Moss AJ - Search Results

1

Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.

Wang Z, Li H, Moss AJ, Robinson J, Zareba W, Knilans T, Bowles NE, Towbin JA. Wang Z, et al. Among authors: moss aj. Mol Genet Metab. 2002 Apr;75(4):308-16. doi: 10.1016/S1096-7192(02)00007-0. Mol Genet Metab. 2002. PMID: 12051962

2

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: moss aj. Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264. Circulation. 1998. PMID: 9570196

3

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

4

Novel compound heterozygous mutations in the KCNQ1 gene associated with autosomal recessive long QT syndrome (Jervell and Lange-Nielsen syndrome).

Ning L, Moss AJ, Zareba W, Robinson J, Rosero S, Ryan D, Qi M. Ning L, et al. Among authors: moss aj. Ann Noninvasive Electrocardiol. 2003 Jul;8(3):246-50. doi: 10.1046/j.1542-474x.2003.08313.x. Ann Noninvasive Electrocardiol. 2003. PMID: 14510661 Free PMC article.

5

Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome.

Goldenberg I, Moss AJ, Zareba W, McNitt S, Robinson JL, Qi M, Towbin JA, Ackerman MJ, Murphy L. Goldenberg I, et al. Among authors: moss aj. J Cardiovasc Electrophysiol. 2006 Nov;17(11):1161-8. doi: 10.1111/j.1540-8167.2006.00587.x. Epub 2006 Aug 14. J Cardiovasc Electrophysiol. 2006. PMID: 16911578

6

Genotype-phenotype aspects of type 2 long QT syndrome.

Shimizu W, Moss AJ, Wilde AA, Towbin JA, Ackerman MJ, January CT, Tester DJ, Zareba W, Robinson JL, Qi M, Vincent GM, Kaufman ES, Hofman N, Noda T, Kamakura S, Miyamoto Y, Shah S, Amin V, Goldenberg I, Andrews ML, McNitt S. Shimizu W, et al. Among authors: moss aj. J Am Coll Cardiol. 2009 Nov 24;54(22):2052-62. doi: 10.1016/j.jacc.2009.08.028. J Am Coll Cardiol. 2009. PMID: 19926013 Free PMC 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. Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635. Circulation. 1994. PMID: 7994803

8

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

9

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, Schwartz PJ, Vincent GM, Priori SG, Benhorin J, Towbin JA, Robinson JL, Andrews ML, Napolitano C, Timothy K, Zhang L, Medina A; International Long QT Syndrome Registry. Zareba W, et al. Among authors: moss aj. J Am Coll Cardiol. 2003 Jul 2;42(1):103-9. doi: 10.1016/s0735-1097(03)00554-0. J Am Coll Cardiol. 2003. PMID: 12849668 Free article.

10

Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation.

Horr S, Goldenberg I, Moss AJ, O-Uchi J, Barsheshet A, Connelly H, Gray DA, Zareba W, Lopes CM. Horr S, et al. Among authors: moss aj. J Cardiovasc Electrophysiol. 2011 Feb;22(2):193-200. doi: 10.1111/j.1540-8167.2010.01852.x. J Cardiovasc Electrophysiol. 2011. PMID: 20662986 Free PMC article.

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