Towbin JA - Search Results

1

Management of Congenital Long-QT Syndrome: Commentary From the Experts.

Kaufman ES, Eckhardt LL, Ackerman MJ, Aziz PF, Behr ER, Cerrone M, Chung MK, Cutler MJ, Etheridge SP, Krahn AD, Lubitz SA, Perez MV, Priori SG, Roberts JD, Roden DM, Schulze-Bahr E, Schwartz PJ, Shimizu W, Shoemaker MB, Sy RW, Towbin JA, Viskin S, A M Wilde A, Zareba W. Kaufman ES, et al. Among authors: towbin ja. Circ Arrhythm Electrophysiol. 2021 Jul;14(7):e009726. doi: 10.1161/CIRCEP.120.009726. Epub 2021 Jul 9. Circ Arrhythm Electrophysiol. 2021. PMID: 34238011 Free PMC article. Review.

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

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

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

6

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.

7

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.

8

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

9

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

10

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

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