q, Deng C, Rao F et al: Silencing of desmoplakin decreases connexin43/Nav1.5 expression and sodium current in HL1 cardiomyocytes. Mol Med Rep 2013; 8: 780-786.
-
(2013)
Mol Med Rep
, vol.8
, pp. 780-786
-
-
Zhang, Q.1
Deng, C.2
Rao, F.3
-
6
-
-
84865214658
-
Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes
-
Rizzo S, Lodder EM, Verkerk AO et al: Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes. Cardiovasc Res 2012; 95: 409-418.
-
(2012)
Cardiovasc Res
, vol.95
, pp. 409-418
-
-
Rizzo, S.1
Lodder, E.M.2
Verkerk, A.O.3
-
7
-
-
79952146247
-
Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds
-
Skinner JR, Crawford J, Smith W et al: Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds. Heart Rhythm 2011; 8: 412-419.
-
(2011)
Heart Rhythm
, vol.8
, pp. 412-419
-
-
Skinner, J.R.1
Crawford, J.2
Smith, W.3
-
8
-
-
84867742485
-
The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases
-
Winkel BG, Larsen MK, Berge KE et al: The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases. J Cardiovasc Electrophysiol 2012; 23: 1092-1098.
-
(2012)
J Cardiovasc Electrophysiol
, vol.23
, pp. 1092-1098
-
-
Winkel, B.G.1
Larsen, M.K.2
Berge, K.E.3
-
9
-
-
84863484022
-
Cardiac channel molecular autopsy: Insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing
-
Tester DJ, Medeiros-Domingo A, Will ML, Haglund CM, Ackerman MJ: Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing. Mayo Clin Proc2012; 87: 524-539.
-
(2012)
Mayo Clin Proc
, vol.87
, pp. 524-539
-
-
Tester, D.J.1
Medeiros-Domingo, A.2
Will, M.L.3
Haglund, C.M.4
Ackerman, M.J.5
-
10
-
-
84886878667
-
Genetic analysis of sudden unexplained death: A multidisciplinary approach
-
Kauferstein S, Kiehne N, Jenewein T et al: Genetic analysis of sudden unexplained death: a multidisciplinary approach. Forensic Sci Int 2013; 229: 122-127.
-
(2013)
Forensic Sci Int
, vol.229
, pp. 122-127
-
-
Kauferstein, S.1
Kiehne, N.2
Jenewein, T.3
-
11
-
-
84931575992
-
Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases
-
Hertz CL, Christiansen SL, Ferrero-Miliani L et al: Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases. Int J Legal Med 2015; 129: 793-800.
-
(2015)
Int J Legal Med
, vol.129
, pp. 793-800
-
-
Hertz, C.L.1
Christiansen, S.L.2
Ferrero-Miliani, L.3
-
12
-
-
84925501370
-
Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: A case series
-
Narula N, Tester DJ, Paulmichl A, Maleszewski JJ, Ackerman MJ: Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: a case series. Pediatr Cardiol 2015; 36: 768-778.
-
(2015)
Pediatr Cardiol
, vol.36
, pp. 768-778
-
-
Narula, N.1
Tester, D.J.2
Paulmichl, A.3
Maleszewski, J.J.4
Ackerman, M.J.5
-
13
-
-
84896921083
-
Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young
-
Bagnall RD, Das KJ, Duflou J, Semsarian C: Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young. Heart Rhythm 2014; 11: 655-662.
-
(2014)
Heart Rhythm
, vol.11
, pp. 655-662
-
-
Bagnall, R.D.1
Das, K.J.2
Duflou, J.3
Semsarian, C.4
-
14
-
-
84907267767
-
Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencing
-
Loporcaro CG, Tester DJ, Maleszewski JJ, Kruisselbrink T, Ackerman MJ: Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencing. Arch Pathol Lab Med2014; 138: 1083-1089.
-
(2014)
Arch Pathol Lab Med
, vol.138
, pp. 1083-1089
-
-
Loporcaro, C.G.1
Tester, D.J.2
Maleszewski, J.J.3
Kruisselbrink, T.4
Ackerman, M.J.5
-
15
-
-
84954391232
-
Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart
-
Hertz CL, Christiansen SL, Ferrero-Miliani L et al: Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart. Int J Legal Med 2015; 130: 91-102.
-
(2015)
Int J Legal Med
, vol.130
, pp. 91-102
-
-
Hertz, C.L.1
Christiansen, S.L.2
Ferrero-Miliani, L.3
-
16
-
-
84941242581
-
Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases
-
Hertz CL, Christiansen SL, Larsen MK et al: Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases. Eur J Hum Genet 2015; 24: 817-822.
-
(2015)
Eur J Hum Genet
, vol.24
, pp. 817-822
-
-
Hertz, C.L.1
Christiansen, S.L.2
Larsen, M.K.3
-
17
-
-
0037903275
-
Human Gene Mutation Database (HGMD) 2003 update
-
Stenson PD, Ball EV, Mort M et al: Human Gene Mutation Database (HGMD): 2003 update. Hum Mutat 2003; 21: 577-581.
-
(2003)
Hum Mutat
, vol.21
, pp. 577-581
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
-
18
-
-
84928209346
-
Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
-
Richards S, Aziz N, Bale S et al: Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015; 17: 405-423.
-
(2015)
Genet Med
, vol.17
, pp. 405-423
-
-
Richards, S.1
Aziz, N.2
Bale, S.3
-
19
-
-
84884506830
-
Interpreting secondary cardiac disease variants in an exome cohort
-
Ng D, Johnston JJ, Teer JK et al: Interpreting secondary cardiac disease variants in an exome cohort. Circ Cardiovasc Genet 2013; 6: 337-346.
-
(2013)
Circ Cardiovasc Genet
, vol.6
, pp. 337-346
-
-
Ng, D.1
Johnston, J.J.2
Teer, J.K.3
-
20
-
-
84885295208
-
Actionable, pathogenic incidental findings in 1000 participants' exomes
-
Dorschner MO, Amendola LM, Turner EH et al: Actionable, pathogenic incidental findings in 1000 participants' exomes. Am J Hum Genet 2013; 93: 631-640.
-
(2013)
Am J Hum Genet
, vol.93
, pp. 631-640
-
-
Dorschner, M.O.1
Amendola, L.M.2
Turner, E.H.3
-
21
-
-
84857641821
-
Differential confounding of rare and common variants in spatially structured populations
-
Mathieson I, McVean G: Differential confounding of rare and common variants in spatially structured populations. Nat Genet 2012; 44: 243-246.
-
(2012)
Nat Genet
, vol.44
, pp. 243-246
-
-
Mathieson, I.1
McVean, G.2
-
22
-
-
84890260477
-
Whole-exome sequencing of 2000 Danish individuals and the role of rare coding variants in type 2 diabetes
-
Lohmueller KE, Sparso T, Li Q et al: Whole-exome sequencing of 2000 Danish individuals and the role of rare coding variants in type 2 diabetes. Am J Hum Genet 2013; 93: 1072-1086.
-
(2013)
Am J Hum Genet
, vol.93
, pp. 1072-1086
-
-
Lohmueller, K.E.1
Sparso, T.2
Li, Q.3
-
24
-
-
11444264507
-
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
-
Gerull B, Heuser A, Wichter T et al: Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat Genet 2004; 36: 1162-1164.
-
(2004)
Nat Genet
, vol.36
, pp. 1162-1164
-
-
Gerull, B.1
Heuser, A.2
Wichter, T.3
-
25
-
-
75449104614
-
Missense variants in plakophilin-2 in arrhythmogenic right ventricular cardiomyopathy patients- disease-causing or innocent bystanders?
-
Christensen AH, Benn M, Tybjaerg-Hansen A, Haunso S, Svendsen JH: Missense variants in plakophilin-2 in arrhythmogenic right ventricular cardiomyopathy patients- disease-causing or innocent bystanders? Cardiology 2010; 115: 148-154.
-
(2010)
Cardiology
, vol.115
, pp. 148-154
-
-
Christensen, A.H.1
Benn, M.2
Tybjaerg-Hansen, A.3
Haunso, S.4
Svendsen, J.H.5
-
26
-
-
84861577198
-
Sarcomeric gene mutations in sudden infant death syndrome (SIDS
-
Brion M, Allegue C, Santori M et al: Sarcomeric gene mutations in sudden infant death syndrome (SIDS). Forensic Sci Int 2012; 219: 278-281.
-
(2012)
Forensic Sci Int
, vol.219
, pp. 278-281
-
-
Brion, M.1
Allegue, C.2
Santori, M.3
-
27
-
-
77952536025
-
A novel custom resequencing array for dilated cardiomyopathy
-
Zimmerman RS, Cox S, Lakdawala NK et al: A novel custom resequencing array for dilated cardiomyopathy. Genet Med 2010; 12: 268-278.
-
(2010)
Genet Med
, vol.12
, pp. 268-278
-
-
Zimmerman, R.S.1
Cox, S.2
Lakdawala, N.K.3
-
28
-
-
42949149810
-
Shared genetic causes of cardiac hypertrophy in children and adults
-
Morita H, Rehm HL, Menesses A et al: Shared genetic causes of cardiac hypertrophy in children and adults. N Engl J Med 2008; 358: 1899-1908.
-
(2008)
N Engl J Med
, vol.358
, pp. 1899-1908
-
-
Morita, H.1
Rehm, H.L.2
Menesses, A.3
-
29
-
-
84882453618
-
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants
-
Andreasen C, Nielsen JB, Refsgaard L et al: New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants. Eur J Hum Genet 2013; 21: 918-928.
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 918-928
-
-
Andreasen, C.1
Nielsen, J.B.2
Refsgaard, L.3
-
30
-
-
77956445622
-
Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy
-
Roberts JD, Veinot JP, Rutberg J, Gollob MH: Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy. Cardiovasc Pathol 2010; 19: 316-320.
-
(2010)
Cardiovasc Pathol
, vol.19
, pp. 316-320
-
-
Roberts, J.D.1
Veinot, J.P.2
Rutberg, J.3
Gollob, M.H.4
-
32
-
-
84886295680
-
Postmortem analysis of cardiovascular deaths in schizophrenia: A 10-year review
-
Sweeting J, Duflou J, Semsarian C: Postmortem analysis of cardiovascular deaths in schizophrenia: a 10-year review. Schizophr Res 2013; 150: 398-403.
-
(2013)
Schizophr Res
, vol.150
, pp. 398-403
-
-
Sweeting, J.1
Duflou, J.2
Semsarian, C.3
-
33
-
-
84862590416
-
Antidepressant use and risk of out-of-hospital cardiac arrest: A nationwide case-time-control study
-
Weeke P, Jensen A, Folke F et al: Antidepressant use and risk of out-of-hospital cardiac arrest: a nationwide case-time-control study. Clin Pharmacol Ther 2012; 92: 72-79.
-
(2012)
Clin Pharmacol Ther
, vol.92
, pp. 72-79
-
-
Weeke, P.1
Jensen, A.2
Folke, F.3
-
34
-
-
84901341491
-
Risk of arrhythmia induced by psychotropic medications: A proposal for clinical management
-
Fanoe S, Kristensen D, Fink-Jensen A et al: Risk of arrhythmia induced by psychotropic medications: a proposal for clinical management. Eur Heart J 2014; 35: 1306-1315.
-
(2014)
Eur Heart J
, vol.35
, pp. 1306-1315
-
-
Fanoe, S.1
Kristensen, D.2
Fink-Jensen, A.3
-
35
-
-
3042542936
-
Antipsychotics and the risk of sudden cardiac death
-
Straus SM, Bleumink GS, Dieleman JP et al: Antipsychotics and the risk of sudden cardiac death. Arch Intern Med 2004; 164: 1293-1297.
-
(2004)
Arch Intern Med
, vol.164
, pp. 1293-1297
-
-
Straus, S.M.1
Bleumink, G.S.2
Dieleman, J.P.3
-
36
-
-
0035199932
-
Antipsychotics and the risk of sudden cardiac death
-
Ray WA, Meredith S, Thapa PB, Meador KG, Hall K, Murray KT: Antipsychotics and the risk of sudden cardiac death. Arch Gen Psychiatry 2001; 58: 1161-1167.
-
(2001)
Arch Gen Psychiatry
, vol.58
, pp. 1161-1167
-
-
Ray, W.A.1
Meredith, S.2
Thapa, P.B.3
Meador, K.G.4
Hall, K.5
Murray, K.T.6
-
37
-
-
58349114259
-
Atypical antipsychotic drugs and the risk of sudden cardiac death
-
Ray WA, Chung CP, Murray KT, Hall K, Stein CM: Atypical antipsychotic drugs and the risk of sudden cardiac death. N Engl J Med 2009; 360: 225-235.
-
(2009)
N Engl J Med
, vol.360
, pp. 225-235
-
-
Ray, W.A.1
Chung, C.P.2
Murray, K.T.3
Hall, K.4
Stein, C.M.5
-
38
-
-
0031469059
-
Sudden unexpected death in epilepsy: Terminology and definitions
-
Nashef L: Sudden unexpected death in epilepsy: terminology and definitions. Epilepsia 1997; 38(Suppl 11): S6-S8.
-
(1997)
Epilepsia
, vol.38
, pp. S6-S8
-
-
Nashef, L.1
-
39
-
-
84883744062
-
Epilepsy and risk of death and sudden unexpected death in the young: A nationwide study
-
Holst AG, Winkel BG, Risgaard B et al: Epilepsy and risk of death and sudden unexpected death in the young: a nationwide study. Epilepsia 2013; 54: 1613-1620.
-
(2013)
Epilepsia
, vol.54
, pp. 1613-1620
-
-
Holst, A.G.1
Winkel, B.G.2
Risgaard, B.3
-
40
-
-
84939874727
-
Genetic and forensic implications in epilepsy and cardiac arrhythmias: A case series
-
Partemi S, Vidal MC, Striano P et al: Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series. Int J Legal Med 2015; 129: 495-504.
-
(2015)
Int J Legal Med
, vol.129
, pp. 495-504
-
-
Partemi, S.1
Vidal, M.C.2
Striano, P.3
-
41
-
-
84940437691
-
Sudden unexpected death in epilepsy: Some approaches for its prevention and medico-legal consideration
-
Verma A, Kumar A: Sudden unexpected death in epilepsy: some approaches for its prevention and medico-legal consideration. Acta Neurol Belg 2015; 115: 207-212.
-
(2015)
Acta Neurol Belg
, vol.115
, pp. 207-212
-
-
Verma, A.1
Kumar, A.2
-
43
-
-
79251560652
-
Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases
-
Tu E, Bagnall RD, Duflou J, Semsarian C: Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases. Brain Pathol 2011; 21: 201-208.
-
(2011)
Brain Pathol
, vol.21
, pp. 201-208
-
-
Tu, E.1
Bagnall, R.D.2
Duflou, J.3
Semsarian, C.4
-
44
-
-
0033976150
-
Novel repeats in ryanodine and IP3 receptors and protein O-mannosyltransferases
-
Ponting CP: Novel repeats in ryanodine and IP3 receptors and protein O-mannosyltransferases. Trends Biochem Sci 2000; 25: 48-50.
-
(2000)
Trends Biochem Sci
, vol.25
, pp. 48-50
-
-
Ponting, C.P.1
-
45
-
-
78650088297
-
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
-
Burashnikov E, Pfeiffer R, Barajas-Martinez H et al: Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. Heart Rhythm 2010; 7: 1872-1882.
-
(2010)
Heart Rhythm
, vol.7
, pp. 1872-1882
-
-
Burashnikov, E.1
Pfeiffer, R.2
Barajas-Martinez, H.3
-
46
-
-
0032831603
-
Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects
-
Swan H, Viitasalo M, Piippo K, Laitinen P, Kontula K, Toivonen L: Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects. J Am Coll Cardiol 1999; 34: 823-829.
-
(1999)
J Am Coll Cardiol
, vol.34
, pp. 823-829
-
-
Swan, H.1
Viitasalo, M.2
Piippo, K.3
Laitinen, P.4
Kontula, K.5
Toivonen, L.6
-
47
-
-
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 2004; 44: 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
-
48
-
-
17144415220
-
Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
-
Tester DJ, Will ML, Haglund CM, Ackerman MJ: Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. Heart Rhythm 2005; 2: 507-517.
-
(2005)
Heart Rhythm
, vol.2
, pp. 507-517
-
-
Tester, D.J.1
Will, M.L.2
Haglund, C.M.3
Ackerman, M.J.4
-
49
-
-
10744231816
-
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome
-
Zareba W, Moss AJ, Sheu G et al: Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome. J Cardiovasc Electrophysiol 2003; 14: 1149-1153.
-
(2003)
J Cardiovasc Electrophysiol
, vol.14
, pp. 1149-1153
-
-
Zareba, W.1
Moss, A.J.2
Sheu, G.3
-
50
-
-
33645772930
-
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy
-
van Tintelen JP, Entius MM, Bhuiyan ZA et al: Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation 2006; 113: 1650-1658.
-
(2006)
Circulation
, vol.113
, pp. 1650-1658
-
-
Van Tintelen, J.P.1
Entius, M.M.2
Bhuiyan, Z.A.3
-
51
-
-
84904053841
-
PDZ domain-binding motif regulates cardiomyocyte compartment-specific NaV1.5 channel expression and function
-
Shy D, Gillet L, Ogrodnik J et al: PDZ domain-binding motif regulates cardiomyocyte compartment-specific NaV1.5 channel expression and function. Circulation 2014; 130: 147-160.
-
(2014)
Circulation
, vol.130
, pp. 147-160
-
-
Shy, D.1
Gillet, L.2
Ogrodnik, J.3
-
52
-
-
68949209933
-
Spectrum and prevalence of mutations from the first 2500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test
-
Kapplinger JD, Tester DJ, Salisbury BA et al: Spectrum and prevalence of mutations from the first 2500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm 2009; 6: 1297-1303.
-
(2009)
Heart Rhythm
, vol.6
, pp. 1297-1303
-
-
Kapplinger, J.D.1
Tester, D.J.2
Salisbury, B.A.3
|