• <em>Fibrillin-1</em> gene mutations in a Chinese cohort with congenital ectopia lentis: spectrum and genotype-phenotype analysis
• <em>MED12</em>-Related (Neuro)Developmental Disorders: A Question of Causality
• 4D flow MRI of type B dissection with later retrograde progression to type A dissection in Marfan: a case report
• A comparison of bilateral and unilateral cerebral perfusion for total arch replacement surgery for non-marfan, type A aortic dissection
• A Rare Case Of Shprintzen-Goldberg Syndrome
• A systematic review supporting the Society for Vascular Surgery guidelines on the management of heritable aortopathies
• A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
• A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
• Acceptance and commitment therapy meets peer-support. Development of a supportive self-care intervention for patients with rare diseases: a multistage development process
• Acute Aortic Dissection Type A in Younger Patients (&lt; 60 Years Old) - Does Full Arch Replacement Provide Benefits Compared to Limited Approach?
• Acute Aortic Dissection Type A in Younger Patients (< 60 Years Old) - Does Full Arch Replacement Provide Benefits Compared to Limited Approach?
• Acute dissection into a large abdominal aortic aneurysm in a patient with Marfan syndrome
• Acute type A aortic dissection in adolescents and young adults under 30 years of age: demographics, aetiology and postoperative outcomes of 139 cases
• Acute type A aortic dissection in young adults: a field yet to explore
• Age-related difference in acute type B aortic dissection
• Analysis of factors influencing the remodeling of abdominal false lumen after thoracic aortic endovascular repair
• Anterior megalophthalmos in sisters with Witteveen-Kolk syndrome
• Aortic Dissection During Pregnancy and Puerperium: Contemporary Incidence and Outcomes in the United States
• Aortic events in pregnant patients with Marfan syndrome. Lessons from a multicenter study
• Aortic valve reimplantation in patients with connective tissue syndromes: A 15-year follow-up
• Aortic valve-sparing root replacement with Tirone E. David's reimplantation technique: single-centre 25-year experience
• Are acute type A aortic dissections atherosclerotic?
• Can Hemorrhagic Stroke Genetics Help Forensic Diagnosis in Pediatric Age (<5 Years Old)?
• Can preoperative features predict residual false lumen remodelling after tear-oriented limited resection for acute type I dissection?
• Cardiovascular Events After Aortic Root Repair in Patients With Marfan Syndrome
• Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome
• Complex and Successful Management of a Symptomatic Isolated Abdominal Aortic Aneurysm in a Pregnant Woman with Marfan Syndrome
• Complicated and Uncomplicated Isolated Abdominal Aortic Dissections Demonstrate Different Patient Characteristics and Outcomes
• Connective tissue disease type mediates branch patency of grafts in open thoracoabdominal aortic reconstruction
• Delineation of dual molecular diagnosis in patients with skeletal deformity
• Diameter and dissection of the abdominal aorta and the risk of distal aortic reoperation after surgery for type A aortic dissection
• Direct sac puncture embolization for a left subclavian aneurysm with Marfan syndrome: A case report
• Early and long-term outcomes of young adult patients ≤30 years old with acute type A aortic dissection
• Early and long-term outcomes of young adult patients 30 years old with acute type A aortic dissection
• Early outcomes of patients with Marfan syndrome and acute aortic type A dissection
• En Bloc Arch Reconstruction With the Frozen Elephant Trunk Technique for Acute Type a Aortic Dissection
• Endovascular and Hybrid Repair in Patients with Heritable Thoracic Aortic Disease
• Endovascular therapy for Stanford B aortic dissection for patients with Marfan Syndrome: systematic review and meta-analysis
• Endovascular treatment for Stanford type B aortic dissection in Marfan syndrome patients: a series of 23 cases
• Extended Stent Coverage Decreases Distal Aortic Segmental Enlargement After the Endovascular Repair of Acute Complicated Type B Aortic Dissection: A Multi-Center Retrospective Study of 814 Patients
• Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome
• Factors affecting distal false lumen enlargement after thoracic endovascular aortic repair for type B aortic dissection
• Factors Associated with Nontraumatic Spontaneous Subdural Hematomas in Pediatric Patients
• Fate of remaining dissected aorta after descending thoracic or thoracoabdominal aorta replacement for chronic dissection
• Fatigue in patients with syndromic heritable thoracic aortic disease: a systematic review of the literature and a qualitative study of patients' experiences and perceptions
• Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations
• Florida sleeve is a safe and effective technique for valve salvage in acute stanford type A aortic dissection
• FN (Fibronectin)-Integrin alpha5 Signaling Promotes Thoracic Aortic Aneurysm in a Mouse Model of Marfan Syndrome
• FN (Fibronectin)-Integrin α5 Signaling Promotes Thoracic Aortic Aneurysm in a Mouse Model of Marfan Syndrome
• Frequency of Arrhythmias and Postural Orthostatic Tachycardia Syndrome in Patients With Marfan Syndrome: A Nationwide Inpatient Study
• Genome-wide methylation patterns in Marfan syndrome
• Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia
• Heart Transplantation After Acute Aortic Dissection in an Adolescent With Marfan Syndrome
• Heterogenous improvements in endothelial function by sub-blood pressure lowering doses of ARBs result in major anti-aortic root remodeling effects
• Hyperkyphosis is not dependent on bone mass and quality in the mouse model of Marfan syndrome
• Identification of two variants in PAX3 and FBN1 in a Chinese family with Waardenburg and Marfan syndrome via whole exome sequencing
• Impact of Notch3 Activation on Aortic Aneurysm Development in Marfan Syndrome
• In-hospital outcomes and long-term survival of women of childbearing age with aortic dissection
• Inhibition of IL11 Signaling Reduces Aortic Pathology in Murine Marfan Syndrome
• Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome
• Is the intimal thickness a key contributor to thoracic aortopathy?
• Long-term outcomes in heritable thoracic aortic disease
• Magnetic resonance angiography derived predictors of progressive dilatation and surgery of the aortic root in Marfan syndrome
• Matched comparison between external aortic root support and valve-sparing root replacement
• Modified "<em>in situ</em>" arch replacement with an integrative frozen elephant trunk device for acute type A aortic dissection
• Modified "in situ" arch replacement with an integrative frozen elephant trunk device for acute type A aortic dissection
• Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort
• Multicentre experience of antegrade thoracic endovascular aortic repair for the treatment of thoracic aortic diseases
• Naringenin inhibits thoracic aortic aneurysm formation in mice with Marfan syndrome
• Open surgical replacement of the descending thoracic and thoracoabdominal aorta in patients with confirmed Marfan and Loeys-Dietz syndromes: A 20-year single-centre experience
• Outcome of Stanford type B dissection in patients with Marfan syndrome
• Outcomes After Endovascular Aortic Intervention in Patients With Connective Tissue Disease
• Outcomes of endovascular therapy for Stanford type B aortic dissection in patients with Marfan syndrome
• Outcomes of endovascular therapy for Stanford type B aortic dissection in patients with sleep apnea syndrome
• Outcomes of surgical intervention in cases of ectopia lentis
• Passing a Mechanical Aortic Valve With a Short Tip Dilator to Facilitate Aortic Arch Endovascular Branched Repair
• Percutaneous gluteal artery access to embolize false lumen of type B aortic dissection in marfan patient
• Prediction Model for Postoperative Pressure Injury in Patients with Acute Type A Aortic Dissection
• Pregnancy-Related Aortic Complications in Women With Marfan Syndrome
• Prescription pattern and effectiveness of antihypertensive drugs in patients with aortic dissection who underwent surgery
• Prevalence and Complications of Aberrant Subclavian Artery in Patients With Heritable and Nonheritable Arteriopathies
• Rare complication of a type IV paraoesophageal hiatal hernia in a Marfan syndrome patient
• Relationship between phenotypic features in Loeys-Dietz syndrome and the presence of intracranial aneurysms
• Reoperation after Implanting a Triple-Branched Stent Graft: Case Report
• Results of a prospective follow-up study after type A aortic dissection repair: a high rate of distal aneurysmal evolution and reinterventions
• Retinal detachment in Loeys-Dietz syndrome
• Retrograde Stanford Type A Aortic Dissection of Marfan Syndrome Long After Thoracic Endovascular Aortic Repair:Report of a Case
• Safety and Effectiveness of TEVAR in Native Proximal Landing Zone 2 for Chronic Type B Aortic Dissection in Patients With Genetic Aortic Syndrome
• Simple Death Risk Models to Predict In-hospital Outcomes in Acute Aortic Dissection in Emergency Department
• Synchrotron Radiation-based X-ray phase-contrast imaging of the aortic walls in acute aortic dissection
• The fibrotic niche impairs satellite cell function and muscle regeneration in mouse models of Marfan syndrome
• The impact of sex and gender on aortic events in patients with Marfan syndrome
• The relationship between mitral valve prolapse and thoracic skeletal abnormalities in clinical practice: a systematic review
• Thoracic aneurysm and dissection gene variants increase the risk of aortic-related adverse events in early-onset isolated Stanford type B aortic dissection after endovascular aortic repair
• Treatment of the aortic root in acute aortic dissection type A: insights from the German Registry for Acute Aortic Dissection Type A
• Treatment of the Aortic Root in Acute Aortic Dissection Type A: Insights from the German Registry for Acute Aortic Dissection Type A (GERAADA) Registry
• Type A Aortic Dissection in Heart Transplantation Recipients in the United States
• Unique robotic vascular surgery procedures
• Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome
• What Should We Pay More Attention to Marfan Syndrome Expecting Ectopia Lentis: Incidence and Risk Factors of Retinal Manifestations