-
1
-
-
70449367296
-
Prevalence of the congenital long-QT syndrome
-
2-s2.0-70449367296 10.1161/CIRCULATIONAHA.109.863209
-
Schwartz P. J., Stramba-Badiale M., Crotti L., Pedrazzini M., Besana A., Bosi G., Gabbarini F., Goulene K., Insolia R., Mannarino S., Mosca F., Nespoli L., Rimini A., Rosati E., Salice P., Spazzolini C., Prevalence of the congenital long-QT syndrome. Circulation 2009 120 18 1761 1767 2-s2.0-70449367296 10.1161/CIRCULATIONAHA.109.863209
-
(2009)
Circulation
, vol.120
, Issue.18
, pp. 1761-1767
-
-
Schwartz, P.J.1
Stramba-Badiale, M.2
Crotti, L.3
Pedrazzini, M.4
Besana, A.5
Bosi, G.6
Gabbarini, F.7
Goulene, K.8
Insolia, R.9
Mannarino, S.10
Mosca, F.11
Nespoli, L.12
Rimini, A.13
Rosati, E.14
Salice, P.15
Spazzolini, C.16
-
2
-
-
84863349113
-
Sudden cardiac death and inherited channelopathy: The basic electrophysiology of the myocyte and myocardium in ion channel disease
-
Martin C. A., Matthews G. D., Huang C. L., Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease. Heart 2012 98 7 536 543
-
(2012)
Heart
, vol.98
, Issue.7
, pp. 536-543
-
-
Martin, C.A.1
Matthews, G.D.2
Huang, C.L.3
-
3
-
-
70349452265
-
Cardiac ion channels
-
Grant A. O., Cardiac ion channels. Circulation 2009 2 2 185 194
-
(2009)
Circulation
, vol.2
, Issue.2
, pp. 185-194
-
-
Grant, A.O.1
-
4
-
-
50149112857
-
The QT syndromes: Long and short
-
2-s2.0-50149112857 10.1016/S0140-6736(08)61307-0
-
Morita H., Wu J., Zipes D. P., The QT syndromes: long and short. The Lancet 2008 372 9640 750 763 2-s2.0-50149112857 10.1016/S0140-6736(08)61307-0
-
(2008)
The Lancet
, vol.372
, Issue.9640
, pp. 750-763
-
-
Morita, H.1
Wu, J.2
Zipes, D.P.3
-
5
-
-
36248966518
-
Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors
-
DOI 10.1016/j.cell.2007.11.019, PII S0092867407014717
-
Takahashi K., Tanabe K., Ohnuki M., Narita M., Ichisaka T., Tomoda K., Yamanaka S., Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 2007 131 5 861 872 2-s2.0-36248966518 10.1016/j.cell.2007.11.019 (Pubitemid 350138099)
-
(2007)
Cell
, vol.131
, Issue.5
, pp. 861-872
-
-
Takahashi, K.1
Tanabe, K.2
Ohnuki, M.3
Narita, M.4
Ichisaka, T.5
Tomoda, K.6
Yamanaka, S.7
-
6
-
-
36749043230
-
Induced pluripotent stem cell lines derived from human somatic cells
-
2-s2.0-36749043230 10.1126/science.1151526
-
Yu J., Vodyanik M. A., Smuga-Otto K., Antosiewicz-Bourget J., Frane J. L., Tian S., Nie J., Jonsdottir G. A., Ruotti V., Stewart R., Slukvin I. I., Thomson J. A., Induced pluripotent stem cell lines derived from human somatic cells. Science 2007 318 5858 1917 1920 2-s2.0-36749043230 10.1126/science. 1151526
-
(2007)
Science
, vol.318
, Issue.5858
, pp. 1917-1920
-
-
Yu, J.1
Vodyanik, M.A.2
Smuga-Otto, K.3
Antosiewicz-Bourget, J.4
Frane, J.L.5
Tian, S.6
Nie, J.7
Jonsdottir, G.A.8
Ruotti, V.9
Stewart, R.10
Slukvin, I.I.11
Thomson, J.A.12
-
7
-
-
84874063703
-
A hierarchy in reprogramming capacity in different tissue microenvironments: What we know and what we need to know
-
10.1089/scd. 2012.0461
-
Liebau S., Mahaddalkar P. U., Kestler H. A., Illing A., Seufferlein T., Kleger A., A hierarchy in reprogramming capacity in different tissue microenvironments: what we know and what we need to know. Stem Cells and Development 2013 22 5 695 706 10.1089/scd. 2012.0461
-
(2013)
Stem Cells and Development
, vol.22
, Issue.5
, pp. 695-706
-
-
Liebau, S.1
Mahaddalkar, P.U.2
Kestler, H.A.3
Illing, A.4
Seufferlein, T.5
Kleger, A.6
-
8
-
-
84859742731
-
The potential of iPS cells in synucleinopathy research
-
629230
-
Linta L., Stockmann M., Boeckers T. M., Kleger A., Liebau S., The potential of iPS cells in synucleinopathy research. Stem Cells and Development 2012 2012 6 629230
-
(2012)
Stem Cells and Development
, vol.2012
, pp. 6
-
-
Linta, L.1
Stockmann, M.2
Boeckers, T.M.3
Kleger, A.4
Liebau, S.5
-
9
-
-
84859439101
-
Increased reprogramming capacity of mouse liver progenitor cells, compared with differentiated liver cells, requires the BAF complex
-
Kleger A., Mahaddalkar P. U., Katz S. F., Lechel A., Joo J. Y., Loya K., Increased reprogramming capacity of mouse liver progenitor cells, compared with differentiated liver cells, requires the BAF complex. Gastroenterology 2012 142 4 907 917
-
(2012)
Gastroenterology
, vol.142
, Issue.4
, pp. 907-917
-
-
Kleger, A.1
Mahaddalkar, P.U.2
Katz, S.F.3
Lechel, A.4
Joo, J.Y.5
Loya, K.6
-
10
-
-
70349437501
-
Generation of pluripotent stem cells from patients with type 1 diabetes
-
2-s2.0-70349437501 10.1073/pnas.0906894106
-
Maehr R., Chen S., Snitow M., Ludwig T., Yagasaki L., Goland R., Leibel R. L., Melton D. A., Generation of pluripotent stem cells from patients with type 1 diabetes. Proceedings of the National Academy of Sciences of the United States of America 2009 106 37 15768 15773 2-s2.0-70349437501 10.1073/pnas.0906894106
-
(2009)
Proceedings of the National Academy of Sciences of the United States of America
, vol.106
, Issue.37
, pp. 15768-15773
-
-
Maehr, R.1
Chen, S.2
Snitow, M.3
Ludwig, T.4
Yagasaki, L.5
Goland, R.6
Leibel, R.L.7
Melton, D.A.8
-
11
-
-
67650095306
-
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells
-
2-s2.0-67650095306 10.1038/nature08129
-
Raya A., Rodríguez-Piz I., Guenechea G., Vassena R., Navarro S., Barrero M. J., Consiglio A., Castell M., Río P., Sleep E., González F., Tiscornia G., Garreta E., Aasen T., Veiga A., Verma I. M., Surrallés J., Bueren J., Belmonte J. C. I., Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells. Nature 2009 460 7251 53 59 2-s2.0-67650095306 10.1038/nature08129
-
(2009)
Nature
, vol.460
, Issue.7251
, pp. 53-59
-
-
Raya, A.1
Rodríguez-Piz, I.2
Guenechea, G.3
Vassena, R.4
Navarro, S.5
Barrero, M.J.6
Consiglio, A.7
Castell, M.8
Río, P.9
Sleep, E.10
González, F.11
Tiscornia, G.12
Garreta, E.13
Aasen, T.14
Veiga, A.15
Verma, I.M.16
Surrallés, J.17
Bueren, J.18
Belmonte, J.C.I.19
-
12
-
-
77956354416
-
Modeling inherited metabolic disorders of the liver using human induced pluripotent stem cells
-
2-s2.0-77956354416 10.1172/JCI43122
-
Rashid S. T., Corbineau S., Hannan N., Marciniak S. J., Miranda E., Alexander G., Huang-Doran I., Griffin J., Ahrlund-Richter L., Skepper J., Semple R., Weber A., Lomas D. A., Vallier L., Modeling inherited metabolic disorders of the liver using human induced pluripotent stem cells. Journal of Clinical Investigation 2010 120 9 3127 3136 2-s2.0-77956354416 10.1172/JCI43122
-
(2010)
Journal of Clinical Investigation
, vol.120
, Issue.9
, pp. 3127-3136
-
-
Rashid, S.T.1
Corbineau, S.2
Hannan, N.3
Marciniak, S.J.4
Miranda, E.5
Alexander, G.6
Huang-Doran, I.7
Griffin, J.8
Ahrlund-Richter, L.9
Skepper, J.10
Semple, R.11
Weber, A.12
Lomas, D.A.13
Vallier, L.14
-
13
-
-
79954626173
-
Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome
-
2-s2.0-79954626173 10.1038/nature09879
-
Liu G. H., Barkho B. Z., Ruiz S., Diep D., Qu J., Yang S. L., Panopoulos A. D., Suzuki K., Kurian L., Walsh C., Thompson J., Boue S., Fung H. L., Sancho-Martinez I., Zhang K., Iii J. Y., Belmonte J. C. I., Recapitulation of premature ageing with iPSCs from Hutchinson-Gilford progeria syndrome. Nature 2011 472 7342 221 227 2-s2.0-79954626173 10.1038/nature09879
-
(2011)
Nature
, vol.472
, Issue.7342
, pp. 221-227
-
-
Liu, G.H.1
Barkho, B.Z.2
Ruiz, S.3
Diep, D.4
Qu, J.5
Yang, S.L.6
Panopoulos, A.D.7
Suzuki, K.8
Kurian, L.9
Walsh, C.10
Thompson, J.11
Boue, S.12
Fung, H.L.13
Sancho-Martinez, I.14
Zhang, K.15
Iii, J.Y.16
Belmonte, J.C.I.17
-
14
-
-
79955884485
-
Modelling schizophrenia using human induced pluripotent stem cells
-
Brennand K. J., Simone A., Jou J., Gelboin-Burkhart C., Tran N., Sangar S., Modelling schizophrenia using human induced pluripotent stem cells. Nature 2011 473 221 225
-
(2011)
Nature
, vol.473
, pp. 221-225
-
-
Brennand, K.J.1
Simone, A.2
Jou, J.3
Gelboin-Burkhart, C.4
Tran, N.5
Sangar, S.6
-
15
-
-
79952446402
-
Modelling the long QT syndrome with induced pluripotent stem cells
-
Itzhaki I., Maizels L., Huber I., Zwi-Dantsis L., Caspi O., Winterstern A., Modelling the long QT syndrome with induced pluripotent stem cells. Nature 2011 471 7337 225 229
-
(2011)
Nature
, vol.471
, Issue.7337
, pp. 225-229
-
-
Itzhaki, I.1
Maizels, L.2
Huber, I.3
Zwi-Dantsis, L.4
Caspi, O.5
Winterstern, A.6
-
16
-
-
84867007532
-
Modeling supravalvular aortic stenosis syndrome with human induced pluripotent stem cells
-
Ge X., Ren Y., Bartulos O., Lee M. Y., Yue Z., Kim K. Y., Modeling supravalvular aortic stenosis syndrome with human induced pluripotent stem cells. Circulation 2012 126 14 1695 1704
-
(2012)
Circulation
, vol.126
, Issue.14
, pp. 1695-1704
-
-
Ge, X.1
Ren, Y.2
Bartulos, O.3
Lee, M.Y.4
Yue, Z.5
Kim, K.Y.6
-
17
-
-
84863213874
-
Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease
-
Davis R. P., Casini S., van den Berg C. W., Hoekstra M., Remme C. A., Dambrot C., Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease. Circulation 2012 125 25 3079 3091
-
(2012)
Circulation
, vol.125
, Issue.25
, pp. 3079-3091
-
-
Davis, R.P.1
Casini, S.2
Van Den Berg, C.W.3
Hoekstra, M.4
Remme, C.A.5
Dambrot, C.6
-
18
-
-
84860156650
-
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy
-
130ra47
-
Sun N., Yazawa M., Liu J., Han L., Sanchez-Freire V., Abilez O. J., Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy. Science Translational Medicine 2012 4 130 130ra47
-
(2012)
Science Translational Medicine
, vol.4
, Issue.130
-
-
Sun, N.1
Yazawa, M.2
Liu, J.3
Han, L.4
Sanchez-Freire, V.5
Abilez, O.J.6
-
19
-
-
84858129398
-
Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia
-
Jung C. B., Moretti A., Mederos y Schnitzler M., Iop L., Storch U., Bellin M., Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia. EMBO Molecular Medicine 2012 4 3 180 191
-
(2012)
EMBO Molecular Medicine
, vol.4
, Issue.3
, pp. 180-191
-
-
Jung, C.B.1
Moretti, A.2
Mederos, Y.3
Schnitzler, M.4
Iop, L.5
Storch, U.6
Bellin, M.7
-
20
-
-
79952438377
-
Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome
-
2-s2.0-79952438377 10.1038/nature09855
-
Yazawa M., Hsueh B., Jia X., Pasca A. M., Bernstein J. A., Hallmayer J., Dolmetsch R. E., Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome. Nature 2011 471 7337 230 236 2-s2.0-79952438377 10.1038/nature09855
-
(2011)
Nature
, vol.471
, Issue.7337
, pp. 230-236
-
-
Yazawa, M.1
Hsueh, B.2
Jia, X.3
Pasca, A.M.4
Bernstein, J.A.5
Hallmayer, J.6
Dolmetsch, R.E.7
-
21
-
-
49649096192
-
Generation of functional murine cardiac myocytes from induced pluripotent stem cells
-
2-s2.0-49649096192 10.1161/CIRCULATIONAHA.108.778795
-
Mauritz C., Schwanke K., Reppel M., Neef S., Katsirntaki K., Maier L. S., Nguemo F., Menke S., Haustein M., Hescheler J., Hasenfuss G., Martin U., Generation of functional murine cardiac myocytes from induced pluripotent stem cells. Circulation 2008 118 5 507 517 2-s2.0-49649096192 10.1161/CIRCULATIONAHA. 108.778795
-
(2008)
Circulation
, vol.118
, Issue.5
, pp. 507-517
-
-
Mauritz, C.1
Schwanke, K.2
Reppel, M.3
Neef, S.4
Katsirntaki, K.5
Maier, L.S.6
Nguemo, F.7
Menke, S.8
Haustein, M.9
Hescheler, J.10
Hasenfuss, G.11
Martin, U.12
-
22
-
-
77953443251
-
Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome
-
2-s2.0-77953443251 10.1038/nature09005
-
Carvajal-Vergara X., Sevilla A., Dsouza S. L., Ang Y. S., Schaniel C., Lee D. F., Yang L., Kaplan A. D., Adler E. D., Rozov R., Ge Y., Cohen N., Edelmann L. J., Chang B., Waghray A., Su J., Pardo S., Lichtenbelt K. D., Tartaglia M., Gelb B. D., Lemischka I. R., Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome. Nature 2010 465 7299 808 812 2-s2.0-77953443251 10.1038/nature09005
-
(2010)
Nature
, vol.465
, Issue.7299
, pp. 808-812
-
-
Carvajal-Vergara, X.1
Sevilla, A.2
Dsouza, S.L.3
Ang, Y.S.4
Schaniel, C.5
Lee, D.F.6
Yang, L.7
Kaplan, A.D.8
Adler, E.D.9
Rozov, R.10
Ge, Y.11
Cohen, N.12
Edelmann, L.J.13
Chang, B.14
Waghray, A.15
Su, J.16
Pardo, S.17
Lichtenbelt, K.D.18
Tartaglia, M.19
Gelb, B.D.20
Lemischka, I.R.21
more..
-
23
-
-
19244371485
-
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome
-
Donger C., Denjoy I., Berthet M., Neyroud N., Cruaud C., Bennaceur M., Chivoret G., Schwartz K., Coumel P., Guicheney P., KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome. Circulation 1997 96 9 2778 2781 2-s2.0-19244371485 (Pubitemid 27500069)
-
(1997)
Circulation
, vol.96
, Issue.9
, pp. 2778-2781
-
-
Donger, C.1
Denjoy, I.2
Berthet, M.3
Neyroud, N.4
Cruaud, C.5
Bennaceur, M.6
Chivoret, G.7
Schwartz, K.8
Coumel, P.9
Guicheney, P.10
-
24
-
-
0034163543
-
Differential effects of beta-adrenergic agonists and antagonist in LQT1, LQT2 and LQT3 models of the long QT syndrome
-
DOI 10.1016/S0735-1097(99)00582-3, PII S0735109799005823
-
Shimizu W., Antzelevitch C., Differential effects of beta-adrenergic agonists and antagonist in LQT1, LQT2 and LQT3 models of the long QT syndrome. Journal of the American College of Cardiology 2000 35 3 778 786 2-s2.0-0034163543 10.1016/S0735-1097(99)00582-3 (Pubitemid 30167037)
-
(2000)
Journal of the American College of Cardiology
, vol.35
, Issue.3
, pp. 778-786
-
-
Shimizu, W.1
Antzelevitch, C.2
-
25
-
-
77957729169
-
Patient-specific induced pluripotent stem-cell models for long-QT syndrome
-
Moretti A., Bellin M., Welling A., Jung C. B., Lam J. T., Bott-Flugel L., Patient-specific induced pluripotent stem-cell models for long-QT syndrome. The New England Journal of Medicine 2010 363 15 1397 1409
-
(2010)
The New England Journal of Medicine
, vol.363
, Issue.15
, pp. 1397-1409
-
-
Moretti, A.1
Bellin, M.2
Welling, A.3
Jung, C.B.4
Lam, J.T.5
Bott-Flugel, L.6
-
26
-
-
79954523845
-
Drug evaluation in cardiomyocytes derived from human induced pluripotent stem cells carrying a long QT syndrome type 2 mutation
-
2-s2.0-79954523845 10.1093/eurheartj/ehr073
-
Matsa E., Rajamohan D., Dick E., Young L., Mellor I., Staniforth A., Denning C., Drug evaluation in cardiomyocytes derived from human induced pluripotent stem cells carrying a long QT syndrome type 2 mutation. European Heart Journal 2011 32 8 952 962 2-s2.0-79954523845 10.1093/eurheartj/ehr073
-
(2011)
European Heart Journal
, vol.32
, Issue.8
, pp. 952-962
-
-
Matsa, E.1
Rajamohan, D.2
Dick, E.3
Young, L.4
Mellor, I.5
Staniforth, A.6
Denning, C.7
-
27
-
-
84858040591
-
Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture
-
Lahti A. L., Kujala V. J., Chapman H., Koivisto A. P., Pekkanen-Mattila M., Kerkela E., Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture. Disease Models and Mechanisms 2012 5 2 220 230
-
(2012)
Disease Models and Mechanisms
, vol.5
, Issue.2
, pp. 220-230
-
-
Lahti, A.L.1
Kujala, V.J.2
Chapman, H.3
Koivisto, A.P.4
Pekkanen-Mattila, M.5
Kerkela, E.6
-
28
-
-
80053574096
-
Cardiomyocytes obtained from induced pluripotent stem cells with long-QT syndrome 3 recapitulate typical disease-specific features in vitro
-
Malan D., Friedrichs S., Fleischmann B. K., Sasse P., Cardiomyocytes obtained from induced pluripotent stem cells with long-QT syndrome 3 recapitulate typical disease-specific features in vitro. Circulation Research 2011 109 8 841 847
-
(2011)
Circulation Research
, vol.109
, Issue.8
, pp. 841-847
-
-
Malan, D.1
Friedrichs, S.2
Fleischmann, B.K.3
Sasse, P.4
-
29
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
2-s2.0-0028914969 10.1016/0092-8674(95)90358-5
-
Curran M. E., Splawski I., Timothy K. W., Vincent G. M., Green E. D., Keating M. T., A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 1995 80 5 795 803 2-s2.0-0028914969 10.1016/0092-8674(95) 90358-5
-
(1995)
Cell
, vol.80
, Issue.5
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
Vincent, G.M.4
Green, E.D.5
Keating, M.T.6
-
30
-
-
4544387969
-
Association of long QT syndrome loci and cardiac events among patients treated with β-blockers
-
DOI 10.1001/jama.292.11.1341
-
Priori S. G., Napolitano C., Schwartz P. J., Grillo M., Bloise R., Ronchetti E., Moncalvo C., Tulipani C., Veia A., Bottelli G., Nastoli J., Association of long QT syndrome loci and cardiac events among patients treated with β -blockers. Journal of the American Medical Association 2004 292 11 1341 1344 2-s2.0-4544387969 10.1001/jama.292.11.1341 (Pubitemid 39223225)
-
(2004)
Journal of the American Medical Association
, vol.292
, Issue.11
, pp. 1341-1344
-
-
Priori, S.G.1
Napolitano, C.2
Schwartz, P.J.3
Grillo, M.4
Bloise, R.5
Ronchetti, E.6
Moncalvo, C.7
Tulipani, C.8
Veia, A.9
Bottelli, G.10
Nastoli, J.11
-
31
-
-
0035830365
-
Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias
-
Schwartz P. J., Priori S. G., Spazzolini C., Moss A. J., Michael Vincent G., Napolitano C., Denjoy I., Guicheney P., Breithardt G., Keating M. T., Towbin J. A., Beggs A. H., Brink P., Wilde A. A. M., Toivonen L., Zareba W., Robinson J. L., Timothy K. W., Corfield V., Wattanasirichaigoon D., Corbett C., Haverkamp W., Schulze-Bahr E., Lehmann M. H., Schwartz K., Coumel P., Bloise R., Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation 2001 103 1 89 95 2-s2.0-0035830365 (Pubitemid 32050441)
-
(2001)
Circulation
, vol.103
, Issue.1
, pp. 89-95
-
-
Schwartz, P.J.1
Priori, S.G.2
Spazzolini, C.3
Moss, A.J.4
Michael Vincent, G.5
Napolitano, C.6
Denjoy, I.7
Guicheney, P.8
Breithardt, G.9
Keating, M.T.10
Towbin, J.A.11
Beggs, A.H.12
Brink, P.13
Wilde, A.A.M.14
Toivonen, L.15
Zareba, W.16
Robinson, J.L.17
Timothy, K.W.18
Corfield, V.19
Wattanasirichaigoon, D.20
Corbett, C.21
Haverkamp, W.22
Schulze-Bahr, E.23
Lehmann, M.H.24
Schwartz, K.25
Coumel, P.26
Bloise, R.27
more..
-
32
-
-
9644264340
-
Classification and mechanism of Torsade de Pointes initiation in patients with congenital long QT syndrome
-
DOI 10.1016/j.ehj.2004.08.020, PII S0195668X04006104
-
Noda T., Shimizu W., Satomi K., Suyama K., Kurita T., Aihara N., Kamakura S., Classification and mechanism of Torsade de Pointes initiation in patients with congenital long QT syndrome. European Heart Journal 2004 25 23 2149 2154 2-s2.0-9644264340 10.1016/j.ehj.2004.08.020 (Pubitemid 39572248)
-
(2004)
European Heart Journal
, vol.25
, Issue.23
, pp. 2149-2154
-
-
Noda, T.1
Shimizu, W.2
Satomi, K.3
Suyama, K.4
Kurita, T.5
Aihara, N.6
Kamakura, S.7
-
33
-
-
0036623671
-
Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome
-
DOI 10.1053/euhj.2001.3079
-
Noda T., Takaki H., Kurita T., Suyama K., Nagaya N., Taguchi A., Aihara N., Kamakura S., Sunagawa K., Nakamura K., Ohe T., Horie M., Napolitano C., Towbin J. A., Priori S. G., Shimizu W., Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome. European Heart Journal 2002 23 12 975 983 2-s2.0-0036623671 10.1053/euhj.2001.3079 (Pubitemid 35203877)
-
(2002)
European Heart Journal
, vol.23
, Issue.12
, pp. 975-983
-
-
Noda, T.1
Takaki, H.2
Kurita, T.3
Suyama, K.4
Nagaya, N.5
Taguchi, A.6
Aihara, N.7
Kamakura, S.8
Sunagawa, K.9
Nakamura, K.10
Ohe, T.11
Horie, M.12
Napolitano, C.13
Towbin, J.A.14
Priori, S.G.15
Shimizu, W.16
-
34
-
-
42649145054
-
Prevalence of early-onset atrial fibrillation in congenital long QT syndrome
-
2-s2.0-42649145054 10.1016/j.hrthm.2008.02.007
-
Johnson J. N., Tester D. J., Perry J., Salisbury B. A., Reed C. R., Ackerman M. J., Prevalence of early-onset atrial fibrillation in congenital long QT syndrome. Heart Rhythm 2008 5 5 704 709 2-s2.0-42649145054 10.1016/j.hrthm.2008.02.007
-
(2008)
Heart Rhythm
, vol.5
, Issue.5
, pp. 704-709
-
-
Johnson, J.N.1
Tester, D.J.2
Perry, J.3
Salisbury, B.A.4
Reed, C.R.5
Ackerman, M.J.6
-
35
-
-
34548383412
-
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: Do we need a scoring system?
-
DOI 10.1093/eurheartj/ehl355
-
Hofman N., Wilde A. A. M., Kääb S., van Langen I. M., Tanck M. W. T., Mannens M. M. A. M., Hinterseer M., Beckmann B. M., Tan H. L., Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European Heart Journal 2007 28 5 575 580 2-s2.0-34548383412 10.1093/eurheartj/ehl355 (Pubitemid 47355496)
-
(2007)
European Heart Journal
, vol.28
, Issue.5
, pp. 575-580
-
-
Hofman, N.1
Wilde, A.A.M.2
Kaab, S.3
Van Langen, I.M.4
Tanck, M.W.T.5
Mannens, M.M.A.M.6
Hinterseer, M.7
Beckmann, B.-M.8
Tan, H.L.9
-
36
-
-
20344388309
-
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: Characteristic T-U-wave patterns predict the KCNJ2 genotype
-
DOI 10.1161/CIRCULATIONAHA.104.472498
-
Zhang L., Benson D. W., Tristani-Firouzi M., Ptacek L. J., Tawil R., Schwartz P. J., George A. L., Horie M., Andelfinger G., Snow G. L., Fu Y. H., Ackerman M. J., Vincent G. M., Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype. Circulation 2005 111 21 2720 2726 2-s2.0-20344388309 10.1161/CIRCULATIONAHA.104.472498 (Pubitemid 40791541)
-
(2005)
Circulation
, vol.111
, Issue.21
, pp. 2720-2726
-
-
Zhang, L.1
Benson, D.W.2
Tristani-Firouzi, M.3
Ptacek, 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
-
37
-
-
17044446589
-
Effectiveness and limitations of β-blocker therapy in congenital long- QT syndrome
-
Moss A. J., Zareba W., Hall W. J., Schwartz P. J., Crampton R. S., Benhorin J., Vincent G. M., Locati E. H., Priori S. G., Napolitano C., Medina A., Zhang L., Robinson J. L., Timothy K., Towbin J. A., Andrews M. L., Effectiveness and limitations of β -blocker therapy in congenital long- QT syndrome. Circulation 2000 101 6 616 623 2-s2.0-17044446589 (Pubitemid 30094732)
-
(2000)
Circulation
, vol.101
, Issue.6
, pp. 616-623
-
-
Moss, A.J.1
Zareba, W.2
Hall, W.J.3
Schwartz, P.J.4
Crampton, R.S.5
Benhorin, J.6
Vincent, G.M.7
Locati, E.H.8
Priori, S.G.9
Napolitano, C.10
Medina, A.11
Zhang, L.12
Robinson, J.L.13
Timothy, K.14
Towbin, J.A.15
Andrews, M.L.16
-
38
-
-
0034730085
-
The elusive link between LQT3 and brugada syndrome: The role of flecainide challenge
-
Priori S. G., Napolitano C., Schwartz P. J., Bloise R., Crotti L., Ronchetti E., The elusive link between LQT3 and brugada syndrome: the role of flecainide challenge. Circulation 2000 102 9 945 947 2-s2.0-0034730085 (Pubitemid 30656000)
-
(2000)
Circulation
, vol.102
, Issue.9
, pp. 945-947
-
-
Priori, S.G.1
Napolitano, C.2
Schwartz, P.J.3
Bloise, R.4
Crotti, L.5
Ronchetti, E.6
-
39
-
-
0028842251
-
A new form of long QT syndrome associated with syndactyly
-
2-s2.0-0028842251 10.1016/0735-1097(94)00318-K
-
Marks M. L., Whisler S. L., Clericuzio C., Keating M., A new form of long QT syndrome associated with syndactyly. Journal of the American College of Cardiology 1995 25 1 59 64 2-s2.0-0028842251 10.1016/0735-1097(94)00318-K
-
(1995)
Journal of the American College of Cardiology
, vol.25
, Issue.1
, pp. 59-64
-
-
Marks, M.L.1
Whisler, S.L.2
Clericuzio, C.3
Keating, M.4
-
40
-
-
0026847447
-
The heart-hand syndrome: A new variant of disorders of heart conduction and syndactylia including osseous changes in hands and feet
-
2-s2.0-0026847447
-
Reichenbach H., Meister E. M., Theile H., The heart-hand syndrome: a new variant of disorders of heart conduction and syndactylia including osseous changes in hands and feet. Kinderarztliche Praxis 1992 60 2 54 56 2-s2.0-0026847447
-
(1992)
Kinderarztliche Praxis
, vol.60
, Issue.2
, pp. 54-56
-
-
Reichenbach, H.1
Meister, E.M.2
Theile, H.3
-
41
-
-
5344223383
-
V1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
-
DOI 10.1016/j.cell.2004.09.011, PII S0092867404008426
-
Splawski I., Timothy K. W., Sharpe L. M., Decher N., Kumar P., Bloise R., Napolitano C., Schwartz P. J., Joseph R. M., Condouris K., Tager-Flusberg H., Priori S. G., Sanguinetti M. C., Keating M. T., CaV1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Cell 2004 119 1 19 31 2-s2.0-5344223383 10.1016/j.cell.2004.09.011 (Pubitemid 39349317)
-
(2004)
Cell
, vol.119
, Issue.1
, pp. 19-31
-
-
Splawski, I.1
Timothy, K.W.2
Sharpe, L.M.3
Decher, N.4
Kumar, P.5
Bloise, R.6
Napolitano, C.7
Schwartz, P.J.8
Joseph, R.M.9
Condouris, K.10
Tager-Flusberg, H.11
Priori, S.G.12
Sanguinetti, M.C.13
Keating, M.T.14
|