-
5
-
-
1442306232
-
Drug-induced prolongation of the QT interval
-
D.M. Roden Drug-induced prolongation of the QT interval N Engl J Med 350 2004 1013-1022
-
(2004)
N Engl J Med
, vol.350
, pp. 1013-1022
-
-
Roden, D.M.1
-
6
-
-
27744471093
-
Drug-induced torsades de pointes
-
P.T. Fitzgerald M.J. Ackerman Drug-induced torsades de pointes the evolving role of pharmacogenetics Heart Rhythm 2 2005 S30-S37
-
(2005)
Heart Rhythm
, vol.2
-
-
Fitzgerald, P.T.1
Ackerman, M.J.2
-
7
-
-
0027335784
-
K1 blockade
-
K1 blockade a new antiarrhythmic mechanism? Effect of RP58866 on ventricular arrhythmias in rat, rabbit, and primate Circulation 87 1993 1979-1989
-
(1993)
Circulation
, vol.87
, pp. 1979-1989
-
-
Rees, S.A.1
Curtis, M.J.2
-
8
-
-
0028209617
-
K1 blockade is a potentially useful antiarrhythmic mechanism
-
K1 blockade is a potentially useful antiarrhythmic mechanism Cardiovasc Res 28 1994 421
-
(1994)
Cardiovasc Res
, vol.28
, pp. 421
-
-
Rees, S.A.1
Curtis, M.J.2
-
9
-
-
0028398053
-
K1 blockade is unlikely to be a useful antiarrhythmic mechanism
-
K1 blockade is unlikely to be a useful antiarrhythmic mechanism Cardiovasc Res 28 1994 420
-
(1994)
Cardiovasc Res
, vol.28
, pp. 420
-
-
Opthof, T.1
-
10
-
-
0035907032
-
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
-
N.M. Plaster R. Tawil M. Tristani-Firouzi S. Canün S. Bendahhou A. Tsunoda M.R. Donaldson S.T. Iannaccone E. Brunt R. Barohn J. Clark F. Deymeer A.L. George Jr F.A. Fish A. Hahn A. Nitu C. Ozdemir P. Serdaroglu S.H. Subramony G. Wolfe Y.H. Fu L.J. Ptácek Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome Cell 105 2001 511-519
-
(2001)
Cell
, vol.105
, pp. 511-519
-
-
Plaster, N.M.1
Tawil, R.2
Tristani-Firouzi, M.3
Canün, S.4
Bendahhou, S.5
Tsunoda, A.6
Donaldson, M.R.7
Iannaccone, S.T.8
Brunt, E.9
Barohn, R.10
Clark, J.11
Deymeer, F.12
George, A.L.13
Fish, F.A.14
Hahn, A.15
Nitu, A.16
Ozdemir, C.17
Serdaroglu, P.18
Subramony, S.H.19
Wolfe, G.20
Fu, Y.H.21
Ptácek, L.J.22
more..
-
11
-
-
0015124692
-
Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?
-
E.D. Andersen P.A. Krasilnikoff H. Overvad Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome? Acta Paediatr Scand 60 1971 559-564
-
(1971)
Acta Paediatr Scand
, vol.60
, pp. 559-564
-
-
Andersen, E.D.1
Krasilnikoff, P.A.2
Overvad, H.3
-
12
-
-
0028298042
-
Andersen's syndrome
-
R. Tawil L.J. Ptácek S.G. Pavlakis D.C. DeVivo A.S. Penn C. Ozdemir R.C. Griggs Andersen's syndrome potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features Ann Neurol 35 1994 326-330
-
(1994)
Ann Neurol
, vol.35
, pp. 326-330
-
-
Tawil, R.1
Ptácek, L.J.2
Pavlakis, S.G.3
DeVivo, D.C.4
Penn, A.S.5
Ozdemir, C.6
Griggs, R.C.7
-
13
-
-
2442682788
-
Andersen-Tawil syndrome
-
M.R. Donaldson G. Yoon Y.H. Fu L.J. Ptácek Andersen-Tawil syndrome a model of clinical variability, pleiotropy, and genetic heterogeneity Ann Med 36 suppl 1 2004 92-97
-
(2004)
Ann Med
, vol.36
, Issue.SUPPL. 1
, pp. 92-97
-
-
Donaldson, M.R.1
Yoon, G.2
Fu, Y.H.3
Ptácek, L.J.4
-
15
-
-
0036324229
-
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
-
M. Tristani-Firouzi J.L. Jensen M.R. Donaldson V. Sansone G. Meola A. Hahn S. Bendahhou H. Kwiecinski A. Fidzianska N. Plaster Y.H. Fu L.J. Ptácek R. Tawil Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) J Clin Invest 110 2002 38138-8
-
(2002)
J Clin Invest
, vol.110
-
-
Tristani-Firouzi, M.1
Jensen, J.L.2
Donaldson, M.R.3
Sansone, V.4
Meola, G.5
Hahn, A.6
Bendahhou, S.7
Kwiecinski, H.8
Fidzianska, A.9
Plaster, N.10
Fu, Y.H.11
Ptácek, L.J.12
Tawil, R.13
-
16
-
-
0037384899
-
Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome
-
Y. Hosaka H. Hanawa T. Washizuka M. Chinushi F. Yamashita T. Yoshida S. Komura H. Watanabe Y. Aizawa Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome J Mol Cell Cardiol 35 2003 409-415
-
(2003)
J Mol Cell Cardiol
, vol.35
, pp. 409-415
-
-
Hosaka, Y.1
Hanawa, H.2
Washizuka, T.3
Chinushi, M.4
Yamashita, F.5
Yoshida, T.6
Komura, S.7
Watanabe, H.8
Aizawa, Y.9
-
17
-
-
21344466555
-
In vivo and in vitro functional characterization of Andersen's syndrome mutations
-
S. Bendahhou E. Fournier D. Sternberg G. Bassez A. Furby C. Sereni M.R. Donaldson M.M. Larroque B. Fontaine J. Barhanin In vivo and in vitro functional characterization of Andersen's syndrome mutations J Physiol 565 2005 731-741
-
(2005)
J Physiol
, vol.565
, pp. 731-741
-
-
Bendahhou, S.1
Fournier, E.2
Sternberg, D.3
Bassez, G.4
Furby, A.5
Sereni, C.6
Donaldson, M.R.7
Larroque, M.M.8
Fontaine, B.9
Barhanin, J.10
-
18
-
-
0037188493
-
Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome
-
R. Preisig-Müller G. Schlichthörl T. Goerge S. Heinen A. Brüggemann S. Rajan C. Derst R.W. Veh J. Daut Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome Proc Natl Acad Sci U S A 99 2002 7774-7779
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 7774-7779
-
-
Preisig-Müller, R.1
Schlichthörl, G.2
Goerge, T.3
Heinen, S.4
Brüggemann, A.5
Rajan, S.6
Derst, C.7
Veh, R.W.8
Daut, J.9
-
19
-
-
0037975497
-
Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression
-
J. Miake E. Marbán H.B. Nuss Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression J Clin Invest 111 2003 1529-1536
-
(2003)
J Clin Invest
, vol.111
, pp. 1529-1536
-
-
Miake, J.1
Marbán, E.2
Nuss, H.B.3
-
20
-
-
0042859880
-
Short QT Syndrome
-
F. Gaita C. Giustetto F. Bianchi C. Wolpert R. Schimpf R. Riccardi S. Grossi E. Richiardi M. Borggrefe Short QT Syndrome a familial cause of sudden death Circulation 108 2003 965-970
-
(2003)
Circulation
, vol.108
, pp. 965-970
-
-
Gaita, F.1
Giustetto, C.2
Bianchi, F.3
Wolpert, C.4
Schimpf, R.5
Riccardi, R.6
Grossi, S.7
Richiardi, E.8
Borggrefe, M.9
-
22
-
-
20244364402
-
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene
-
S.G. Priori S.V. Pandit I. Rivolta O. Berenfeld E. Ronchetti A. Dhamoon C. Napolitano J. Anumonwo M.R. di Barletta S. Gudapakkam G. Bosi M. Stramba-Badiale J. Jalife A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene Circ Res 96 2005 800-707
-
(2005)
Circ Res
, vol.96
-
-
Priori, S.G.1
Pandit, S.V.2
Rivolta, I.3
Berenfeld, O.4
Ronchetti, E.5
Dhamoon, A.6
Napolitano, C.7
Anumonwo, J.8
di Barletta, M.R.9
Gudapakkam, S.10
Bosi, G.11
Stramba-Badiale, M.12
Jalife, J.13
-
24
-
-
17644399838
-
Short QT syndrome or Andersen syndrome
-
E. Schulze-Bahr Short QT syndrome or Andersen syndrome yin and yang of Kir2.1 channel dysfunction Circ Res 96 2005 703-704
-
(2005)
Circ Res
, vol.96
, pp. 703-704
-
-
Schulze-Bahr, E.1
-
25
-
-
20344388309
-
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations
-
L. Zhang D.W. Benson M. Tristani-Firouzi L.J. Ptácek R. Tawil P.J. Schwartz A.L. George M. Horie G. Andelfinger G.L. Snow Y.H. Fu M.J. Ackerman G.M. Vincent Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations characteristic T-U-wave patterns predict the KCNJ2 genotype Circulation 111 2005 2720-2726
-
(2005)
Circulation
, vol.111
, pp. 2720-2726
-
-
Zhang, L.1
Benson, D.W.2
Tristani-Firouzi, M.3
Ptácek, L.J.4
Tawil, R.5
Schwartz, P.J.6
George, A.L.7
Horie, M.8
Andelfinger, G.9
Snow, G.L.10
Fu, Y.H.11
Ackerman, M.J.12
Vincent, G.M.13
-
26
-
-
0037777713
-
2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
-
2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome Neurology 60 2003 1811-1816
-
(2003)
Neurology
, vol.60
, pp. 1811-1816
-
-
Donaldson, M.R.1
Jensen, J.L.2
Tristani-Firouzi, M.3
Tawil, R.4
Bendahhou, S.5
Suarez, W.A.6
Cobo, A.M.7
Poza, J.J.8
Behr, E.9
Wagstaff, J.10
Szepetowski, P.11
Pereira, S.12
Mozaffar, T.13
Escolar, D.M.14
Fu, Y.H.15
Ptácek, L.J.16
-
27
-
-
26444448949
-
Andersen-Tawil syndrome
-
N.P. Davies P. Imbrici D. Fialho C. Herd L.G. Bilsland A. Weber R. Mueller D. Hilton-Jones J. Ealing B.R. Boothman P. Giunti L.M. Parsons M. Thomas A.Y. Manzur K. Jurkat-Rott F. Lehmann-Horn P.F. Chinnery M. Rose D.M. Kullmann M.G. Hanna Andersen-Tawil syndrome new potassium channel mutations and possible phenotypic variation Neurology 65 2005 1083-1089
-
(2005)
Neurology
, vol.65
, pp. 1083-1089
-
-
Davies, N.P.1
Imbrici, P.2
Fialho, D.3
Herd, C.4
Bilsland, L.G.5
Weber, A.6
Mueller, R.7
Hilton-Jones, D.8
Ealing, J.9
Boothman, B.R.10
Giunti, P.11
Parsons, L.M.12
Thomas, M.13
Manzur, A.Y.14
Jurkat-Rott, K.15
Lehmann-Horn, F.16
Chinnery, P.F.17
Rose, M.18
Kullmann, D.M.19
Hanna, M.G.20
more..
-
29
-
-
33144477356
-
Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7)
-
M. Tsuboi C. Antzelevitch Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7) Heart Rhythm 3 2006 328-335
-
(2006)
Heart Rhythm
, vol.3
, pp. 328-335
-
-
Tsuboi, M.1
Antzelevitch, C.2
-
31
-
-
0027460628
-
Ionic bases for electrophysiological distinctions among epicardial, midmyocardial, and endocardial myocytes from the free wall of the canine left ventricle
-
D.W. Liu G.A. Gintant C. Antzelevitch Ionic bases for electrophysiological distinctions among epicardial, midmyocardial, and endocardial myocytes from the free wall of the canine left ventricle Circ Res 72 1993 671-687
-
(1993)
Circ Res
, vol.72
, pp. 671-687
-
-
Liu, D.W.1
Gintant, G.A.2
Antzelevitch, C.3
-
32
-
-
20444372298
-
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation
-
M. Xia Q. Jin S. Bendahhou Y. He M.M. Larroque Y. Chen Q. Zhou Y. Yang Y. Liu B. Liu Q. Zhu Y. Zhou J. Lin B. Liang L. Li X. Dong Z. Pan R. Wang H. Wan W. Qiu W. Xu P. Eurlings J. Barhanin Y. Chen A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation Biochem Biophys Res Commun 332 2005 1012-1019
-
(2005)
Biochem Biophys Res Commun
, vol.332
, pp. 1012-1019
-
-
Xia, M.1
Jin, Q.2
Bendahhou, S.3
He, Y.4
Larroque, M.M.5
Chen, Y.6
Zhou, Q.7
Yang, Y.8
Liu, Y.9
Liu, B.10
Zhu, Q.11
Zhou, Y.12
Lin, J.13
Liang, B.14
Li, L.15
Dong, X.16
Pan, Z.17
Wang, R.18
Wan, H.19
Qiu, W.20
Xu, W.21
Eurlings, P.22
Barhanin, J.23
Chen, Y.24
more..
|