Disease: Aortic aneurysm- familial thoracic 4
- A highly penetrant ACTA2 mutation of thoracic aortic disease
- Acute type A aortic dissection in adolescents and young adults under 30 years of age: demographics, aetiology and postoperative outcomes of 139 cases
- Annuloaortic Ectasia and Arteritis: Clinical Features, Treatments of Choice, and Causative Relations
- Annuloaortic ectasia in a four-month-old male Newfoundland dog: long-term follow-up and immunofluorescent study
- Aortic dissection in a young male with persistent ductus arteriosus and a novel variant in MYLK
- Ascending Aortic Aneurysm in an Asymptomatic Young Woman Without Risk Factors
- Association Between Genetic Diagnosis and Clinical Outcomes in Patients With Heritable Thoracic Aortic Disease
- Cardiovascular involvement and prognosis in Loeys-Dietz syndrome
- Challenges of Managing Non-rheumatic Aortic Valve Disorder in a Genetically Susceptible Woman
- Clinical and genetic characterization of adult patients presenting with non-syndromic vascular aneurysms and dissections
- Clinical Interpretation of Genetic Variants in the Evaluation and Management of Thoracic Aortic Aneurysm and Dissection
- Clinical outcomes of aortic repair in young adult patients with ACTA2 mutations
- Contributions of Germline and Somatic Mosaic Genetics to Thoracic Aortic Aneurysms in Nonsyndromic Individuals
- Derivation and Validation of Spontaneous Coronary Artery Dissection Prediction Score in Patients With Myocardial Infarction
- Do Familial Aortic Dissections Tend to Occur at the Same Age?
- Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity
- Familial Associations of Prevalence and Cause-Specific Mortality for Thoracic Aortic Disease and Bicuspid Aortic Valve in a Large-Population Database
- Family history as the strongest predictor of aortic and peripheral aneurysms in patients with intracranial aneurysms
- Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture
- Genetic aortopathies: a case-based approach to multidisciplinary program development
- 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
- Glycaemic Status and Risk of Abdominal Aortic Aneurysm: A Nationwide Cohort Study of Four Million Adults using Korean National Health Screening Data
- HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN
- Incidence and risk factors for interval aortic events during staged fenestrated-branched endovascular aortic repair
- Metabolic syndrome and the risk of abdominal aortic aneurysm: A nationwide cohort study
- New mutation in the ACTA2 gene (p.Met84Val) in a family with nonsyndromic familial aortic aneurysms
- Nonsize Criteria for Surgical Intervention on the Ascending Thoracic Aorta
- Novel <em>LOX</em> Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings
- Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic Diseases
- Outcomes of Early-Onset Acute Type A Aortic Dissection　- Influence of Etiologic Factors
- Patterns of genetic mutations explored by systematic screening of patients with aortopathy and their family members
- Siblings with profound connective tissue disease: First report of biallelic TGFBR1-related Loeys-Dietz syndrome
- Sinus of Valsalva Aneurysm in Females
- Survival, Short And Long-Term Outcomes Of Open And Endovascular Surgical Repair Of Unruptured Infrarenal Abdominal Aortic Aneurysms
- Systematic review of cardiovascular neurocristopathy-contemporary insights and future perspectives
- Targeted Proteomic Analysis of Patients with Ascending Thoracic Aortic Aneurysm
- The effects of acute and elective cardiac surgery on the anxiety traits of patients with Marfan syndrome
- The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases
- Thoracic Aneurysms and Dissections: Towards a Further and Better Knowledge
- Thoracic Aortic Aneurysm and Dissection: Review and Recommendations for Evaluation
- Valve-Sparing Root Replacement in Elderly Patients With Annuloaortic Ectasia
- Variable clinical expression of a Belgian <em>TGFB3</em> founder variant suggests the presence of a genetic modifier
- Ventricular-Vascular Coupling in Marfan and Non-Marfan Aortopathies
- Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysm