Towbin JA - Search Results

1

Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome.

Jons C, Moss AJ, Lopes CM, McNitt S, Zareba W, Goldenberg I, Qi M, Wilde AA, Shimizu W, Kanters JK, Towbin JA, Ackerman MJ, Robinson JL. Jons C, et al. Among authors: towbin ja. J Cardiovasc Electrophysiol. 2009 Aug;20(8):859-65. doi: 10.1111/j.1540-8167.2009.01455.x. Epub 2009 Mar 13. J Cardiovasc Electrophysiol. 2009. PMID: 19490272

2

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. Among authors: towbin ja. Circulation. 1995 Nov 15;92(10):2929-34. doi: 10.1161/01.cir.92.10.2929. Circulation. 1995. PMID: 7586261

3

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, Moss AJ, Towbin JA, Keating MT. Wang Q, et al. Among authors: towbin ja. Cell. 1995 Mar 10;80(5):805-11. doi: 10.1016/0092-8674(95)90359-3. Cell. 1995. PMID: 7889574 Free article.

4

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Towbin JA, Li H, Taggart RT, Lehmann MH, Schwartz PJ, Satler CA, Ayyagari R, Robinson JL, Moss A, Hejtmancik JF. Towbin JA, et al. Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635. Circulation. 1994. PMID: 7994803

5

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. Among authors: towbin ja. Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264. Circulation. 1998. PMID: 9570196

6

Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of congenital long-QT syndrome.

Shimizu W, Kurita T, Matsuo K, Suyama K, Aihara N, Kamakura S, Towbin JA, Shimomura K. Shimizu W, et al. Among authors: towbin ja. Circulation. 1998 Apr 28;97(16):1581-8. doi: 10.1161/01.cir.97.16.1581. Circulation. 1998. PMID: 9593563

7

Locati EH, Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Lehmann MH, Towbin JA, Priori SG, Napolitano C, Robinson JL, Andrews M, Timothy K, Hall WJ. Locati EH, et al. Among authors: towbin ja. Circulation. 1998 Jun 9;97(22):2237-44. doi: 10.1161/01.cir.97.22.2237. Circulation. 1998. PMID: 9631873

8

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Robinson JL, Priori SG, Benhorin J, Locati EH, Towbin JA, Keating MT, Lehmann MH, Hall WJ. Zareba W, et al. Among authors: towbin ja. N Engl J Med. 1998 Oct 1;339(14):960-5. doi: 10.1056/NEJM199810013391404. N Engl J Med. 1998. PMID: 9753711 Free article.

9

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. Among authors: towbin ja. Circulation. 1999 Mar 16;99(10):1344-7. doi: 10.1161/01.cir.99.10.1344. Circulation. 1999. PMID: 10077519

10

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.

Moss AJ, Robinson JL, Gessman L, Gillespie R, Zareba W, Schwartz PJ, Vincent GM, Benhorin J, Heilbron EL, Towbin JA, Priori SG, Napolitano C, Zhang L, Medina A, Andrews ML, Timothy K. Moss AJ, et al. Among authors: towbin ja. Am J Cardiol. 1999 Oct 15;84(8):876-9. doi: 10.1016/s0002-9149(99)00458-0. Am J Cardiol. 1999. PMID: 10532503 Free article.

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