|1.||Milewicz, Dianna M: 19 articles (12/2014 - 07/2003)|
|2.||Guo, Dong-Chuan: 10 articles (12/2014 - 12/2007)|
|3.||Regalado, Ellen S: 8 articles (02/2014 - 05/2009)|
|4.||Estrera, Anthony L: 8 articles (10/2011 - 07/2005)|
|5.||Safi, Hazim J: 8 articles (10/2011 - 07/2005)|
|6.||Tran-Fadulu, Van: 8 articles (09/2011 - 11/2005)|
|7.||Pannu, Hariyadarshi: 8 articles (09/2011 - 07/2005)|
|8.||LeMaire, Scott A: 6 articles (04/2013 - 05/2009)|
|9.||Coselli, Joseph S: 5 articles (05/2012 - 05/2009)|
|10.||Zheng, Jun: 4 articles (08/2015 - 01/2013)|
|2.||Aortic Aneurysm (Aneurysm, Aortic)
06/01/2011 - "In this study, we investigated the association of recurrent genomic copy number variants (CNVs) with thoracic aortic aneurysms and dissections (TAAD). "
08/04/2015 - "Point mutations in vascular smooth muscle α-actin (SM α-actin), encoded by the gene ACTA2, are the most prevalent cause of familial thoracic aortic aneurysms and dissections (TAAD). "
03/01/2015 - "Non-syndromic familial thoracic aortic aneurysms and dissections (TAAD) are inherited in an autosomal dominant manner. "
02/26/2014 - "Thoracic aortic aneurysms and dissections (TAAD) can be divided into three different main categories. "
02/01/2014 - "Approximately 20% of patients with thoracic aortic aneurysms and dissections (TAAD) have a family history of the disease, referred to as familial TAAD (FTAAD) that can be inherited in an autosomal dominant manner with variable expression with respect to disease presentation, age of onset and associated features. "
|3.||Thoracic Aortic Aneurysm
11/01/2014 - "This study aimed at exploring the causative gene and summarizing the clinical characteristics in a Chinese thoracic aortic aneurysm and dissection (TAAD) family. "
11/01/2015 - "Hereditary factors play an important etiologic role in thoracic aortic aneurysm and dissection (TAAD), with a number of genes proven to predispose to this condition. "
12/04/2014 - "Thoracic aortic aneurysm and dissection (TAAD) is an autosomal-dominant disorder with major life-threatening complications. "
07/01/2014 - "Hybrid repair (HR) of thoracoabdominal aortic aneurysm (TAAA) and dissection (TAAD), consisting of rerouting renovisceral branches followed by endograft aortic repair, has been shown to be a feasible option. "
01/01/2014 - "A recent genome wide association study (GWAS) by LeMaire et al. found that two single nucleotide polymorphisms (SNPs), rs2118181 and rs10519177 in the FBN-1 gene (encoding Fibrillin-1), were associated with thoracic aortic dissection (TAD), non-dissecting thoracic aortic aneurysm (TAA), and thoracic aortic aneurysm or dissection (TAAD); the largest effect was observed for the association of rs2118181 with TAD. "
|4.||Marfan Syndrome (Marfan's Syndrome)
10/01/2011 - "FBN1 mutations cause Marfan syndrome, whose major cardiovascular complication is TAAD. "
05/01/2011 - "In order to further explore the role of ACTA2 variations in the pathogenesis of TAAD, we sequenced the coding regions of this gene in 40 unrelated German patients with TAAD (with (n=21) or without (n=19) clinical features suggestive of Marfan syndrome). "
01/01/2010 - "In addition, association of non-syndromic TAAD with the Marfan disease gene locus poses the question whether secondary prevention strategies employed for Marfan syndrome patients should be applied to all patients with familial TAAD."
07/26/2005 - "We found TGFBR2 mutations in 4 unrelated families with familial TAAD who did not have Marfan syndrome. "
04/01/2013 - "We performed cross-sectional analyses in adults with Marfan syndrome (MFS), familial thoracic aortic aneurysm or dissection (FTAAD), bicuspid aortic valve (BAV) with thoracic aortic aneurysm or dissection, and subjects under 50 years of age with thoracic aortic aneurysm or dissection (TAAD <50 years). "
06/01/2014 - "In this study, patients suspected of having a clinical diagnosis of Marfan Syndrome (MFS), Loeys-Dietz Syndrome (LDS) and Thoracic Aortic Aneurysms and Dissections (TAAD) were referred for genetic testing and examined for mutations in the FBN1, TGFβR1, TGFβR2 and ACTA2 genes. "
06/01/2014 - "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)."
02/26/2014 - "1. Inherited syndromes predisposing to TAAD such as Marfan syndrome, Ehlers-Danlos syndrome type IV and Loeys-Dietz syndrome (less than 5% of all TAAD). "
01/01/2008 - "Thoracic aortic aneurysms leading to type A dissections (TAAD) can be inherited in isolation or in association with genetic syndromes, such as Marfan syndrome and Loeys-Dietz syndrome. "
11/01/2014 - "Total serum transforming growth factor-beta 1 (tsTGF-β1) is increased in patients with Marfan syndrome (MFS), but it has not been assessed in thoracic aortic aneurysm and dissection (TAAD), Loeys-Dietz syndrome (LDS), and bicuspid aortic valve disease (BAVD). "
|1.||Actins (F Actin)
|2.||Myosin Heavy Chains (Myosin Heavy Chain)
|3.||Transforming Growth Factor beta Receptors (TGF beta Receptors)
|4.||Transforming Growth Factor beta (TGF-beta)
|5.||Marfan Syndrome type 2
|6.||DNA (Deoxyribonucleic Acid)
|3.||Hydrocolloid Bandages (Duoderm)