Towbin JA - Search Results

1

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.

Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z. Moss AJ, et al. Among authors: towbin ja. Circulation. 2002 Feb 19;105(7):794-9. doi: 10.1161/hc0702.105124. Circulation. 2002. PMID: 11854117

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

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.

Jiang C, Atkinson D, Towbin JA, Splawski I, Lehmann MH, Li H, Timothy K, Taggart RT, Schwartz PJ, Vincent GM, et al. Jiang C, et al. Among authors: towbin ja. Nat Genet. 1994 Oct;8(2):141-7. doi: 10.1038/ng1094-141. Nat Genet. 1994. PMID: 7842012

4

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.

5

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

6

Evidence of genetic heterogeneity in the long QT syndrome.

Benhorin J, Kalman YM, Medina A, Towbin J, Rave-Harel N, Dyer TD, Blangero J, MacCluer JW, Kerem BS. Benhorin J, et al. Science. 1993 Jun 25;260(5116):1960-2. doi: 10.1126/science.8316839. Science. 1993. PMID: 8316839 No abstract available.

7

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantù F, Towbin JA, Keating MT, Hammoude H, Brown AM, Chen LS, Colatsky TJ. Schwartz PJ, et al. Among authors: towbin ja. Circulation. 1995 Dec 15;92(12):3381-6. doi: 10.1161/01.cir.92.12.3381. Circulation. 1995. PMID: 8521555

8

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

Roden DM, Lazzara R, Rosen M, Schwartz PJ, Towbin J, Vincent GM. Roden DM, et al. Circulation. 1996 Oct 15;94(8):1996-2012. doi: 10.1161/01.cir.94.8.1996. Circulation. 1996. PMID: 8873679 Review.

9

Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome.

Lehmann MH, Timothy KW, Frankovich D, Fromm BS, Keating M, Locati EH, Taggart RT, Towbin JA, Moss AJ, Schwartz PJ, Vincent GM. Lehmann MH, et al. Among authors: towbin ja. J Am Coll Cardiol. 1997 Jan;29(1):93-9. doi: 10.1016/s0735-1097(96)00454-8. J Am Coll Cardiol. 1997. PMID: 8996300 Free article.

10

Molecular genetics of long QT syndrome from genes to patients.

Wang Q, Chen Q, Li H, Towbin JA. Wang Q, et al. Among authors: towbin ja. Curr Opin Cardiol. 1997 May;12(3):310-20. doi: 10.1097/00001573-199705000-00013. Curr Opin Cardiol. 1997. PMID: 9243089 Review.

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