Robinson JL - Search Results

1

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.

Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT. Splawski I, et al. Among authors: robinson jl. Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178. Circulation. 2000. PMID: 10973849

2

Clinical features of the idiopathic long QT syndrome.

Moss AJ, Robinson J. Moss AJ, et al. Circulation. 1992 Jan;85(1 Suppl):I140-4. Circulation. 1992. PMID: 1345816 Review.

3

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

4

Efficacy of permanent pacing in the management of high-risk patients with long QT syndrome.

Moss AJ, Liu JE, Gottlieb S, Locati EH, Schwartz PJ, Robinson JL. Moss AJ, et al. Among authors: robinson jl. Circulation. 1991 Oct;84(4):1524-9. doi: 10.1161/01.cir.84.4.1524. Circulation. 1991. PMID: 1914094

5

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: robinson jl. Circulation. 1995 Nov 15;92(10):2929-34. doi: 10.1161/01.cir.92.10.2929. Circulation. 1995. PMID: 7586261

6

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: robinson jl. Cell. 1995 Mar 10;80(5):805-11. doi: 10.1016/0092-8674(95)90359-3. Cell. 1995. PMID: 7889574 Free article.

7

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. Among authors: robinson jl. Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635. Circulation. 1994. PMID: 7994803

8

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: robinson jl. Circulation. 1998 Jun 9;97(22):2237-44. doi: 10.1161/01.cir.97.22.2237. Circulation. 1998. PMID: 9631873

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: robinson jl. Circulation. 1999 Mar 16;99(10):1344-7. doi: 10.1161/01.cir.99.10.1344. Circulation. 1999. PMID: 10077519

10

Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

Moss AJ, Zareba W, Hall WJ, Schwartz PJ, Crampton RS, Benhorin J, Vincent GM, Locati EH, Priori SG, Napolitano C, Medina A, Zhang L, Robinson JL, Timothy K, Towbin JA, Andrews ML. Moss AJ, et al. Among authors: robinson jl. Circulation. 2000 Feb 15;101(6):616-23. doi: 10.1161/01.cir.101.6.616. Circulation. 2000. PMID: 10673253 Clinical Trial.

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