{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,7,18]],"date-time":"2024-07-18T21:12:03Z","timestamp":1721337123819},"reference-count":21,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2017,8,1]],"date-time":"2017-08-01T00:00:00Z","timestamp":1501545600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","cardiology.theclinics.com","theclinics.com","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Cardiology Clinics"],"published-print":{"date-parts":[[2017,8]]},"DOI":"10.1016\/j.ccl.2017.03.003","type":"journal-article","created":{"date-parts":[[2017,7,3]],"date-time":"2017-07-03T21:31:10Z","timestamp":1499117470000},"page":"317-320","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"title":["Genetic Disorders of the Thoracic Aorta and Indications for Surgery"],"prefix":"10.1016","volume":"35","author":[{"given":"Jack C.J.","family":"Sun","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"4","key":"10.1016\/j.ccl.2017.03.003_bib1","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1001\/archsurg.134.4.361","article-title":"Familial patterns of thoracic aortic aneurysms","volume":"134","author":"Coady","year":"1999","journal-title":"Arch Surg"},{"issue":"4","key":"10.1016\/j.ccl.2017.03.003_bib2","doi-asserted-by":"crossref","first-page":"1400","DOI":"10.1016\/j.athoracsur.2006.04.098","article-title":"Familial thoracic aortic aneurysms and dissections-incidence, modes of inheritance, and phenotypic patterns","volume":"82","author":"Albornoz","year":"2006","journal-title":"Ann Thorac Surg"},{"issue":"6333","key":"10.1016\/j.ccl.2017.03.003_bib3","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1038\/352337a0","article-title":"Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene","volume":"352","author":"Dietz","year":"1991","journal-title":"Nature"},{"issue":"3","key":"10.1016\/j.ccl.2017.03.003_bib4","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1038\/ng1116","article-title":"Dysregulation of TGF-B activation tonributes to pathogenesis in Marfan syndrome","volume":"33","author":"Neptune","year":"2003","journal-title":"Nat Genet"},{"key":"10.1016\/j.ccl.2017.03.003_bib5","doi-asserted-by":"crossref","first-page":"670","DOI":"10.1016\/j.amjmed.2013.01.029","article-title":"Aortopathies: etiologies, genetics, differential diagnosis, prognosis and management","volume":"126","author":"Paterick","year":"2013","journal-title":"Am J Med"},{"issue":"7","key":"10.1016\/j.ccl.2017.03.003_bib6","doi-asserted-by":"crossref","first-page":"476","DOI":"10.1136\/jmg.2009.072785","article-title":"The revised ghent nosology for the Marfan syndrome","volume":"47","author":"Loeys","year":"2010","journal-title":"J\u00a0Med Genet"},{"issue":"3","key":"10.1016\/j.ccl.2017.03.003_bib7","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1038\/ng1194-264","article-title":"A\u00a0second locus for Marfan syndrome maps to chromosome 3p24.2-p25","volume":"8","author":"Collod","year":"1994","journal-title":"Nat Genet"},{"issue":"8","key":"10.1016\/j.ccl.2017.03.003_bib8","doi-asserted-by":"crossref","first-page":"788","DOI":"10.1056\/NEJMoa055695","article-title":"Aneurysm syndromes caused by mutations in the TGF-B receptor","volume":"355","author":"Loeys","year":"2006","journal-title":"N\u00a0Engl J Med"},{"key":"10.1016\/j.ccl.2017.03.003_bib9","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1016\/j.csm.2015.03.001","article-title":"Diseases of the aorta in elite athletes","volume":"34","author":"Iskandar","year":"2015","journal-title":"Clin Sports Med"},{"issue":"2","key":"10.1016\/j.ccl.2017.03.003_bib10","doi-asserted-by":"crossref","first-page":"73","DOI":"10.3400\/avd.ra.16-00018","article-title":"Aortic aneurysm: etiopathogenesis and clinicopathologic correlations","volume":"9","author":"Ikeda","year":"2016","journal-title":"Ann Vasc Dis"},{"issue":"10","key":"10.1016\/j.ccl.2017.03.003_bib11","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1056\/NEJM200003093421001","article-title":"Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type","volume":"342","author":"Pepin","year":"2000","journal-title":"N\u00a0Engl J Med"},{"issue":"6","key":"10.1016\/j.ccl.2017.03.003_bib12","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1097\/HCO.0000000000000114","article-title":"Familial thoracic aortic aneurysms","volume":"29","author":"Jondeau","year":"2014","journal-title":"Curr Opin Cardiol"},{"issue":"6","key":"10.1016\/j.ccl.2017.03.003_bib13","doi-asserted-by":"crossref","first-page":"1171","DOI":"10.1007\/s10897-016-0002-6","article-title":"Bicuspid aortic valve: a review with recommendations for genetic counseling","volume":"25","author":"Freeze","year":"2016","journal-title":"J\u00a0Genet Couns"},{"key":"10.1016\/j.ccl.2017.03.003_bib14","doi-asserted-by":"crossref","first-page":"735829","DOI":"10.1155\/2012\/735829","article-title":"Pathophysiological implications of different bicuspid aortic valve configurations","volume":"2012","author":"Kari","year":"2012","journal-title":"Cardiol Res Pract"},{"key":"10.1016\/j.ccl.2017.03.003_bib15","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/j.jacc.2004.03.050","article-title":"Bicuspid aortic valve is heritable","volume":"44","author":"Cripe","year":"2004","journal-title":"J\u00a0Am Coll Cardiol"},{"key":"10.1016\/j.ccl.2017.03.003_bib16","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1097\/HCO.0000000000000328","article-title":"Genetics of bicuspid aortic valve aortopathy","volume":"31","author":"Andreassi","year":"2016","journal-title":"Curr Opin Cardiol"},{"key":"10.1016\/j.ccl.2017.03.003_bib17","doi-asserted-by":"crossref","first-page":"1104","DOI":"10.1001\/jama.2011.1286","article-title":"Incidence of aortic complications in patients with bicuspid aortic valves","volume":"306","author":"Michelena","year":"2011","journal-title":"JAMA"},{"key":"10.1016\/j.ccl.2017.03.003_bib18","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1016\/j.jtcvs.2008.01.022","article-title":"The aortopathy of bicuspid aortic valve disease has distinctive patterns and usually involves the transverse aortic arch","volume":"135","author":"Fazel","year":"2008","journal-title":"J\u00a0Thorac Cardiovasc Surg"},{"key":"10.1016\/j.ccl.2017.03.003_bib19","first-page":"2873","article-title":"2014 ESC Guidelines on the diagnosis and greatment of aortic diseases","volume":"35","author":"Erbel","year":"2014","journal-title":"Eur Heart J"},{"issue":"23","key":"10.1016\/j.ccl.2017.03.003_bib20","doi-asserted-by":"crossref","first-page":"e521","DOI":"10.1161\/CIR.0000000000000031","article-title":"2014 AHA\/ACC Guidelines for the management of patients with valvular heart disease: a report of the American College of Cardiology\/American Heart Association task force on practice guidelines","volume":"129","author":"Nishimura","year":"2014","journal-title":"Circulation"},{"key":"10.1016\/j.ccl.2017.03.003_bib21","doi-asserted-by":"crossref","first-page":"e266","DOI":"10.1161\/CIR.0b013e3181d4739e","article-title":"2010 ACCF\/AHA\/AATS\/ACR\/ASA\/SCA\/SCAI\/SIR\/STS\/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease","volume":"121","author":"Hirtazka","year":"2010","journal-title":"Circulation"}],"container-title":["Cardiology Clinics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S073386511730022X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S073386511730022X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,8,30]],"date-time":"2018-08-30T12:55:05Z","timestamp":1535633705000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S073386511730022X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,8]]},"references-count":21,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2017,8]]}},"alternative-id":["S073386511730022X"],"URL":"https:\/\/doi.org\/10.1016\/j.ccl.2017.03.003","relation":{},"ISSN":["0733-8651"],"issn-type":[{"value":"0733-8651","type":"print"}],"subject":[],"published":{"date-parts":[[2017,8]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic Disorders of the Thoracic Aorta and Indications for Surgery","name":"articletitle","label":"Article Title"},{"value":"Cardiology Clinics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ccl.2017.03.003","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}