• A comparison of bilateral and unilateral cerebral perfusion for total arch replacement surgery for non-marfan, type A aortic dissection
• A comprehensive analysis of FBN2 in bladder cancer: A risk factor and the tumour microenvironment influencer
• A systematic review supporting the Society for Vascular Surgery guidelines on the management of heritable aortopathies
• Acceptance and commitment therapy meets peer-support. Development of a supportive self-care intervention for patients with rare diseases: a multistage development process
• Activation of the alternative complement pathway modulates inflammation in thoracic aortic aneurysm/dissection
• Acute inferior wall myocardial infarction induced by aortic dissection in a young adult with Marfan syndrome: A case report
• Acute type A aortic dissection in adolescents and young adults under 30 years of age: demographics, aetiology and postoperative outcomes of 139 cases
• Age-related difference in acute type B aortic dissection
• Aortic dissection during pregnancy and puerperium: A Japanese nationwide survey
• Aortic Dissection During Pregnancy and Puerperium: Contemporary Incidence and Outcomes in the United States
• Aortic valve reimplantation in patients with connective tissue syndromes: A 15-year follow-up
• Application of branch-first technique in total thoracic aorta replacement: short and medium term effect of 11 cases
• Are acute type A aortic dissections atherosclerotic?
• Bentall Procedure to Repair Acute Type a Aortic Dissection in Pregnant Marfan Syndrome Woman With Preservation of Pregnancy
• Blood pressure-independent inhibition of Marfan aortic root widening by the angiotensin II receptor blocker valsartan
• Case Report: Effects of Sars-CoV-2 on Marfan syndrome with resulting acute aortic dissection
• Cataract surgery outcomes in pediatric patients with systemic comorbidities
• Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome
• Characterization of syndromic, nonsyndromic familial, and sporadic type B aortic dissection
• Clinical Features and Outcomes of Pregnancy-Related Acute Aortic Dissection
• Complicated and Uncomplicated Isolated Abdominal Aortic Dissections Demonstrate Different Patient Characteristics and Outcomes
• Diameter and dissection of the abdominal aorta and the risk of distal aortic reoperation after surgery for type A aortic dissection
• Differential Diagnosis between Marfan Syndrome and Loeys-Dietz Syndrome Type 4: A Novel Chromosomal Deletion Covering TGFB2
• Early outcomes of patients with Marfan syndrome and acute aortic type A dissection
• Effects of Age, Sex, and Extracellular Matrix Integrity on Aortic Dilatation and Rupture in a Mouse Model of Marfan Syndrome
• Ehlers-Danlos Syndrome: Immunologic contrasts and connective tissue comparisons
• 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 of a Ruptured Pseudoaneurysm of the Intercostal Patch after Descending Aortic Aneurysm Repair
• Endovascular Treatment of Aortic Pathologies in Patients With Marfan Syndrome: Single-Center Experience
• Evaluating the sagittal spinal and pelvic parameters in Marfan syndrome patients affected by scoliosis
• Exploring the potential relationship between collagen cross-linking and impaired myocardial relaxation in Marfan syndrome: An observational study using serum biomarkers
• 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
• 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
• Fenestration of the intima to facilitate successful endovascular repair of a dissecting abdominal aneurysm
• Fibrillin-1 deficiency in the outer perichondrium causes longitudinal bone overgrowth in mice with Marfan syndrome
• Florida sleeve is a safe and effective technique for valve salvage in acute stanford type A aortic dissection
• Frequency of Arrhythmias and Postural Orthostatic Tachycardia Syndrome in Patients With Marfan Syndrome: A Nationwide Inpatient Study
• Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia
• Heterogenous improvements in endothelial function by sub-blood pressure lowering doses of ARBs result in major anti-aortic root remodeling effects
• High fat diet has a protective sex-dependent effect on aortic aneurysm severity in a Marfan syndrome mouse model
• High-Fat Diet Has a Protective Sex-Dependent Effect on Aortic Aneurysm Severity in a Marfan Syndrome Mouse Model
• 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
• In-hospital outcomes and long-term survival of women of childbearing age with aortic dissection
• Interventional Dilemma in a Young Woman With Spontaneous Coronary Artery Dissection Who Presented With High-Risk Non-ST-Elevation Myocardial Infarction (NSTEMI) Progressing to ST-Elevation Myocardial Infarction (STEMI)
• Long-term outcomes in heritable thoracic aortic disease
• Marfan Treatment Trialists' Collaboration in perspective: Sartans and beta-blockers in patients with Marfan syndrome
• Matched comparison between external aortic root support and valve-sparing root replacement
• MitraClip used for severe mitral regurgitation after surgery for type A aortic dissection combined with Marfan syndrome
• 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
• Multicentre experience of antegrade thoracic endovascular aortic repair for the treatment of thoracic aortic diseases
• Multicentric experience of antegrade thoracic endovascular aortic repair for the treatment of thoracic aortic diseases
• Multiple Arterial Dissections and Connective Tissue Abnormalities
• National trends in thoracic aortic aneurysms and dissections in patients with Marfans and Ehlers Danlos syndrome
• Natural history of the distal aorta following elective root replacement in patients with Marfan syndrome
• New pharmacological agents and novel cardiovascular pharmacotherapy strategies in 2022
• Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic Diseases
• Outcome of Stanford type B dissection in patients with Marfan syndrome
• Outcomes After Endovascular Aortic Intervention in Patients With Connective Tissue Disease
• Outcomes of aortic root replacement in patients with Marfan syndrome: the role of valve-sparing and valve-replacing approaches
• 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
• Predicting Intensive Care Unit Length of Stay After Acute Type A Aortic Dissection Surgery Using Machine Learning
• 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
• Protection and delay of aortic complications in the Marfan syndrome: a new indication for angiotensin receptor blockers on top of beta blockers
• Protection and delay of aortic complications in the Marfan syndrome: a new indication for angiotensin receptor blockers on top of β blockers
• Rare complication of a type IV paraoesophageal hiatal hernia in a Marfan syndrome patient
• Redo surgery for a type A aortic dissection in a pregnant woman with Marfan syndrome: a complex clinical case
• Relationship between phenotypic features in Loeys-Dietz syndrome and the presence of intracranial aneurysms
• Results of a prospective follow-up study after type A aortic dissection repair: a high rate of distal aneurysmal evolution and reinterventions
• Risk of Type B Dissection in Marfan Syndrome: The Cornell Aortic Aneurysm Registry
• Risk profile and operative outcomes in patients with and without Marfan syndrome undergoing thoracoabdominal aortic aneurysm repair
• Simple Death Risk Models to Predict In-hospital Outcomes in Acute Aortic Dissection in Emergency Department
• Smooth Muscle Cell Relaxation Worsens Aortic Dilatation and Clinical Presentation in a BAPN/Angiotensin II-Induced Aortic Dissection Model in Rats
• Staged hybrid repair of type II thoracoabdominal aneurysms
• Successful Mitral Valve Replacement in an Infant with Neonatal Marfan Syndrome due to a Novel Missense Mutation of the FBN1 Gene
• Systematic review and meta-analysis of aortic valve-sparing surgery versus replacement surgery in ascending aortic aneurysms and dissection in patients with Marfan syndrome and other genetic connective tissue disorders
• Ten-Year Clinical Characteristics and Early Outcomes of Type B Aortic Dissection Patients With Thoracic Endovascular Aortic Repair
• The impact of sex and gender on aortic events in patients with Marfan syndrome
• The Late Effects of Pregnancy on Aortic Dimensions in Patients with Marfan Syndrome
• The Utility of Paraspinal Acoustic Windows for the Evaluation of Acute Dissection of Descending Thoracic Aorta in the Emergency Setting
• Therapeutic CCR2 Blockade Prevents Inflammation and Alleviates Myxomatous Valve Disease in Marfan Syndrome
• 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 aneurysms having modelled pre-dissection maximum diameter below 45 mm: should we implement current guidelines to improve the survival benefit of prophylactic surgery?
• Unique robotic vascular surgery procedures
• Unusual presentation of Loeys-Dietz syndrome: A case report of clinical findings and treatment challenges
• Versican accumulation drives Nos2 induction and aortic disease in Marfan syndrome via Akt activation
• Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome
• Weak Ligaments and Sloping Joints: A New Hypothesis for Development of Congenital Atlantoaxial Dislocation and Basilar Invagination
• What Should We Pay More Attention to Marfan Syndrome Expecting Ectopia Lentis: Incidence and Risk Factors of Retinal Manifestations