-
1
-
-
79959924214
-
Sudden cardiac arrest without overt heart disease
-
Modi S, Krahn AD. Sudden cardiac arrest without overt heart disease. Circulation. 2011;123(25):2994-3008.
-
(2011)
Circulation.
, vol.123
, Issue.25
, pp. 2994-3008
-
-
Modi, S.1
Krahn, A.D.2
-
2
-
-
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(3):250-269.
-
(1998)
Mayo Clin Proc.
, vol.73
, Issue.3
, pp. 250-269
-
-
Ackerman, M.J.1
-
3
-
-
59649127401
-
Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy
-
Johnson JN, Hofman N, Haglund CM, Cascino GD, Wilde AA, Ackerman MJ. Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy. Neurology. 2009;72(3):224-231.
-
(2009)
Neurology.
, vol.72
, Issue.3
, pp. 224-231
-
-
Johnson, J.N.1
Hofman, N.2
Haglund, C.M.3
Cascino, G.D.4
Wilde, A.A.5
Ackerman, M.J.6
-
4
-
-
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(1):44-55.
-
(1999)
Cardiol Rev
, vol.7
, Issue.1
, pp. 44-55
-
-
Vincent, G.M.1
Timothy, K.2
Fox, J.3
Zhang, L.4
-
5
-
-
68949209933
-
Spectrum and prevalence of mutations from the first 2,500 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 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm. 2009;6(9):1297-1303.
-
(2009)
Heart Rhythm.
, vol.6
, Issue.9
, pp. 1297-1303
-
-
Kapplinger, J.D.1
Tester, D.J.2
Salisbury, B.A.3
-
6
-
-
49749174698
-
Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death
-
Jervell A, Lange-Nielsen F. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death. Am Heart J. 1957;54(1):59-68.
-
(1957)
Am Heart J.
, vol.54
, Issue.1
, pp. 59-68
-
-
Jervell, A.1
Lange-Nielsen, F.2
-
7
-
-
0031054075
-
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange- Nielsen cardioauditory syndrome
-
Neyroud N, Tesson F, Denjoy I, et al. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange- Nielsen cardioauditory syndrome. Nat Genet. 1997;15(2):186-189.
-
(1997)
Nat Genet.
, vol.15
, Issue.2
, pp. 186-189
-
-
Neyroud, N.1
Tesson, F.2
Denjoy, I.3
-
8
-
-
70449359365
-
Genetic testing for long-QT syndrome: Distinguishing pathogenic mutations from benign variants
-
Kapa S, Tester DJ, Salisbury BA, et al. Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants. Circulation. 2009;120(18):1752-1760.
-
(2009)
Circulation.
, vol.120
, Issue.18
, pp. 1752-1760
-
-
Kapa, S.1
Tester, D.J.2
Salisbury, B.A.3
-
9
-
-
0037623309
-
Implantable cardioverter defibrillator in high-risk long QT syndrome patients
-
Zareba W, Moss AJ, Daubert JP, Hall WJ, Robinson JL, Andrews M. Implantable cardioverter defibrillator in high-risk long QT syndrome patients. J Cardiovasc Electrophysiol. 2003; 14(4):337-341.
-
(2003)
J Cardiovasc Electrophysiol.
, vol.14
, Issue.4
, pp. 337-341
-
-
Zareba, W.1
Moss, A.J.2
Daubert, J.P.3
Hall, W.J.4
Robinson, J.L.5
Andrews, M.6
-
10
-
-
46349104535
-
ACC/AHA/HRS 2008 guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: Executive summary
-
Epstein AE, Dimarco JP, Ellenbogen KA, et al. ACC/AHA/HRS 2008 guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: executive summary. Heart Rhythm. 2008;5(6):934-955.
-
(2008)
Heart Rhythm
, vol.5
, Issue.6
, pp. 934-955
-
-
Epstein, A.E.1
Dimarco, J.P.2
Ellenbogen, K.A.3
-
11
-
-
0026874017
-
Syncope: Brain or heart? a case report
-
Nilsson H, Freitag M, Hindfelt B, Johansson BW, Rosen I. Syncope: brain or heart? a case report. Pacing Clin Electrophysiol. 1992;15(6):957-960.
-
(1992)
Pacing Clin Electrophysiol.
, vol.15
, Issue.6
, pp. 957-960
-
-
Nilsson, H.1
Freitag, M.2
Hindfelt, B.3
Johansson, B.W.4
Rosen, I.5
-
12
-
-
0028292927
-
A family of potassium channel genes related to eag in Drosophila and mammals
-
Warmke JW, Ganetzky B. A family of potassium channel genes related to eag in Drosophila and mammals. Proc Natl Acad Sci U S A. 1994;91(8):3438-3442.
-
(1994)
Proc Natl Acad Sci U S A.
, vol.91
, Issue.8
, pp. 3438-3442
-
-
Warmke, J.W.1
Ganetzky, B.2
-
13
-
-
0033568854
-
Impaired K(-) homeostasis and altered electrophysiological properties of post-traumatic hippocampal glia
-
D'Ambrosio R, Maris DO, Grady MS, Winn HR, Janigro D. Impaired K(-) homeostasis and altered electrophysiological properties of post-traumatic hippocampal glia. J Neurosci. 1999;19(18):8152-8162.
-
(1999)
J Neurosci.
, vol.19
, Issue.18
, pp. 8152-8162
-
-
D'Ambrosio, R.1
Maris, D.O.2
Grady, M.S.3
Winn, H.R.4
Janigro, D.5
-
14
-
-
0030946545
-
Reduction of K- uptake in glia prevents long-term depression maintenance and causes epileptiform activity
-
Janigro D, Gasparini S, D'Ambrosio R, McKhann G II, DiFrancesco D. Reduction of K- uptake in glia prevents long-term depression maintenance and causes epileptiform activity. J Neurosci. 1997;17(8):2813-2824.
-
(1997)
J Neurosci.
, vol.17
, Issue.8
, pp. 2813-2824
-
-
Janigro, D.1
Gasparini, S.2
D'Ambrosio, R.3
McKhann, I.I.G.4
Difrancesco, D.5
-
15
-
-
0025730269
-
Magnetic resonance imaging-based volume studies in temporal lobe epilepsy: Pathological correlations
-
Cascino GD, Jack CR Jr, Parisi JE, et al. Magnetic resonance imaging-based volume studies in temporal lobe epilepsy: pathological correlations. Ann Neurol. 1991;30(1):31-36.
-
(1991)
Ann Neurol.
, vol.30
, Issue.1
, pp. 31-36
-
-
Cascino, G.D.1
Jack Jr., C.R.2
Parisi, J.E.3
-
16
-
-
59649084698
-
Seizures and arrhythmias: Differing phenotypes of a common channelopathy?
-
Hunter JV, Moss AJ. Seizures and arrhythmias: differing phenotypes of a common channelopathy? Neurology. 2009; 72(3):208-209.
-
(2009)
Neurology
, vol.72
, Issue.3
, pp. 208-209
-
-
Hunter, J.V.1
Moss, A.J.2
|