• A case of aortic root replacement for annuloaortic ectasia due to Takayasu's arteritis in active inflammatory phase
• A familial missense ACTA2 variant p.Arg198Cys leading to Moyamoya-like arteriopathy with straight course of the intracranial arteries, aortic aneurysm and lethal aortic dissection
• A novel variant in MYLK causes thoracic aortic dissections: genotypic and phenotypic description
• A Retrospective Observational Study to Assess Prescription Pattern in Patients with Type B Aortic Dissection and Treatment Outcome
• Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm
• An Myh11 single lysine deletion causes aortic dissection by reducing aortic structural integrity and contractility
• An upper gastro-intestinal bleeding reveals an aortoesophageal fistula due to the rupture of a thoracic aortic aneurysm
• Annuloaortic Ectasia and Arteritis: Clinical Features, Treatments of Choice, and Causative Relations
• Annuloaortic ectasia associated with antithrombin III deficiency; report of a case
• Annuloaortic Ectasia Associated with Single Coronary Artery and Ventricular Septal Defect;Report of a Case
• Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
• Aortic dilatation and dissection in Turner syndrome: what we know, what we are unclear about and what we should do in clinical practice?
• Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations
• Aortic Dissection and a Previously Unreported <em>ACTA2</em> Missense Variant Mutation in a Young Patient: A Case Report
• Aortic dissection and postpartum cardiomyopathy in a postpartum young woman: a case report study
• Aortic dissection and stroke in a 37-year-old woman: discovering an emerging heritable connective tissue disorder
• Aortic root replacement with absent left-main coronary artery: how to do it
• Aortic squamous metaplasia in a patient with aortoesophageal fistula secondary to thoracic aortic aneurysm: an autopsy case
• Application of postmortem computed tomography angiography to settle a medical dispute after aortic dissection surgery: a forensic case report
• Bentall Procedure for Annuloaortic Ectasia in a Patient with Systemic Lupus Erythematosus;Report of a Case
• Bentall's Procedure for Annuloaortic Ectasia and Severe Aortic Regurgitation in a Patient With Repaired Tetralogy of Fallot and Aortic Valvular Reconstruction
• Bicuspid aortic valve and its ascending aortopathy
• Bilateral axillary artery aneurysms after Bentall procedure in Marfan syndrome
• C-reactive protein, not cardiac troponin T, improves risk prediction in hypertensives with type A aortic dissection
• Chest pain of 48 hours of evolution in a 41 years-old man
• Clinical and genetic characterization of adult patients presenting with non-syndromic vascular aneurysms and dissections
• Clinical outcomes of aortic repair in young adult patients with ACTA2 mutations
• Connective tissue disorders and cardiovascular complications: the indomitable role of transforming growth factor-beta signaling
• Decompressive hemicraniectomy for treatment of space occupying ischemic stroke after repair of type-A aortic dissection
• Deficiency of MMP17/MT4-MMP proteolytic activity predisposes to aortic aneurysm in mice
• Deficits in Col5a2 Expression Result in Novel Skin and Adipose Abnormalities and Predisposition to Aortic Aneurysms and Dissections
• Descending threshold for ascending aortic aneurysmectomy: Is it time for a "left-shift" in guidelines?
• Direct innominate artery cannulation in surgery for annuloaortic ectasia
• Direct visualization of the aortic cusp from the left ventricle during aortic root reimplantation
• Do Familial Aortic Dissections Tend to Occur at the Same Age?
• Double Chambered Right Ventricle with Annuloaortic Ectasia; Report of a Case
• Dual Coronary Compression: An Exceedingly Rare Complication Secondary to Annuloaortic Ectasia
• ELN gene triplication responsible for familial supravalvular aortic aneurysm
• Endovascular repair of an internal mammary artery aneurysm in a patient with SMAD-3 mutation
• Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity
• Exploring the genetic pathogenicity of aortic dissection from 72 Han Chinese individuals using next-generation sequencing
• Familial acute aortic dissection associated with a novel ACTA2 germline variant
• Familial Annulo-aortic Ectasia without Marfan Syndrome
• Familial Aortic Dissection in a Young Adult Caused by MYH11 Gene Mutation
• Familial non-syndromal thoracic aortic aneurysms and dissections - Incidence and family screening outcomes
• Familial thoracic aortic aneurysms
• Familial Thoracic Aortic Dissection
• Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype
• FBN1 mutations largely contribute to sporadic non-syndromic aortic dissection
• Four new cases of pediatric thoracic aortic aneurysm (TAA) with review of the molecular genetic basis, utilizing the newly published consensus nomenclature
• Genetic basis of hereditary thoracic aortic aneurysms and dissections
• Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)
• Genetics, Pregnancy, and Aortic Degeneration
• Giant ascending aortic aneurysm after aortic valve replacement
• Hybrid treatment of aortic arch disease with ascending aorta to carotid artery revascularization and subsequent endovascular repair
• Identification and surgical repair of familial thoracic aortic aneurysm and dissection caused by TGFBR1 mutation
• Identification of three particular morphological phenotypes in sporadic thoracic aortic aneurysm: phenotype III as sporadic thoracic aortic aneurysm biomarker in aged individuals
• Influence of Age on Clinical Presentation, Therapeutic Options, and Outcome in Chinese Patients with Acute Aortic Dissection
• Iris Flocculi as an ocular marker of ACTA2 mutation in familial thoracic aortic aneurysms and dissections
• Iris Flocculi Investigated for Familial Thoracic Aortic Aneurysms and Dissections
• Isolated aortic dilation without osteoarthritis: a case of SMAD3 mutation
• LINC02015 modulates the cell proliferation and apoptosis of aortic vascular smooth muscle cells by transcriptional regulation and protein interaction network
• Long-term follow-up of the femoral artery after total percutaneous endovascular aortic repair with preclose technique using a vascular closure device
• Marfan syndrome, inherited aortopathies and exercise: What is the right answer?
• Mechanical stretch-induced endoplasmic reticulum stress, apoptosis and inflammation contribute to thoracic aortic aneurysm and dissection
• MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections
• Mitral annular disjunction on cardiac MRI: Prevalence and association with disease severity in Loeys-Dietz syndrome
• Multi-Omics of Familial Thoracic Aortic Aneurysm and Dissection: Calcium Transport Impairment Predisposes Aortas to Dissection
• New mechanistic insights to PLOD1-mediated human vascular disease
• New mutation in the ACTA2 gene (p.Met84Val) in a family with nonsyndromic familial aortic aneurysms
• Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome
• Nonsyndromic familial aortic disease: an underdiagnosed entity
• Novel <em>LOX</em> Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings
• Novel findings: Expression of angiotensin-converting enzyme and angiotensin-converting enzyme 2 in thoracic aortic dissection and aneurysm
• Outcomes of Early-Onset Acute Type A Aortic Dissection　- Influence of Etiologic Factors
• Pathogenic FBN1 variants in familial thoracic aortic aneurysms and dissections
• Proteoglycans and diseases of soft tissues
• Proteomic study of the microdissected aortic media in human thoracic aortic aneurysms
• Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
• Repair of idiopathic ascending aortic aneurysm in a 7-year-old child
• Repair of pectus excavatum and aortic valve-sparing operation: One-stage strategy
• Replacement of the aortic root with a composite valve-graft conduit: risk factor analysis in 246 consecutive patients
• Root aneurysm following aortic valve replacement 20 years after an arterial switch operation
• rs10263935 and rs6045676 identified by genome-wide association study were associated with aortic dissection in a Chinese population
• Simultaneous cusp-sparing aortic root replacement and coarctectomy with total arch replacement from the midline incision
• Successful aortic root replacement and shunt closure in a case with rare coexistence of congenital cardiac malformations: bicuspid aortic valve with annuloaortic ectasia, single coronary artery, and patent foramen ovale
• Successful management of spontaneous aortic dissection type B in the third trimester of pregnancy
• Surgery for detached coronary ostial anastomosis 21 years post-Bentall procedure
• Symptomatic familial primary iris cysts at the pupillary margin in three consecutive generations: A case series
• Systematic Review of Studies That Have Evaluated Screening Tests in Relatives of Patients Affected by Nonsyndromic Thoracic Aortic Disease
• Targeted Panel Sequencing Identifies an Intronic c.5225-3C&gt;G Variant of the <em>FBN1</em> Gene Causing Sporadic Marfan Syndrome with Annuloaortic Ectasia
• The effects of acute and elective cardiac surgery on the anxiety traits of patients with Marfan syndrome
• The many faces of IgG4-related disease: report of a case with inaugural recurrent aortic aneurism ruptures and literature review
• Thoracic Aneurysms and Dissections: Towards a Further and Better Knowledge
• Thoracic Aortic Dissection Associated with Marijuana Use
• Tricuspidization and reimplantation procedure for unicuspid aortic valve with annuloaortic ectasia
• Valve-Sparing Root Replacement in Elderly Patients With Annuloaortic Ectasia
• Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection
• Vascular disease-causing mutation, smooth muscle α-actin R258C, dominantly suppresses functions of α-actin in human patient fibroblasts
• Ventricular-Vascular Coupling in Marfan and Non-Marfan Aortopathies