Roberts R - Search Results

1

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy.

Gollob MH, Green MS, Tang AS, Roberts R. Gollob MH, et al. Among authors: roberts r. Curr Opin Cardiol. 2002 May;17(3):229-34. doi: 10.1097/00001573-200205000-00004. Curr Opin Cardiol. 2002. PMID: 12015471 Review.

2

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.

Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, Ahmad F, Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Gollob MH, et al. Among authors: roberts r. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. N Engl J Med. 2001. PMID: 11407343 Free article.

3

Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.

Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, Roberts R. Gollob MH, et al. Among authors: roberts r. Circulation. 2001 Dec 18;104(25):3030-3. doi: 10.1161/hc5001.102111. Circulation. 2001. PMID: 11748095

4

Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.

Sidhu JS, Rajawat YS, Rami TG, Gollob MH, Wang Z, Yuan R, Marian AJ, DeMayo FJ, Weilbacher D, Taffet GE, Davies JK, Carling D, Khoury DS, Roberts R. Sidhu JS, et al. Among authors: roberts r. Circulation. 2005 Jan 4;111(1):21-9. doi: 10.1161/01.CIR.0000151291.32974.D5. Epub 2004 Dec 20. Circulation. 2005. PMID: 15611370 Free PMC article.

5

Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen.

Folmes KD, Chan AY, Koonen DP, Pulinilkunnil TC, Baczkó I, Hunter BE, Thorn S, Allard MF, Roberts R, Gollob MH, Light PE, Dyck JR. Folmes KD, et al. Among authors: roberts r. Circ Cardiovasc Genet. 2009 Oct;2(5):457-66. doi: 10.1161/CIRCGENETICS.108.834564. Epub 2009 Jul 15. Circ Cardiovasc Genet. 2009. PMID: 20031621

6

AMP-activated protein kinase and familial Wolff-Parkinson-White syndrome: new perspectives on heart development and arrhythmogenesis.

Gollob MH, Roberts R. Gollob MH, et al. Among authors: roberts r. Eur Heart J. 2002 May;23(9):679-81. doi: 10.1053/euhj.2001.2954. Eur Heart J. 2002. PMID: 11977988 No abstract available.

7

Molecular cardiology and genetics in the 21st century--a primer.

Roberts R, Gollob M. Roberts R, et al. Curr Probl Cardiol. 2006 Oct;31(10):637-701. doi: 10.1016/j.cpcardiol.2006.05.004. Curr Probl Cardiol. 2006. PMID: 16962416 Review.

8

Relationship between pacemaker dependency and the effect of pacing mode on cardiovascular outcomes.

Tang AS, Roberts RS, Kerr C, Gillis AM, Green MS, Talajic M, Yusuf S, Abdollah H, Gent M, Connolly SJ. Tang AS, et al. Among authors: roberts rs. Circulation. 2001 Jun 26;103(25):3081-5. doi: 10.1161/01.cir.103.25.3081. Circulation. 2001. PMID: 11425772

9

Canadian Implantable Defibrillator Study (CIDS): study design and organization. CIDS Co-Investigators.

Connolly SJ, Gent M, Roberts RS, Dorian P, Green MS, Klein GJ, Mitchell LB, Sheldon RS, Roy D. Connolly SJ, et al. Among authors: roberts rs. Am J Cardiol. 1993 Nov 26;72(16):103F-108F. doi: 10.1016/0002-9149(93)90972-f. Am J Cardiol. 1993. PMID: 8237822 Clinical Trial.

10

Canadian implantable defibrillator study (CIDS) : a randomized trial of the implantable cardioverter defibrillator against amiodarone.

Connolly SJ, Gent M, Roberts RS, Dorian P, Roy D, Sheldon RS, Mitchell LB, Green MS, Klein GJ, O'Brien B. Connolly SJ, et al. Among authors: roberts rs. Circulation. 2000 Mar 21;101(11):1297-302. doi: 10.1161/01.cir.101.11.1297. Circulation. 2000. PMID: 10725290 Clinical Trial.

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