Bowles NE - Search Results

1

Towbin JA, Vatta M, Li H, Bowles NE. Towbin JA, et al. Among authors: bowles ne. Adv Pediatr. 2002;49:87-129. Adv Pediatr. 2002. PMID: 12214781 Review.

2

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA. Vatta M, et al. Among authors: bowles ne. Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337. Hum Mol Genet. 2002. PMID: 11823453

3

The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Bowles NE, Ni J, Marcus F, Towbin JA. Bowles NE, et al. J Am Coll Cardiol. 2002 Mar 6;39(5):892-5. doi: 10.1016/s0735-1097(02)01688-1. J Am Coll Cardiol. 2002. PMID: 11869858 Free article.

4

Arrhythmogenic inherited heart muscle diseases in children.

Towbin JA, Bowles NE. Towbin JA, et al. Among authors: bowles ne. J Electrocardiol. 2001;34 Suppl:151-65. doi: 10.1054/jelc.2001.28859. J Electrocardiol. 2001. PMID: 11781950 Review.

5

Molecular genetics of left ventricular dysfunction.

Towbin JA, Bowles NE. Towbin JA, et al. Among authors: bowles ne. Curr Mol Med. 2001 Mar;1(1):81-90. doi: 10.2174/1566524013364077. Curr Mol Med. 2001. PMID: 11899244 Review.

6

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: bowles ne. Mol Genet Metab. 2002 Apr;75(4):308-16. doi: 10.1016/S1096-7192(02)00007-0. Mol Genet Metab. 2002. PMID: 12051962

7

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Among authors: bowles ne. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963

8

Molecular diagnosis of myocardial disease.

Towbin JA, Bowles NE. Towbin JA, et al. Among authors: bowles ne. Expert Rev Mol Diagn. 2002 Nov;2(6):587-602. doi: 10.1586/14737159.2.6.587. Expert Rev Mol Diagn. 2002. PMID: 12465455 Review.

9

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction.

Vatta M, Mohapatra B, Jimenez S, Sanchez X, Faulkner G, Perles Z, Sinagra G, Lin JH, Vu TM, Zhou Q, Bowles KR, Di Lenarda A, Schimmenti L, Fox M, Chrisco MA, Murphy RT, McKenna W, Elliott P, Bowles NE, Chen J, Valle G, Towbin JA. Vatta M, et al. Among authors: bowles kr, bowles ne. J Am Coll Cardiol. 2003 Dec 3;42(11):2014-27. doi: 10.1016/j.jacc.2003.10.021. J Am Coll Cardiol. 2003. PMID: 14662268 Free article.

10

Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devices.

Vatta M, Stetson SJ, Jimenez S, Entman ML, Noon GP, Bowles NE, Towbin JA, Torre-Amione G. Vatta M, et al. Among authors: bowles ne. J Am Coll Cardiol. 2004 Mar 3;43(5):811-7. doi: 10.1016/j.jacc.2003.09.052. J Am Coll Cardiol. 2004. PMID: 14998622 Free article.

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