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Items: 1 to 20 of 102

1.

New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections.

Campens L, Renard M, Callewaert B, Coucke P, De Backer J, De Paepe A.

Pol Arch Med Wewn. 2013;123(12):693-700. Review.

2.

Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice.

De Backer J, Renard M, Campens L, François K, Callewaert B, Coucke P, De Paepe A.

Aorta (Stamford). 2013 Jul 1;1(2):135-45. doi: 10.12945/j.aorta.2013.13-024.

3.

Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.

De Backer J, Renard M, Campens L, Mosquera LM, De Paepe A, Coucke P, Callewaert B, Kodolitsch Yv.

Curr Pharm Des. 2015;21(28):4061-75. Review.

PMID:
26306841
4.

The genetic message of a sudden, unexpected death due to thoracic aortic dissection.

Ripperger T, Tröger HD, Schmidtke J.

Forensic Sci Int. 2009 May 30;187(1-3):1-5. doi: 10.1016/j.forsciint.2009.01.020.

PMID:
19285815
5.

Exon 47 skipping of fibrillin-1 leads preferentially to cardiovascular defects in patients with thoracic aortic aneurysms and dissections.

Wang WJ, Han P, Zheng J, Hu FY, Zhu Y, Xie JS, Guo J, Zhang Z, Dong J, Zheng GY, Cao H, Liu TS, Fu Q, Sun L, Yang BB, Tian XL.

J Mol Med (Berl). 2013 Jan;91(1):37-47. doi: 10.1007/s00109-012-0931-y.

PMID:
22772377
6.

Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?

Waldmüller S, Müller M, Warnecke H, Rees W, Schöls W, Walterbusch G, Ennker J, Scheffold T.

Eur J Cardiothorac Surg. 2007 Jun;31(6):970-5.

PMID:
17418587
7.

FBN1 mutations in patients with descending thoracic aortic dissections.

Brautbar A, LeMaire SA, Franco LM, Coselli JS, Milewicz DM, Belmont JW.

Am J Med Genet A. 2010 Feb;152A(2):413-6. doi: 10.1002/ajmg.a.32856.

8.

The molecular genetics of Marfan syndrome and related disorders.

Robinson PN, Arteaga-Solis E, Baldock C, Collod-Béroud G, Booms P, De Paepe A, Dietz HC, Guo G, Handford PA, Judge DP, Kielty CM, Loeys B, Milewicz DM, Ney A, Ramirez F, Reinhardt DP, Tiedemann K, Whiteman P, Godfrey M.

J Med Genet. 2006 Oct;43(10):769-87. Review.

9.

The non-syndromic familial thoracic aortic aneurysms and dissections maps to 15q21 locus.

Keramati AR, Sadeghpour A, Farahani MM, Chandok G, Mani A.

BMC Med Genet. 2010 Oct 11;11:143. doi: 10.1186/1471-2350-11-143.

10.

Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations.

Teekakirikul P, Milewicz DM, Miller DT, Lacro RV, Regalado ES, Rosales AM, Ryan DP, Toler TL, Lin AE.

Am J Med Genet A. 2013 Jan;161A(1):185-91. doi: 10.1002/ajmg.a.35659.

11.

Genetic variants in FBN-1 and risk for thoracic aortic aneurysm and dissection.

Iakoubova OA, Tong CH, Rowland CM, Luke MM, Garcia VE, Catanese JJ, Moomiaie RM, Sotonyi P, Ascady G, Nikas D, Dedelias P, Tranquilli M, Elefteriades JA.

PLoS One. 2014 Apr 17;9(4):e91437. doi: 10.1371/journal.pone.0091437.

12.

The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys-Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD).

Lerner-Ellis JP, Aldubayan SH, Hernandez AL, Kelly MA, Stuenkel AJ, Walsh J, Joshi VA.

Mol Genet Metab. 2014 Jun;112(2):171-6. doi: 10.1016/j.ymgme.2014.03.011.

PMID:
24793577
13.

Actual management of patients with familial ascending aortic aneurysms and type-A aortic dissections.

Weigang E, Chang XC, Munk-Schulenburg S, Richter H, von Samson P, Goebel H, Frydrychowicz A, Geibel A, Ammann S, Schwering L, Brunner T, Severin T, Czerny M, Beyersdorf F.

Thorac Cardiovasc Surg. 2007 Feb;55(1):19-23.

PMID:
17285469
14.

Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.

Mátyás G, Arnold E, Carrel T, Baumgartner D, Boileau C, Berger W, Steinmann B.

Hum Mutat. 2006 Aug;27(8):760-9.

PMID:
16791849
15.

Heritable diseases of the blood vessels.

Baxter BT.

Cardiovasc Pathol. 2005 Jul-Aug;14(4):185-8. Review.

PMID:
16009316
16.

Smad2-dependent protease nexin-1 overexpression differentiates chronic aneurysms from acute dissections of human ascending aorta.

Gomez D, Kessler K, Borges LF, Richard B, Touat Z, Ollivier V, Mansilla S, Bouton MC, Alkoder S, Nataf P, Jandrot-Perrus M, Jondeau G, Vranckx R, Michel JB.

Arterioscler Thromb Vasc Biol. 2013 Sep;33(9):2222-32. doi: 10.1161/ATVBAHA.113.301327.

17.

Marfan syndrome: from gene to therapy.

Bolar N, Van Laer L, Loeys BL.

Curr Opin Pediatr. 2012 Aug;24(4):498-504. doi: 10.1097/MOP.0b013e3283557d4c. Review.

PMID:
22705998
18.

Inherited diseases and syndromes leading to aortic aneurysms and dissections.

Caglayan AO, Dundar M.

Eur J Cardiothorac Surg. 2009 Jun;35(6):931-40. doi: 10.1016/j.ejcts.2009.01.006. Review.

PMID:
19233667
19.

Familial thoracic aortic aneurysm and dissection associated with Marfan-related gene mutations: case report of a family with two gene mutations.

Yamawaki T, Nagaoka K, Morishige K, Sadamatsu K, Tashiro H, Yasunaga H, Morisaki H, Morisaki T.

Intern Med. 2009;48(7):555-8.

20.

The pathogenesis of aortopathy in Marfan syndrome and related diseases.

Jones JA, Ikonomidis JS.

Curr Cardiol Rep. 2010 Mar;12(2):99-107. doi: 10.1007/s11886-010-0083-z. Review.

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