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Items: 1 to 20 of 142

1.

GenTAC registry report: gender differences among individuals with genetically triggered thoracic aortic aneurysm and dissection.

Holmes KW, Maslen CL, Kindem M, Kroner BL, Song HK, Ravekes W, Dietz HC, Weinsaft JW, Roman MJ, Devereux RB, Pyeritz RE, Bavaria J, Milewski K, Milewicz D, LeMaire SA, Hendershot T, Eagle KA, Tolunay HE, Desvigne-Nickens P, Silberbach M; GenTAC Registry Consortium.

Am J Med Genet A. 2013 Apr;161A(4):779-86. doi: 10.1002/ajmg.a.35836. Epub 2013 Feb 26.

2.

Endovascular therapy in patients with genetically triggered thoracic aortic disease: applications and short- and mid-term outcomes.

Preventza O, Mohammed S, Cheong BY, Gonzalez L, Ouzounian M, Livesay JJ, Cooley DA, Coselli JS.

Eur J Cardiothorac Surg. 2014 Aug;46(2):248-53; discussion 253. doi: 10.1093/ejcts/ezt636. Epub 2014 Jan 28.

PMID:
24477738
3.

Surgical treatment of patients enrolled in the national registry of genetically triggered thoracic aortic conditions.

Song HK, Bavaria JE, Kindem MW, Holmes KW, Milewicz DM, Maslen CL, Pyeritz RE, Basson CT, Eagle K, Tolunay HE, Kroner BL, Dietz H, Menashe V, Devereux RB, Desvigne-Nickens P, Ravekes W, Weinsaft JW, Brambilla D, Stylianou MP, Hendershot T, Mitchell MS, LeMaire SA; National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC) Consortium.

Ann Thorac Surg. 2009 Sep;88(3):781-7; discussion 787-8. doi: 10.1016/j.athoracsur.2009.04.034.

4.

Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections.

Prakash S, Kuang SQ; GenTAC Registry Investigators, Regalado E, Guo D, Milewicz D.

PLoS One. 2016 Apr 19;11(4):e0153543. doi: 10.1371/journal.pone.0153543. eCollection 2016.

5.

Long-term implications of emergency versus elective proximal aortic surgery in patients with Marfan syndrome in the Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium Registry.

Song HK, Kindem M, Bavaria JE, Dietz HC, Milewicz DM, Devereux RB, Eagle KA, Maslen CL, Kroner BL, Pyeritz RE, Holmes KW, Weinsaft JW, Menashe V, Ravekes W, LeMaire SA; Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium.

J Thorac Cardiovasc Surg. 2012 Feb;143(2):282-6. doi: 10.1016/j.jtcvs.2011.10.024. Epub 2011 Nov 20.

6.

Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.

Hasham SN, Willing MC, Guo DC, Muilenburg A, He R, Tran VT, Scherer SE, Shete SS, Milewicz DM.

Circulation. 2003 Jul 1;107(25):3184-90. Epub 2003 Jun 23.

7.

Familial thoracic aortic aneurysms and dissections--incidence, modes of inheritance, and phenotypic patterns.

Albornoz G, Coady MA, Roberts M, Davies RR, Tranquilli M, Rizzo JA, Elefteriades JA.

Ann Thorac Surg. 2006 Oct;82(4):1400-5.

PMID:
16996941
8.

Histological and genetic studies in patients with bicuspid aortic valve and ascending aorta complications.

Pisano C, Maresi E, Balistreri CR, Candore G, Merlo D, Fattouch K, Bianco G, Ruvolo G.

Interact Cardiovasc Thorac Surg. 2012 Mar;14(3):300-6. doi: 10.1093/icvts/ivr114. Epub 2011 Dec 22.

9.

Thoracic aortic aneurysm and dissection.

Goldfinger JZ, Halperin JL, Marin ML, Stewart AS, Eagle KA, Fuster V.

J Am Coll Cardiol. 2014 Oct 21;64(16):1725-39. doi: 10.1016/j.jacc.2014.08.025. Review.

10.

FBN1 polymorphisms in patients with the dilatative pathology of the ascending thoracic aorta.

Lesauskaite V, Sepetiene R, Jariene G, Patamsyte V, Zukovas G, Grabauskyte I, Stanioniene Z, Sirmenis R, Benetis R.

Eur J Cardiothorac Surg. 2015 Apr;47(4):e124-30. doi: 10.1093/ejcts/ezu520. Epub 2015 Jan 12.

PMID:
25583878
11.

Nonsyndromic genetic predisposition to aortic dissection: a newly recognized, diagnosable, and preventable occurrence in families.

Hasham SN, Lewin MR, Tran VT, Pannu H, Muilenburg A, Willing M, Milewicz DM.

Ann Emerg Med. 2004 Jan;43(1):79-82.

PMID:
14707946
12.

The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): results from phase I and scientific opportunities in phase II.

Kroner BL, Tolunay HE, Basson CT, Pyeritz RE, Holmes KW, Maslen CL, Milewicz DM, LeMaire SA, Hendershot T, Desvigne-Nickens P, Devereux RB, Dietz HC, Song HK, Ringer D, Mitchell M, Weinsaft JW, Ravekes W, Menashe V, Eagle KA.

Am Heart J. 2011 Oct;162(4):627-632.e1. doi: 10.1016/j.ahj.2011.07.002.

13.

[Familial thoracic aortic aneurysms and dissections can be divided into three different main categories].

Hannuksela M, Stattin EL, Nyberg P, Carlberg B.

Lakartidningen. 2014 Feb 25;111(9-10):399-403. Review. Swedish.

PMID:
24570135
14.

Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection.

Guo DC, Regalado ES, Minn C, Tran-Fadulu V, Coney J, Cao J, Wang M, Yu RK, Estrera AL, Safi HJ, Shete SS, Milewicz DM.

Circ Cardiovasc Genet. 2011 Feb;4(1):36-42. doi: 10.1161/CIRCGENETICS.110.958066. Epub 2010 Dec 16.

15.

Characterizing the young patient with aortic dissection: results from the International Registry of Aortic Dissection (IRAD).

Januzzi JL, Isselbacher EM, Fattori R, Cooper JV, Smith DE, Fang J, Eagle KA, Mehta RH, Nienaber CA, Pape LA; International Registry of Aortic Dissection (IRAD).

J Am Coll Cardiol. 2004 Feb 18;43(4):665-9.

16.

Use of genetics for personalized management of heritable thoracic aortic disease: how do we get there?

Milewicz DM, Regalado ES.

J Thorac Cardiovasc Surg. 2015 Feb;149(2 Suppl):S3-5. doi: 10.1016/j.jtcvs.2014.07.070. Epub 2014 Aug 5. Review.

17.

Indications and imaging for aortic surgery: size and other matters.

Elefteriades JA, Ziganshin BA, Rizzo JA, Fang H, Tranquilli M, Paruchuri V, Kuzmik G, Gubernikoff G, Dumfarth J, Charilaou P, Theodoropoulos P.

J Thorac Cardiovasc Surg. 2015 Feb;149(2 Suppl):S10-3. doi: 10.1016/j.jtcvs.2014.07.066. Epub 2014 Aug 4.

PMID:
25218531
18.

Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms.

Regalado E, Medrek S, Tran-Fadulu V, Guo DC, Pannu H, Golabbakhsh H, Smart S, Chen JH, Shete S, Kim DH, Stern R, Braverman AC, Milewicz DM.

Am J Med Genet A. 2011 Sep;155A(9):2125-30. doi: 10.1002/ajmg.a.34050. Epub 2011 Aug 3.

19.

Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).

Roman MJ, Pugh NL, Hendershot TP, Devereux RB, Dietz H, Holmes K, Eagle KA, LeMaire SA, Milewicz DM, Morris SA, Pyeritz RE, Ravekes WJ, Shohet RV, Silberbach M; GenTAC InvestigatorsDietzHarry C.HabashiJenniferPrakashSiddharth K.MaslenCheryl L.SongHoward K.BavariaJoseph E.MilewskiKariannaWeinsaftJonathan W.McDonnellNazliAschFederico M.TolunayH. EserDesvigne‐NickensPatriceTsengHungKronerBarbara L.

J Am Heart Assoc. 2016 Aug 11;5(8). pii: e004052. doi: 10.1161/JAHA.116.004052.

20.

Marfan syndrome and the evolving spectrum of heritable thoracic aortic disease: do we need genetics for clinical decisions?

von Kodolitsch Y, Rybczynski M, Bernhardt A, Mir TS, Treede H, Dodge-Khatami A, Robinson PN, Sheikhzadeh S, Reichenspurner H, Meinertz T.

Vasa. 2010 Feb;39(1):17-32. doi: 10.1024/0301-1526/a000002. Review.

PMID:
20186673
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