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Items: 14

1.

Cardiac Arrhythmia After Open Thoracoabdominal Aortic Aneurysm Repair.

Dolapoglu A, Volguina IV, Price MD, Green SY, Coselli JS, LeMaire SA.

Ann Thorac Surg. 2017 Apr 19. pii: S0003-4975(17)30191-1. doi: 10.1016/j.athoracsur.2017.01.077. [Epub ahead of print]

PMID:
28433218
2.

Results of Open Surgical Repair in Patients With Marfan Syndrome and Distal Aortic Dissection.

Coselli JS, Green SY, Price MD, Hash JA, Ouyang Y, Volguina IV, Preventza O, de la Cruz KI, LeMaire SA.

Ann Thorac Surg. 2016 Jun;101(6):2193-201. doi: 10.1016/j.athoracsur.2015.11.008. Epub 2016 Feb 12.

PMID:
26876340
3.

A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome.

Doyle JJ, Doyle AJ, Wilson NK, Habashi JP, Bedja D, Whitworth RE, Lindsay ME, Schoenhoff F, Myers L, Huso N, Bachir S, Squires O, Rusholme B, Ehsan H, Huso D, Thomas CJ, Caulfield MJ, Van Eyk JE, Judge DP, Dietz HC; GenTAC Registry Consortium.; MIBAVA Leducq Consortium..

Elife. 2015 Oct 27;4. pii: e08648. doi: 10.7554/eLife.08648.

4.

Early and 1-year outcomes of aortic root surgery in patients with Marfan syndrome: a prospective, multicenter, comparative study.

Coselli JS, Volguina IV, LeMaire SA, Sundt TM, Connolly HM, Stephens EH, Schaff HV, Milewicz DM, Vricella LA, Dietz HC, Minard CG, Miller DC; Aortic Valve Operative Outcomes in Marfan Patients Study Group..

J Thorac Cardiovasc Surg. 2014 Jun;147(6):1758-66, 1767.e1-4. doi: 10.1016/j.jtcvs.2014.02.021. Epub 2014 Feb 8.

5.

Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome.

Cook JR, Carta L, Bénard L, Chemaly ER, Chiu E, Rao SK, Hampton TG, Yurchenco P; GenTAC Registry Consortium., Costa KD, Hajjar RJ, Ramirez F.

J Clin Invest. 2014 Mar;124(3):1329-39. doi: 10.1172/JCI71059. Epub 2014 Feb 17.

6.

Mitral valve disease in patients with Marfan syndrome undergoing aortic root replacement.

Kunkala MR, Schaff HV, Li Z, Volguina I, Dietz HC, LeMaire SA, Coselli JS, Connolly H.

Circulation. 2013 Sep 10;128(11 Suppl 1):S243-7. doi: 10.1161/CIRCULATIONAHA.112.000113. Erratum in: Circulation. 2014 Mar 11;129(10):e390.

7.

Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.

Guo DC, Regalado E, Casteel DE, Santos-Cortez RL, Gong L, Kim JJ, Dyack S, Horne SG, Chang G, Jondeau G, Boileau C, Coselli JS, Li Z, Leal SM, Shendure J, Rieder MJ, Bamshad MJ, Nickerson DA; GenTAC Registry Consortium.; National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project., Kim C, Milewicz DM.

Am J Hum Genet. 2013 Aug 8;93(2):398-404. doi: 10.1016/j.ajhg.2013.06.019. Epub 2013 Aug 1.

8.

Single-nucleotide polymorphism array genotyping is equivalent to metaphase cytogenetics for diagnosis of Turner syndrome.

Prakash S, Guo D, Maslen CL, Silberbach M, Milewicz D, Bondy CA; GenTAC Investigators..

Genet Med. 2014 Jan;16(1):53-9. doi: 10.1038/gim.2013.77. Epub 2013 Jun 6. Erratum in: Genet Med. 2014 Jan;16(1):117.

9.

Intraoperative conversion after surgical failure: an overlooked complication of aortic root replacement in Marfan patients?

Volguina IV, LeMaire SA, Palmero LC, Miller DC, Coselli JS.

Tex Heart Inst J. 2011;38(6):684-6. No abstract available.

10.

Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.

Kuang SQ, Guo DC, Prakash SK, McDonald ML, Johnson RJ, Wang M, Regalado ES, Russell L, Cao JM, Kwartler C, Fraivillig K, Coselli JS, Safi HJ, Estrera AL, Leal SM, LeMaire SA, Belmont JW, Milewicz DM; GenTAC Investigators..

PLoS Genet. 2011 Jun;7(6):e1002118. doi: 10.1371/journal.pgen.1002118. Epub 2011 Jun 16.

11.

Valve-sparing and valve-replacing techniques for aortic root replacement in patients with Marfan syndrome: Analysis of early outcome.

Volguina IV, Miller DC, LeMaire SA, Palmero LC, Wang XL, Connolly HM, Sundt TM 3rd, Bavaria JE, Dietz HC, Milewicz DM, Coselli JS; Aortic Valve Operative Outcomes in Marfan Patients study group..

J Thorac Cardiovasc Surg. 2009 May;137(5):1124-32. doi: 10.1016/j.jtcvs.2009.03.023.

12.

Valve-sparing and valve-replacing techniques for aortic root replacement in patients with Marfan syndrome: analysis of early outcome.

Volguina IV, Miller DC, LeMaire SA, Palmero LC, Wang XL, Connolly HM, Sundt TM 3rd, Bavaria JE, Dietz HC, Milewicz DM, Coselli JS; Aortic Valve Operative Outcomes in Marfan Patients study group..

J Thorac Cardiovasc Surg. 2009 Mar;137(3):641-9. doi: 10.1016/j.jtcvs.2008.11.030. Corrected and republished in: J Thorac Cardiovasc Surg. 2009 May;137(5):1124-32.

13.

Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).

Eagle KA; GenTAC Consortium..

Am Heart J. 2009 Feb;157(2):319-26. doi: 10.1016/j.ahj.2008.10.005. Epub 2008 Dec 17.

14.

Spectrum of aortic operations in 300 patients with confirmed or suspected Marfan syndrome.

LeMaire SA, Carter SA, Volguina IV, Laux AT, Milewicz DM, Borsato GW, Cheung CK, Bozinovski J, Markesino JM, Vaughn WK, Coselli JS.

Ann Thorac Surg. 2006 Jun;81(6):2063-78; discussion 2078.

PMID:
16731131

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