Recurrent Aortic Dissection: Observations From the International Registry of Aortic Dissection
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Marc P. Bonaca | K. Eagle | E. Isselbacher | C. Nienaber | G. Jondeau | R. Pyeritz | M. Lindsay | U. Sechtem | H. Eckstein | J. Froehlich | H. Patel | A. Khoynezhad | M. Di Eusanio | D. Montgomery | F. Ramponi | M. Abbasi | Eduardo Bassone
[1] T. Sundt,et al. Risk of Rupture or Dissection in Descending Thoracic Aortic Aneurysm , 2015, Circulation.
[2] E. Isselbacher,et al. Marfan syndrome is associated with recurrent dissection of the dissected aorta. , 2015, The Annals of thoracic surgery.
[3] J. Coselli,et al. Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations , 2015, Circulation. Cardiovascular genetics.
[4] J. Bavaria,et al. Long-term results of aggressive hemiarch replacement in 534 patients with type A aortic dissection. , 2014, The Journal of thoracic and cardiovascular surgery.
[5] R. Hinton,et al. Twins With Progressive Thoracic Aortic Aneurysm, Recurrent Dissection and ACTA2 Mutation , 2014, Pediatrics.
[6] G. Jondeau,et al. Early-Onset Osteoarthritis, Charcot-Marie-Tooth Like Neuropathy, Autoimmune Features, Multiple Arterial Aneurysms and Dissections: An Unrecognized and Life Threatening Condition , 2014, PloS one.
[7] J. Bavaria,et al. Type A Aortic Dissection in Marfan Syndrome: Extent of Initial Surgery Determines Long-Term Outcome , 2014, Circulation.
[8] V. Aboyans,et al. [2014 ESC Guidelines on the diagnosis and treatment of aortic diseases]. , 2014, Kardiologia polska.
[9] M. Czerny,et al. Acute Aortic Dissection Determines the Fate of Initially Untreated Aortic Segments in Marfan Syndrome , 2013, Circulation.
[10] N. Louis,et al. Fate of the distal aorta after surgical repair of acute DeBakey type I aortic dissection: a review. , 2011, Archives of cardiovascular diseases.
[11] G. Jondeau,et al. Dissection in Marfan syndrome: the importance of the descending aorta. , 2011, European heart journal.
[12] G. Vriend,et al. Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis , 2011, Nature Genetics.
[13] Laurence Faivre,et al. The revised Ghent nosology for the Marfan syndrome , 2010, Journal of Medical Genetics.
[14] David M. Williams,et al. 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, Ame , 2010, Journal of the American College of Cardiology.
[15] J. Coselli,et al. Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations , 2009, Journal of Medical Genetics.
[16] N. Kouchoukos,et al. Aortic enlargement and late reoperation after repair of acute type A aortic dissection. , 2007, The Annals of thoracic surgery.
[17] Rossella Fattori,et al. Partial thrombosis of the false lumen in patients with acute type B aortic dissection. , 2007, The New England journal of medicine.
[18] C. Etz,et al. The fate of the distal aorta after repair of acute type A aortic dissection. , 2007, The Journal of thoracic and cardiovascular surgery.
[19] Robert K. Yu,et al. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections (vol 39, pg 1488, 2007) , 2008 .
[20] P. Byers,et al. Aneurysm syndromes caused by mutations in the TGF-beta receptor. , 2006, The New England journal of medicine.
[21] George H. Thomas,et al. Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor , 2006 .
[22] Wolfram Kress,et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 , 2005, Nature Genetics.
[23] 水口 剛. Heterozygous TGFBR2 mutations in Marfan syndrome , 2005 .
[24] Yusuke Nakamura,et al. Heterozygous TGFBR2 mutations in Marfan syndrome , 2004, Nature Genetics.
[25] A Evangelista,et al. The International Registry of Acute Aortic Dissection (IRAD): new insights into an old disease. , 2000, JAMA.
[26] J. Coselli,et al. Marfan syndrome. Long-term survival and complications after aortic aneurysm repair. , 1995, Circulation.
[27] B. Sonesson,et al. Abnormal mechanical properties of the aorta in Marfan's syndrome. , 1994, European journal of vascular surgery.
[28] V. Kanjuh,et al. Marfan syndrome with aortic dissection and triple-barrel aorta. , 1992, The American journal of cardiovascular pathology.
[29] Ada Hamosh,et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene , 1991, Nature.