-
1
-
-
0025935591
-
The long QT syndrome: Prospective longitudinal study of 328 families
-
Moss AJ, Schwartz PJ, Crampton RS, Tzivoni D, Locati EH, MacCluer J, et al. The long QT syndrome: prospective longitudinal study of 328 families. Circulation 1991;84:1136-44.
-
(1991)
Circulation
, vol.84
, pp. 1136-1144
-
-
Moss, A.J.1
Schwartz, P.J.2
Crampton, R.S.3
Tzivoni, D.4
Locati, E.H.5
MacCluer, J.6
-
2
-
-
0026759352
-
The spectrum of symptoms and QT intervals in carriers of the gene for long QT syndrome
-
Vincent GM, Timothy KM, Leppert M, Keating M. The spectrum of symptoms and QT intervals in carriers of the gene for long QT syndrome. N Engl J Med 1992;327:846-52.
-
(1992)
N Engl J Med
, vol.327
, pp. 846-852
-
-
Vincent, G.M.1
Timothy, K.M.2
Leppert, M.3
Keating, M.4
-
3
-
-
0027267765
-
Diagnostic criteria for the long QT syndrome: An update
-
Schwartz PJ, Moss AJ, Vincent GM, et al. Diagnostic criteria for the long QT syndrome: an update. Circulation 1993;88:782-4.
-
(1993)
Circulation
, vol.88
, pp. 782-784
-
-
Schwartz, P.J.1
Moss, A.J.2
Vincent, G.M.3
-
4
-
-
75549109609
-
Aritmie cardiache rare dell'eta pediatrica.
-
Romano C, Gemme G, Pongiglione R. Aritmie cardiache rare dell'eta pediatrica. Clin Pediatr 1963;45:656-83.
-
(1963)
Clin Pediatr
, vol.45
, pp. 656-683
-
-
Romano, C.1
Gemme, G.2
Pongiglione, R.3
-
5
-
-
0000387603
-
A new familial cardiac syndrome in children
-
Ward OC. A new familial cardiac syndrome in children. J Irish Med Assoc 1964;54:103-6.
-
(1964)
J Irish Med Assoc
, vol.54
, pp. 103-106
-
-
Ward, O.C.1
-
6
-
-
49749174698
-
Congenital deaf-mutism, functional heart disease with prolongation of the QT interval, and sudden death
-
Jervell A, Lange-Nielsen F. Congenital deaf-mutism, functional heart disease with prolongation of the QT interval, and sudden death. Am Heart J 1957;54:59-68.
-
(1957)
Am Heart J
, vol.54
, pp. 59-68
-
-
Jervell, A.1
Lange-Nielsen, F.2
-
7
-
-
0037217202
-
Catecholamine-induced T-wave lability in congenital long QT syndrome: A novel phenomenon associated with syncope and cardiac arrest
-
Nemec J, Hejlik JB, Shen WK, Ackerman MJ. Catecholamine-induced T-wave lability in congenital long QT syndrome: a novel phenomenon associated with syncope and cardiac arrest. Mayo Clin Proc 2003;78:40-50.
-
(2003)
Mayo Clin Proc
, vol.78
, pp. 40-50
-
-
Nemec, J.1
Hejlik, J.B.2
Shen, W.K.3
Ackerman, M.J.4
-
9
-
-
0001221406
-
Congenital deafness associated with electrocardiographic abnormalities, fainting attacks and sudden death
-
Fraser GR, Froggatt P, James TN. Congenital deafness associated with electrocardiographic abnormalities, fainting attacks and sudden death. Q J Med 1964;33:361-85.
-
(1964)
Q J Med
, vol.33
, pp. 361-385
-
-
Fraser, G.R.1
Froggatt, P.2
James, T.N.3
-
11
-
-
0038415858
-
-
Priori SG, Schwartz PJ, Napolitano C, Bloise R, Ronchetti E, Grillo M, et al. Risk stratification in the long-QT syndrome. N Engl J Med 2003;348:1866-74.
-
Priori SG, Schwartz PJ, Napolitano C, Bloise R, Ronchetti E, Grillo M, et al. Risk stratification in the long-QT syndrome. N Engl J Med 2003;348:1866-74.
-
-
-
-
12
-
-
0022870955
-
Prolonged QT interval syndromes
-
Moss AJ. Prolonged QT interval syndromes. J Am Med Assoc 1986;256:2985-7.
-
(1986)
J Am Med Assoc
, vol.256
, pp. 2985-2987
-
-
Moss, A.J.1
-
13
-
-
0031916794
-
The long QT syndrome: Ion channel diseases of the heart
-
Ackerman MJ. The long QT syndrome: ion channel diseases of the heart. Mayo Clin Proc 1998;73:250-69.
-
(1998)
Mayo Clin Proc
, vol.73
, pp. 250-269
-
-
Ackerman, M.J.1
-
14
-
-
0031978985
-
The molecular genetics of the long QT syndrome: Genes causing fainting and sudden death
-
Vincent GM. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death. Annu Rev Med 1998;49:263-74.
-
(1998)
Annu Rev Med
, vol.49
, pp. 263-274
-
-
Vincent, G.M.1
-
15
-
-
17944381537
-
Task force on sudden cardiac death of the European Society of Cardiology
-
Priori SG, Aliot E, Blomstrom-Lundquist C, Bossaert L, Breithardt G, Brugada P, et al. Task force on sudden cardiac death of the European Society of Cardiology. Eur Heart J 2001;22:1374-450.
-
(2001)
Eur Heart J
, vol.22
, pp. 1374-1450
-
-
Priori, S.G.1
Aliot, E.2
Blomstrom-Lundquist, C.3
Bossaert, L.4
Breithardt, G.5
Brugada, P.6
-
16
-
-
33644821919
-
The congenital long QT syndromes from genotype to phenotype: Clinical implications
-
Schwartz PJ. The congenital long QT syndromes from genotype to phenotype: clinical implications. J Intern Med 2006;259:39-47.
-
(2006)
J Intern Med
, vol.259
, pp. 39-47
-
-
Schwartz, P.J.1
-
17
-
-
33644853794
-
The Jervell and Lange-Nielsen syndrome: Natural history, molecular basis, and clinical outcome
-
Schwartz PJ, Spazzolini C, Crotti L, Bathen J, Amlie JP, Timothy K, et al. The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome. Circulation 2006;113:783-90.
-
(2006)
Circulation
, vol.113
, pp. 783-790
-
-
Schwartz, P.J.1
Spazzolini, C.2
Crotti, L.3
Bathen, J.4
Amlie, J.P.5
Timothy, K.6
-
18
-
-
0035830365
-
Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias
-
Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, et al. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation 2001;103:89-95.
-
(2001)
Circulation
, vol.103
, pp. 89-95
-
-
Schwartz, P.J.1
Priori, S.G.2
Spazzolini, C.3
Moss, A.J.4
Vincent, G.M.5
Napolitano, C.6
-
19
-
-
0038205726
-
Modulating effects of age and gender on the clinical course of long QT syndrome by genotype
-
Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, et al. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype. J Am Coll Cardiol 2003;42:103-9.
-
(2003)
J Am Coll Cardiol
, vol.42
, pp. 103-109
-
-
Zareba, W.1
Moss, A.J.2
Locati, E.H.3
Lehmann, M.H.4
Peterson, D.R.5
Hall, W.J.6
-
20
-
-
0035895322
-
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachcardia
-
Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachcardia. Circulation 2001;103:196-200.
-
(2001)
Circulation
, vol.103
, pp. 196-200
-
-
Priori, S.G.1
Napolitano, C.2
Tiso, N.3
Memmi, M.4
Vignati, G.5
Bloise, R.6
-
21
-
-
0036713510
-
Human non-synonymous SNPs: Server and survey
-
Ramensky V, Bork P, Sunayev S. Human non-synonymous SNPs: server and survey. Nucleic Acids Res 2002;30:3894-900.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunayev, S.3
-
22
-
-
29144494740
-
Genetic testing in the long QT syndrome
-
Napolitano C, Priori SG, Schwartz PJ, Bloise R, Ronchetti E, Nastoli J, et al. Genetic testing in the long QT syndrome. J Am Med Assoc 2005;294:2975-80.
-
(2005)
J Am Med Assoc
, vol.294
, pp. 2975-2980
-
-
Napolitano, C.1
Priori, S.G.2
Schwartz, P.J.3
Bloise, R.4
Ronchetti, E.5
Nastoli, J.6
-
23
-
-
0032908945
-
The inherited long-QT syndrome: From ion channel to bedside
-
Vincent GM, Timothy K, Fox J, Zhang L. The inherited long-QT syndrome: from ion channel to bedside. Cardiol Rev 1999;7:44-55.
-
(1999)
Cardiol Rev
, vol.7
, pp. 44-55
-
-
Vincent, G.M.1
Timothy, K.2
Fox, J.3
Zhang, L.4
-
24
-
-
33750348298
-
Postmortem long QT syndrome genetic testing for sudden unexplained death in the young
-
Tester DJ, Ackerman MJ. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young. J Am Coll Cardiol 2007;49:240-6.
-
(2007)
J Am Coll Cardiol
, vol.49
, pp. 240-246
-
-
Tester, D.J.1
Ackerman, M.J.2
-
25
-
-
30344476135
-
Sudden death in the young
-
Puranik R, Chow CK, Duflou JA, Kilborn MJ, McGuire MA. Sudden death in the young. Heart Rhythm 2005;2:1277-82.
-
(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
-
26
-
-
0034609531
-
Spectrum of mutations in long-QT syndrome genes
-
Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, et al. Spectrum of mutations in long-QT syndrome genes. Circulation 2000;102:1178-85.
-
(2000)
Circulation
, vol.102
, pp. 1178-1185
-
-
Splawski, I.1
Shen, J.2
Timothy, K.W.3
Lehmann, M.H.4
Priori, S.5
Robinson, J.L.6
-
27
-
-
2442657712
-
-
Fodstad H, Swan H, Laitinen P, Piippo K, Paavonen K, Viitasalo M, et al. Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland. Ann Med 2004;36Suppl 1:53-63.
-
Fodstad H, Swan H, Laitinen P, Piippo K, Paavonen K, Viitasalo M, et al. Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland. Ann Med 2004;36Suppl 1:53-63.
-
-
-
-
28
-
-
2442671474
-
-
van Langen IM, Hofman N, Tan HL, Wilde AAM. Family and population strategies for screening and counselling of inherited cardiac arrhythmias. Ann Med 2004;36Suppl 1:116-23.
-
van Langen IM, Hofman N, Tan HL, Wilde AAM. Family and population strategies for screening and counselling of inherited cardiac arrhythmias. Ann Med 2004;36Suppl 1:116-23.
-
-
-
-
29
-
-
33845905238
-
Female predominance and transmission distortion in the long-QT syndrome
-
Imboden M, Swan H, Denjoy I, Van Langen IM, Latinen-Forsblom PJ, Napolitano C, et al. Female predominance and transmission distortion in the long-QT syndrome. N Engl J Med 2006;355:2744-51.
-
(2006)
N Engl J Med
, vol.355
, pp. 2744-2751
-
-
Imboden, M.1
Swan, H.2
Denjoy, I.3
Van Langen, I.M.4
Latinen-Forsblom, P.J.5
Napolitano, C.6
-
30
-
-
26944485507
-
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing
-
Tester DJ, Kopplin LJ, Will ML, Ackerman MJ. Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing. Heart Rhythm 2005;2:1099-105.
-
(2005)
Heart Rhythm
, vol.2
, pp. 1099-1105
-
-
Tester, D.J.1
Kopplin, L.J.2
Will, M.L.3
Ackerman, M.J.4
-
31
-
-
7544230111
-
Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor 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 RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases. Mayo Clin Proc 2004;79:1380-4.
-
(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
|