-
1
-
-
84891708821
-
Executive summary: Hrs/ehra/aphrs expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes
-
Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C et al. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace 2013;15: 1389-1406.
-
(2013)
Europace
, vol.15
, pp. 1389-1406
-
-
Priori, S.G.1
Wilde, A.A.2
Horie, M.3
Cho, Y.4
Behr, E.R.5
Berul, C.6
-
2
-
-
0021839929
-
Sudden unexpected death in children and adolescents
-
Driscoll DJ, Edwards WD. Sudden unexpected death in children and adolescents. J Am Coll Cardiol 1985;5:118B-121B.
-
(1985)
J Am Coll Cardiol
, vol.5
, pp. 118B-121B
-
-
Driscoll, D.J.1
Edwards, W.D.2
-
3
-
-
72449157510
-
Sudden death in persons younger than 40 years of age: Incidence and causes
-
Vaartjes I, Hendrix A, Hertogh EM, Grobbee DE, Doevendans PA, Mosterd A et al. Sudden death in persons younger than 40 years of age: incidence and causes. Eur J Cardiovasc Prev Rehabil 2009;16:592-596.
-
(2009)
Eur J Cardiovasc Prev Rehabil
, vol.16
, pp. 592-596
-
-
Vaartjes, I.1
Hendrix, A.2
Hertogh, E.M.3
Grobbee, D.E.4
Doevendans, P.A.5
Mosterd, A.6
-
4
-
-
70349501483
-
The magnitude of sudden cardiac death in the young: A death certificate-based reviewin england and wales
-
Papadakis M, Sharma S, Cox S, Sheppard MN, Panoulas VF, Behr ER. The magnitude of sudden cardiac death in the young: a death certificate-based reviewin England and Wales. Europace 2009;11:1353-1358.
-
(2009)
Europace
, vol.11
, pp. 1353-1358
-
-
Papadakis, M.1
Sharma, S.2
Cox, S.3
Sheppard, M.N.4
Panoulas, V.F.5
Behr, E.R.6
-
5
-
-
79954495564
-
Nationwide study of sudden cardiac death in persons aged 1-35 years
-
Winkel BG, Holst AG, Theilade J, Kristensen IB, Thomsen JL, Ottesen GL 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
Kristensen, I.B.4
Thomsen, J.L.5
Ottesen, G.L.6
-
6
-
-
0842330519
-
Causes of sudden cardiac death in young australians
-
Doolan A, Langlois N, Semsarian C. Causes of sudden cardiac death in young Australians. Med J Aust 2004;180:110-112.
-
(2004)
Med J Aust
, vol.180
, pp. 110-112
-
-
Doolan, A.1
Langlois, N.2
Semsarian, C.3
-
7
-
-
30344476135
-
Sudden death in the young
-
Puranik R, Chow CK, Duflou JA, Kilborn MJ, McGuire MA. Sudden death in the young. Heart Rhythm 2005;2:1277-1282.
-
(2005)
Heart Rhythm
, vol.2
, pp. 1277-1282
-
-
Puranik, R.1
Chow, C.K.2
Duflou, J.A.3
Kilborn, M.J.4
McGuire, M.A.5
-
10
-
-
84898746094
-
Sudden cardiac death in children (1-18 years): Symptoms and causes of death in a nationwide setting
-
Winkel BG, Risgaard B, Sadjadieh G, Bundgaard H, Haunsø S, Tfelt-Hansen J. Sudden cardiac death in children (1-18 years): symptoms and causes of death in a nationwide setting. Eur Heart J 2013; doi:10.1093/eurheartj/eht509.
-
(2013)
Eur Heart J
-
-
Winkel, B.G.1
Risgaard, B.2
Sadjadieh, G.3
Bundgaard, H.4
Haunsø, S.5
Tfelt-Hansen, J.6
-
11
-
-
84928335669
-
-
Unexplained deaths in infancy: England and Wales, (6 August 2012
-
Unexplained deaths in infancy: England and Wales, 2009. Office for National Statistics, 2011. http://www.ons.gov.uk/ons/dcp171778-227450.pdf (6 August 2012
-
(2009)
Office for National Statistics
, vol.2011
-
-
-
12
-
-
80055089696
-
Infant mortality statistics from the 2008 period linked birth/infant death data set
-
Hyattsville, MD National Center for Health Statistics, (6 August 2012
-
Mathews TJ, MacDormanMF. Infant Mortality Statistics from the 2008 Period Linked Birth/Infant Death Data Set. National Vital Statistics Reports; vol 60 no 5. Hyattsville, MD: National Center for Health Statistics, 2011. http://www.cdc.gov/nchs/data/nvsr/nvsr60/nvsr60-05.pdf (6 August 2012
-
(2011)
National Vital Statistics Reports
, vol.60
, Issue.5
-
-
Mathews, T.J.1
Macdorman, M.F.2
-
14
-
-
37549007151
-
Association for european cardiovascular pathology guidelines for autopsy investigation of sudden cardiac death
-
Basso C, Burke M, Fornes P, Gallagher PJ, de Gouveia RH, Sheppard M et al.; Association for European Cardiovascular Pathology. Guidelines for autopsy investigation of sudden cardiac death. Virchows Arch 2008;452:11-18.
-
(2008)
Virchows Arch
, vol.452
, pp. 11-18
-
-
Basso, C.1
Burke, M.2
Fornes, P.3
Gallagher, P.J.4
De Gouveia, R.H.5
Sheppard, M.6
-
15
-
-
84901819098
-
The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths
-
de Noronha SV, Behr ER, Papadakis M, Ohta-Ogo K, BanyaW,Wells J et al. The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths. Europace 2014;16:899-907.
-
(2014)
Europace
, vol.16
, pp. 899-907
-
-
De Noronha, S.V.1
Behr, E.R.2
Papadakis, M.3
Ohta-Ogo, K.4
Banyawwells, J.5
-
16
-
-
84884472746
-
Sudden cardiac death with autopsy findings of uncertain significance: Potential for erroneous interpretation
-
Papadakis M, Raju H, Behr ER, De Noronha SV, Spath N, Kouloubinis A et al. Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation. Circ Arrhythm Electrophysiol 2013;6:588-596.
-
(2013)
Circ Arrhythm Electrophysiol
, vol.6
, pp. 588-596
-
-
Papadakis, M.1
Raju, H.2
Behr, E.R.3
De Noronha, S.V.4
Spath, N.5
Kouloubinis, A.6
-
17
-
-
39049156814
-
Virtual autopsy using imaging: Bridging radiologic and forensic sciences a review of the virtopsy and similar projects
-
Bolliger SA, Thali MJ, Ross S, Buck U, Naether S, Vock P. Virtual autopsy using imaging: bridging radiologic and forensic sciences. A review of the virtopsy and similar projects. Eur Radiol 2008;18:273-282.
-
(2008)
Eur Radiol
, vol.18
, pp. 273-282
-
-
Bolliger, S.A.1
Thali, M.J.2
Ross, S.3
Buck, U.4
Naether, S.5
Vock, P.6
-
18
-
-
84927789131
-
Cardiovascular magnetization transfer ratio imaging compared with histology: A postmortem study
-
Crooijmans HJ, Ruder TD, Zech WD, Somaini S, Scheffler K, Thali MJ et al. Cardiovascular magnetization transfer ratio imaging compared with histology: a postmortem study. J Magn Reson Imaging 2013. .
-
(2013)
J Magn Reson Imaging
-
-
Crooijmans, H.J.1
Ruder, T.D.2
Zech, W.D.3
Somaini, S.4
Scheffler, K.5
Thali, M.J.6
-
19
-
-
84897647088
-
Ct-guided, minimally invasive, postmortem needle biopsy using the b-rob ii needlepositioning robot
-
Martinez RM, Ptacek W, Schweitzer W, Kronreif G, Fürst M, Thali MJ et al. CT-guided, minimally invasive, postmortem needle biopsy using the B-Rob II needlepositioning robot. J Forensic Sci 2013. .
-
(2013)
J Forensic Sci
-
-
Martinez, R.M.1
Ptacek, W.2
Schweitzer, W.3
Kronreif, G.4
Fürst, M.5
Thali, M.J.6
-
20
-
-
0242329842
-
Cardiological assessment of firstdegree relatives in sudden arrhythmic death syndrome
-
Sudden Arrhythmic Death Syndrome Steering Group
-
Behr E, Wood DA, Wright M, Syrris P, Sheppard MN, Casey A et al.; Sudden Arrhythmic Death Syndrome Steering Group. Cardiological assessment of firstdegree relatives in sudden arrhythmic death syndrome. Lancet 2003;362: 1457-1459.
-
(2003)
Lancet
, vol.362
, pp. 1457-1459
-
-
Behr, E.1
Wood, D.A.2
Wright, M.3
Syrris, P.4
Sheppard, M.N.5
Casey, A.6
-
21
-
-
46849110148
-
Sudden arrhythmic death syndrome: Familial evaluation identifies inheritable heart disease in the majority of families
-
Behr ER, Dalageorgou C, Christiansen M, Syrris P, Hughes S, Tome EstebanMTet al. Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families. Eur Heart J 2008;29:1670-1680.
-
(2008)
Eur Heart J
, vol.29
, pp. 1670-1680
-
-
Behr, E.R.1
Dalageorgou, C.2
Christiansen, M.3
Syrris, P.4
Hughes, S.5
Tome Esteban, M.T.6
-
22
-
-
22144439771
-
Sudden unexplained death: Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives
-
Tan HL, HofmanN, van Langen IM, van derWalAC, Wilde AA. Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives. Circulation 2005;112:207-213.
-
(2005)
Circulation
, vol.112
, pp. 207-213
-
-
Tan, H.L.1
Hofman, N.2
Van Langen, I.M.3
Van Derwal, A.C.4
Wilde, A.A.5
-
23
-
-
77957257904
-
Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: The experience of a tertiary referral center in the netherlands
-
van derWerf C, Hofman N, Tan HL, van Dessel PF, Alders M, van derWal AC et al. Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in the Netherlands. Heart Rhythm 2010;7:1383-1389.
-
(2010)
Heart Rhythm
, vol.7
, pp. 1383-1389
-
-
Van Derwerf, C.1
Hofman, N.2
Tan, H.L.3
Van Dessel, P.F.4
Alders, M.5
Van Der Wal, A.C.6
-
24
-
-
2342440911
-
Postmortemmolecular screening in unexplained sudden death
-
Chugh SS, Senashova O,Watts A, Tran PT, Zhou Z, GongQet al. Postmortemmolecular screening in unexplained sudden death. J AmColl Cardiol 2004;43:1625-1629.
-
(2004)
J AmColl Cardiol
, vol.43
, pp. 1625-1629
-
-
Chugh, S.S.1
Senashova, O.2
Watts, A.3
Tran, P.T.4
Zhou, Z.5
Gong, Q.6
-
25
-
-
33750348298
-
Postmortemlongqt syndrome genetic testing for sudden unexplained death in the young
-
Tester DJ, Ackerman MJ. PostmortemlongQT syndrome genetic testing for sudden unexplained death in the young. J Am Coll Cardiol 2007;49:240-246.
-
(2007)
J Am Coll Cardiol
, vol.49
, pp. 240-246
-
-
Tester, D.J.1
Ackerman, M.J.2
-
26
-
-
79952146247
-
Prospective population-based long qt molecular autopsy study of post-mortem negative sudden death in 1 to 40 year olds
-
Cardiac Inherited Disease Group New Zealand
-
Skinner JR, Crawford J, SmithW, Aitken A, HeavenD, EvansCAet al.; Cardiac Inherited Disease Group New Zealand. Prospective, population-based long QT molecular autopsy study of post-mortem 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
Aitken, A.4
Heaven, D.5
Evans, C.A.6
-
27
-
-
84867742485
-
The prevalence ofmutations inkcnq1,kcnh2 andscn5ain an unselected national cohort of young sudden unexplained death cases
-
Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS et al. The prevalence ofmutations inKCNQ1,KCNH2 andSCN5Ain 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
Leren, T.P.4
Nissen, P.H.5
Olesen, M.S.6
-
28
-
-
7544230111
-
Targeted mutational analysis of the cardiac ryanodine receptor (ryr2) in sudden unexplained death: A molecular autopsy of 49 medical examiner/coroner's cases
-
Tester DJ, Spoon DB, Valdivia HH, Makielski JC, Ackerman MJ. Targeted mutational analysis of the cardiac ryanodine receptor (RyR2) in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases. Mayo Clin Proc 2004; 79:1380-1384.
-
(2004)
Mayo Clin Proc
, vol.79
, pp. 1380-1384
-
-
Tester, D.J.1
Spoon, D.B.2
Valdivia, H.H.3
Makielski, J.C.4
Ackerman, M.J.5
-
29
-
-
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 Proc 2012;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
-
30
-
-
33846046495
-
Prevalence of long-qt syndrome gene variants in sudden infant death syndrome
-
Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C et al. Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation 2007;115:361-367.
-
(2007)
Circulation
, vol.115
, pp. 361-367
-
-
Arnestad, M.1
Crotti, L.2
Rognum, T.O.3
Insolia, R.4
Pedrazzini, M.5
Ferrandi, C.6
-
31
-
-
55849115645
-
Cardiac ion channel gene mutations in sudden infant death syndrome
-
Otagiri T, Kijima K, Osawa M, Ishii K, Makita N, Matoba R et al. Cardiac ion channel gene mutations in sudden infant death syndrome. Pediatr Res 2008;64: 482-487.
-
(2008)
Pediatr Res
, vol.64
, pp. 482-487
-
-
Otagiri, T.1
Kijima, K.2
Osawa, M.3
Ishii, K.4
Makita, N.5
Matoba, R.6
-
32
-
-
67349205529
-
Contribution of long-qt syndrome genetic variants in sudden infant death syndrome
-
Millat G, Kugener B, Chevalier P, Chahine M, Huang H, MalicierDet al. Contribution of long-QT syndrome genetic variants in sudden infant death syndrome. Pediatr Cardiol 2009;30:502-509.
-
(2009)
Pediatr Cardiol
, vol.30
, pp. 502-509
-
-
Millat, G.1
Kugener, B.2
Chevalier, P.3
Chahine, M.4
Huang, H.5
Malicier, D.6
-
33
-
-
0035860984
-
Postmortem molecular analysis of scn5a defects in sudden infant death syndrome
-
Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC et al. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome. JAMA 2001;286:2264-2269.
-
(2001)
JAMA
, vol.286
, pp. 2264-2269
-
-
Ackerman, M.J.1
Siu, B.L.2
Sturner, W.Q.3
Tester, D.J.4
Valdivia, C.R.5
Makielski, J.C.6
-
34
-
-
32444436881
-
A common cardiac sodium channel variant associated with sudden infant death in african americans, scn5a s1103y
-
Plant LD, Bowers PN, Liu Q, Morgan T, Zhang T, StateMWet al. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y. J Clin Invest 2006;116:430-435.
-
(2006)
J Clin Invest
, vol.116
, pp. 430-435
-
-
Plant, L.D.1
Bowers, P.N.2
Liu, Q.3
Morgan, T.4
Zhang, T.5
State, M.W.6
-
35
-
-
33846510967
-
Novel mechanism for sudden infant death syndrome: Persistent late sodium current secondary to mutations in caveolin-3
-
Cronk LB, Ye B, Kaku T, Tester DJ, Vatta M, Makielski JC et al. Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3. Heart Rhythm 2007;4:161-166.
-
(2007)
Heart Rhythm
, vol.4
, pp. 161-166
-
-
Cronk, L.B.1
Ye, B.2
Kaku, T.3
Tester, D.J.4
Vatta, M.5
Makielski, J.C.6
-
36
-
-
77952552172
-
Sudden infant death syndrome-Associated mutations in the sodium channel beta subunits
-
Tan B-H, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A et al. Sudden infant death syndrome-Associated mutations in the sodium channel beta subunits. Heart Rhythm 2010;7:771-778.
-
(2010)
Heart Rhythm
, vol.7
, pp. 771-778
-
-
Tan, B.-H.1
Pundi, K.N.2
Van Norstrand, D.W.3
Valdivia, C.R.4
Tester, D.J.5
Medeiros-Domingo, A.6
-
37
-
-
73949159312
-
Alpha1-syntrophinmutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current
-
Cheng J, VanNorstrandDW,Medeiros-Domingo A, Valdivia C, Tan BH, Ye B et al. Alpha1-syntrophinmutations Identified in sudden infant death syndrome cause an increase in late cardiac sodium current. Circ Arrhythm Electrophysiol 2009;2: 667-676.
-
(2009)
Circ Arrhythm Electrophysiol
, vol.2
, pp. 667-676
-
-
Cheng, J.1
Vannorstrand, D.W.2
Medeiros-Domingo, A.3
Valdivia, C.4
Tan, B.H.5
Ye, B.6
-
38
-
-
34147146134
-
A mechanism for sudden infant death syndrome (sids): Stress-induced leak via ryanodine receptors
-
Tester DJ, Dura M, Carturan E, Reiken S, Wronska A, Marks AR et al. A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors. Heart Rhythm 2007;4:733-739.
-
(2007)
Heart Rhythm
, vol.4
, pp. 733-739
-
-
Tester, D.J.1
Dura, M.2
Carturan, E.3
Reiken, S.4
Wronska, A.5
Marks, A.R.6
-
39
-
-
36048965546
-
Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1-like gene (gpd1-l) mutations in sudden infant death syndrome
-
Van Norstrand DW, Valdivia CR, Tester DJ, Ueda K, London B, Makielski JC et al. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) mutations in sudden infant death syndrome. Circulation 2007;116:2253-2259.
-
(2007)
Circulation
, vol.116
, pp. 2253-2259
-
-
Van Norstrand, D.W.1
Valdivia, C.R.2
Tester, D.J.3
Ueda, K.4
London, B.5
Makielski, J.C.6
-
40
-
-
82955173743
-
Loss-of-function mutations in the kcnj8-encoded kir6.1 katp channel and sudden infant death syndrome
-
Tester DJ, Tan B-H, Medeiros-Domingo A, Song C, Makielski JC, Ackerman MJ. Loss-of-function mutations in the KCNJ8-encoded Kir6.1 KATP channel and sudden infant death syndrome. Circ Cardiovasc Genet 2011;4:510-515.
-
(2011)
Circ Cardiovasc Genet
, vol.4
, pp. 510-515
-
-
Tester, D.J.1
Tan, B.-H.2
Medeiros-Domingo, A.3
Song, C.4
Makielski, J.C.5
Ackerman, M.J.6
-
41
-
-
85027941134
-
Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death
-
Van NorstrandDW, Asimaki A, Rubinos C, Dolmatova E, Srinivas M, Tester DJ et al. Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death. Circulation 2012;125:474-481.
-
(2012)
Circulation
, vol.125
, pp. 474-481
-
-
Van Norstrand, D.W.1
Asimaki, A.2
Rubinos, C.3
Dolmatova, E.4
Srinivas, M.5
Tester, D.J.6
-
42
-
-
84861577198
-
Sarcomeric gene mutations in sudden infant death syndrome (sids
-
Brion M, Allegue C, Santori M, Gil R, Blanco-Verea A, Haas C 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
Gil, R.4
Blanco-Verea, A.5
Haas, C.6
-
43
-
-
0028226701
-
A perspective on neuropathologic findings in victims of the sudden infant death syndrome: The triple-risk model
-
Filiano JJ, Kinney HC. A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model. Biol Neonate 1994;65: 194-197.
-
(1994)
Biol Neonate
, vol.65
, pp. 194-197
-
-
Filiano, J.J.1
Kinney, H.C.2
-
44
-
-
70449367296
-
Prevalence of the congenital long-qt syndrome
-
Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G et al. Prevalence of the congenital long-QT syndrome. Circulation 2009;120: 1761-1767.
-
(2009)
Circulation
, vol.120
, pp. 1761-1767
-
-
Schwartz, P.J.1
Stramba-Badiale, M.2
Crotti, L.3
Pedrazzini, M.4
Besana, A.5
Bosi, G.6
-
46
-
-
1942534554
-
Compound mutations: A common cause of severe long-qt syndrome
-
Westenskow P, Splawski I, Timothy KW, Keating MT, Sanguinetti MC. Compound mutations: a common cause of severe long-QT syndrome. Circulation 2004;109: 1834-1841.
-
(2004)
Circulation
, vol.109
, pp. 1834-1841
-
-
Westenskow, P.1
Splawski, I.2
Timothy, K.W.3
Keating, M.T.4
Sanguinetti, M.C.5
-
47
-
-
17144450747
-
Giorgetti ret al. Prolongation of the qt interval and the sudden infant death syndrome
-
Schwartz PJ, Stramba-Badiale M, Segantini A, Austoni P, Bosi G, Giorgetti Ret al. Prolongation of the QT interval and the sudden infant death syndrome. N Engl J Med 1998;338:1709-1714.
-
(1998)
N Engl J Med
, vol.338
, pp. 1709-1714
-
-
Schwartz, P.J.1
Stramba-Badiale, M.2
Segantini, A.3
Austoni, P.4
Bosi, G.5
-
48
-
-
0034721235
-
Amolecular link between the sudden infant death syndrome and the long-qt syndrome
-
Schwartz PJ, Priori SG, Dumaine R, Napolitano C, Antzelevitch C, Stramba-BadialeMet al.Amolecular link between the sudden infant death syndrome and the long-QT syndrome. N Engl J Med 2000;343:262-267.
-
(2000)
N Engl J Med
, vol.343
, pp. 262-267
-
-
Schwartz, P.J.1
Priori, S.G.2
Dumaine, R.3
Napolitano, C.4
Antzelevitch, C.5
Stramba-Badiale, M.6
-
49
-
-
22544474319
-
Sudden infant death syndrome: How significant are the channelopathies?
-
Tester DJ, Ackerman MJ. Sudden infant death syndrome: how significant are the channelopathies? Cardiovasc Res 2005;67:388-396.
-
(2005)
Cardiovasc Res
, vol.67
, pp. 388-396
-
-
Tester, D.J.1
Ackerman, M.J.2
-
50
-
-
84875210476
-
Catecholaminergic polymorphic ventricular tachycardia: From bench to bedside
-
van derWerf C, Wilde AA. Catecholaminergic polymorphic ventricular tachycardia: from bench to bedside. Heart 2013;99:497-504.
-
(2013)
Heart
, vol.99
, pp. 497-504
-
-
Van Derwerf, C.1
Wilde, A.A.2
-
51
-
-
84861719157
-
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human
-
Roux-Buisson N, Cacheux M, Fourest-Lieuvin A, Fauconnier J, Brocard J, Denjoy I et al. Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human. Hum Mol Genet 2012;21: 2759-2767.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 2759-2767
-
-
Roux-Buisson, N.1
Cacheux, M.2
Fourest-Lieuvin, A.3
Fauconnier, J.4
Brocard, J.5
Denjoy, I.6
-
52
-
-
84867242998
-
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death
-
Nyegaard M, Overgaard MT, Søndergaard MT, Vranas M, Behr ER, Hildebrandt LL et al. Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death. Am J Hum Genet 2012;91:703-712.
-
(2012)
Am J Hum Genet
, vol.91
, pp. 703-712
-
-
Nyegaard, M.1
Overgaard, M.T.2
Søndergaard, M.T.3
Vranas, M.4
Behr, E.R.5
Hildebrandt, L.L.6
-
53
-
-
13844297632
-
Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a g14876a ryanodine receptor gene mutation
-
AllouisM, Probst V, Jaafar P, Schott JJ, Le Marec H. Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation. Am J Cardiol 2005;95:700-702.
-
(2005)
Am J Cardiol
, vol.95
, pp. 700-702
-
-
Allouis, M.1
Probst, V.2
Jaafar, P.3
Schott, J.J.4
Le Marec, H.5
-
54
-
-
0017264676
-
Cardiac sympathetic innervation and the sudden infant death syndrome: A possible pathogenic link
-
Schwartz PJ. Cardiac sympathetic innervation and the sudden infant death syndrome: a possible pathogenic link. Am J Med 1976;60:167-172.
-
(1976)
Am J Med
, vol.60
, pp. 167-172
-
-
Schwartz, P.J.1
-
55
-
-
13444300924
-
Brugada syndrome: Report of the second consensus conference
-
Antzelevich C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D et al. Brugada syndrome: report of the second consensus conference. Circulation 2005; 111:659-670.
-
(2005)
Circulation
, vol.111
, pp. 659-670
-
-
Antzelevich, C.1
Brugada, P.2
Borggrefe, M.3
Brugada, J.4
Brugada, R.5
Corrado, D.6
-
56
-
-
84870570379
-
Brugada syndrome: Two decades of progress
-
Veerakul G, Nademanee K. Brugada syndrome: two decades of progress. Circ J 2012; 76:2713-2722.
-
(2012)
Circ J
, vol.76
, pp. 2713-2722
-
-
Veerakul, G.1
Nademanee, K.2
-
57
-
-
79957988353
-
Low prevalence of risk markers in cases of sudden death due to brugada syndrome relevance to risk stratification in brugada syndrome
-
Raju H, Papadakis M, Govindan M, Bastiaenen R, Chandra N, O'Sullivan A et al. Low prevalence of risk markers in cases of sudden death due to Brugada syndrome relevance to risk stratification in Brugada syndrome. J Am Coll Cardiol 2011;57: 2340-2345.
-
(2011)
J Am Coll Cardiol
, vol.57
, pp. 2340-2345
-
-
Raju, H.1
Papadakis, M.2
Govindan, M.3
Bastiaenen, R.4
Chandra, N.5
O'Sullivan, A.6
-
58
-
-
18244408818
-
Near-miss sids due to brugada syndrome
-
Skinner JR, Chung S-K, Montgomery D, McCulley CH, Crawford J, French J et al. Near-miss SIDS due to Brugada syndrome. Arch Dis Child 2005;90:528-529.
-
(2005)
Arch Dis Child
, vol.90
, pp. 528-529
-
-
Skinner, J.R.1
Chung, S.-K.2
Montgomery, D.3
McCulley, C.H.4
Crawford, J.5
French, J.6
-
59
-
-
49349104847
-
Heterozygous nonsense scn5a mutation w822x explains a simultaneous sudden infant death syndrome
-
Turillazzi E, La Rocca G, Anzalone R, CorraoS, Neri M, PomaraCet al. Heterozygous nonsense SCN5A mutation W822X explains a simultaneous sudden infant death syndrome. Virchows Arch 2008;453:209-216.
-
(2008)
Virchows Arch
, vol.453
, pp. 209-216
-
-
Turillazzi, E.1
La Rocca, G.2
Anzalone, R.3
Corrao, S.4
Neri, M.5
Pomara, C.6
-
60
-
-
84859978568
-
A novel rare variant in scn1bb linked to brugada syndrome and sids by combined modulation of na(v)1.5 and k(v)4.3 channel currents
-
Hu D, Barajas-Martinez H, Medeiros-Domingo A, Crotti L, Veltmann C, Schimpf R et al. A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents. Heart Rhythm 2012;9: 760-769.
-
(2012)
Heart Rhythm
, vol.9
, pp. 760-769
-
-
Hu, D.1
Barajas-Martinez, H.2
Medeiros-Domingo, A.3
Crotti, L.4
Veltmann, C.5
Schimpf, R.6
-
61
-
-
84855406346
-
Brugadalike syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay
-
Kanter RJ, PfeifferR,HuD, Barajas-Martinez H, CarboniMP, Antzelevich C. Brugadalike syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay. Circulation 2012;125:14-22.
-
(2012)
Circulation
, vol.125
, pp. 14-22
-
-
Kanter, R.J.1
Pfeiffer, R.2
Hu, D.3
Barajas-Martinez, H.4
Carboni, M.P.5
Antzelevich, C.6
-
62
-
-
77953680594
-
A common single nucleotide polymorphism can exacerbate long-qt type 2 syndrome leading to sudden infant death
-
Nof E, Cordeiro JM, Pérez GJ, Scornik FS, Calloe K, Love B et al. A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death. Circ Cardiovasc Genet 2010;3:199-206.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 199-206
-
-
Nof, E.1
Cordeiro, J.M.2
Pérez, G.J.3
Scornik, F.S.4
Calloe, K.5
Love, B.6
-
63
-
-
23844527207
-
Role of scn5a y1102 polymorphism in sudden cardiac death in blacks
-
Burke A, Creighton W, Mont E, Li L, Hogan S, Kutys R et al. Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks. Circulation 2005;112: 798-802.
-
(2005)
Circulation
, vol.112
, pp. 798-802
-
-
Burke, A.1
Creighton, W.2
Mont, E.3
Li, L.4
Hogan, S.5
Kutys, R.6
-
64
-
-
33846425740
-
Cardiac sodium channel dysfunction in sudden infant death syndrome
-
Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M et al. Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation 2007; 115:368-376.
-
(2007)
Circulation
, vol.115
, pp. 368-376
-
-
Wang, D.W.1
Desai, R.R.2
Crotti, L.3
Arnestad, M.4
Insolia, R.5
Pedrazzini, M.6
-
65
-
-
84555222948
-
Double or compound sarcomere mutations in hypertrophic cardiomyopathy: A potential link to sudden death in the absence of conventional risk factors
-
Maron BJ, Maron MS, Semsarian C. Double or compound sarcomere mutations in hypertrophic cardiomyopathy: a potential link to sudden death in the absence of conventional risk factors. Heart Rhythm 2012;9:57-63.
-
(2012)
Heart Rhythm
, vol.9
, pp. 57-63
-
-
Maron, B.J.1
Maron, M.S.2
Semsarian, C.3
-
66
-
-
84879594311
-
Familial cardiological evaluation in sudden arrhythmic death syndrome: Essential but challenging
-
Wong LC, Behr ER. Familial cardiological evaluation in sudden arrhythmic death syndrome: essential but challenging. Europace 2013;15:924-926.
-
(2013)
Europace
, vol.15
, pp. 924-926
-
-
Wong, L.C.1
Behr, E.R.2
-
67
-
-
84879578013
-
Familybased cardiac screening in relatives of victims of sudden arrhythmic death syndrome
-
McGorrian C, Constant O, Harper N, O'Donnell C, Codd M, Keelan E et al. Familybased cardiac screening in relatives of victims of sudden arrhythmic death syndrome. Europace 2013;15:1050-1058.
-
(2013)
Europace
, vol.15
, pp. 1050-1058
-
-
McGorrian, C.1
Constant, O.2
Harper, N.3
O'Donnell, C.4
Codd, M.5
Keelan, E.6
-
68
-
-
79952180945
-
Sudden cardiac death: Clinical evaluation of paediatric family members
-
Tomaske M, Keller DI, Bauersfeld U. Sudden cardiac death: clinical evaluation of paediatric family members. Europace 2011;13:421-426.
-
(2011)
Europace
, vol.13
, pp. 421-426
-
-
Tomaske, M.1
Keller, D.I.2
Bauersfeld, U.3
-
69
-
-
84885022072
-
Yield of molecular and clinical testing for arrhythmia syndromes: Report of 15 years' experience
-
Hofman N, Tan HL, AldersM, Kolder I, de Haij S, MannensMMet al. Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience. Circulation 2013;128:1513-1521.
-
(2013)
Circulation
, vol.128
, pp. 1513-1521
-
-
Hofman, N.1
Tan, H.L.2
Alders, M.3
Kolder, I.4
De Haij, S.5
Mannens, M.M.6
-
70
-
-
35148819135
-
Contribution of inherited heart disease to sudden cardiac death in childhood
-
HofmanN, Tan HL, Clur S-A, Alders M, van Langen IM, WildeAAM. Contribution of inherited heart disease to sudden cardiac death in childhood. Pediatrics 2007;120: e967-e973.
-
(2007)
Pediatrics
, vol.120
, pp. e967-e973
-
-
Hofman, N.1
Tan, H.L.2
Clur, S.-A.3
Alders, M.4
Van Langen, I.M.5
Wilde, A.A.M.6
-
71
-
-
80051710052
-
Heart rhythm society (hrs); European heart rhythm association (ehra hrs/ehra expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies
-
Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H et al.; Heart Rhythm Society (HRS); European Heart Rhythm Association (EHRA). HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies. Europace 2011;13:1077-1109.
-
(2011)
Europace
, vol.13
, pp. 1077-1109
-
-
Ackerman, M.J.1
Priori, S.G.2
Willems, S.3
Berul, C.4
Brugada, R.5
Calkins, H.6
-
72
-
-
70349338813
-
Yield of genetic screening in inherited cardiac channelopathies: How to prioritize access to genetic testing
-
Bai R, Napolitano C, Bloise R, Monteforte N, Priori SG. Yield of genetic screening in inherited cardiac channelopathies: how to prioritize access to genetic testing. Circ Arrhythm Electrophysiol 2009;2:6-15.
-
(2009)
Circ Arrhythm Electrophysiol
, vol.2
, pp. 6-15
-
-
Bai, R.1
Napolitano, C.2
Bloise, R.3
Monteforte, N.4
Priori, S.G.5
-
73
-
-
84928343672
-
Cost-effectiveness of the molecular autopsy' in sudden unexplained death in the young
-
Ingles J, Semsarian C. Cost-effectiveness of the 'Molecular Autopsy' in sudden unexplained death in the young. Heart Lung Circ 2012;21:S266.
-
(2012)
Heart Lung Circ
, vol.21
, pp. S266
-
-
Ingles, J.1
Semsarian, C.2
-
74
-
-
84928313054
-
Cost comparison between postmortem genetic testing and first degree relative clinical testing following autopsy negative sudden unexplained death
-
Tester DJ, Medeiros-Domingo A, Haglund CM, Johnson JN, Ackerman MJ. Cost comparison between postmortem genetic testing and first degree relative clinical testing following autopsy negative sudden unexplained death. Circulation 2009;120: S566.
-
(2009)
Circulation
, vol.120
, pp. S566
-
-
Tester, D.J.1
Medeiros-Domingo, A.2
Haglund, C.M.3
Johnson, J.N.4
Ackerman, M.J.5
|