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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
1997 | 1 |
1998 | 2 |
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2024 | 0 |
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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178.
Circulation. 2000.
PMID: 10973849
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H, Chen Q, Moss AJ, Robinson J, Goytia V, Perry JC, Vincent GM, Priori SG, Lehmann MH, Denfield SW, Duff D, Kaine S, Shimizu W, Schwartz PJ, Wang Q, Towbin JA.
Li H, et al.
Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264.
Circulation. 1998.
PMID: 9570196
Item in Clipboard
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.
Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA.
Chen Q, et al.
Circulation. 1999 Mar 16;99(10):1344-7. doi: 10.1161/01.cir.99.10.1344.
Circulation. 1999.
PMID: 10077519
Item in Clipboard
ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
Moss AJ, Zareba W, Benhorin J, Locati EH, Hall WJ, Robinson JL, Schwartz PJ, Towbin JA, Vincent GM, Lehmann MH.
Moss AJ, et al.
Circulation. 1995 Nov 15;92(10):2929-34. doi: 10.1161/01.cir.92.10.2929.
Circulation. 1995.
PMID: 7586261
Item in Clipboard
Clinical management of patients with the long QT syndrome: drugs, devices, and gene-specific therapy.
Moss AJ.
Moss AJ.
Pacing Clin Electrophysiol. 1997 Aug;20(8 Pt 2):2058-60. doi: 10.1111/j.1540-8159.1997.tb03627.x.
Pacing Clin Electrophysiol. 1997.
PMID: 9272508
Review.
Item in Clipboard
Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome. LQTS Investigators.
Rashba EJ, Zareba W, Moss AJ, Hall WJ, Robinson J, Locati EH, Schwartz PJ, Andrews M.
Rashba EJ, et al.
Circulation. 1998 Feb 10;97(5):451-6. doi: 10.1161/01.cir.97.5.451.
Circulation. 1998.
PMID: 9490239
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