• 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 loss-of-function cysteine mutant in fibulin-3 (EFEMP1) forms aberrant extracellular disulfide-linked homodimers and alters extracellular matrix composition
• A novel mutation in collagen transport protein, MIA3 gene, detected in a patient with clinical symptoms of Ehlers-Danlos hypermobile syndrome
• A novel pathogenic variant located just upstream of the C-terminal Ser423-X-Ser425 phosphorylation motif in SMAD3 causing Loeys-Dietz syndrome
• 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
• Activation of the alternative complement pathway modulates inflammation in thoracic aortic aneurysm/dissection
• 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
• 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?
• Axillary vs Femoral Arterial Cannulation in Acute Type A Dissection: International Multicenter Data
• 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
• 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
• Complex and Successful Management of a Symptomatic Isolated Abdominal Aortic Aneurysm in a Pregnant Woman with Marfan Syndrome
• Connective tissue disease type mediates branch patency of grafts in open thoracoabdominal aortic reconstruction
• 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
• Effects of changing the timing of warfarin administration in combination with fluconazole on prolongation of the PT-INR: a case report
• 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 Management of Vascular Complications in Ehlers-Danlos Syndrome Type IV
• 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
• Endovascular Treatment of Aortic Pathologies in Patients With Marfan Syndrome: Single-Center Experience
• Experience of the Postoperative Intensive Care Treatment of Stanford Type A Aortic Dissection
• 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
• 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
• 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
• Genetics and pathophysiology of mitral valve prolapse
• Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia
• Hyperkyphosis is not dependent on bone mass and quality in the mouse model of Marfan syndrome
• Hyperuricaemia Does Not Interfere with Aortopathy in a Murine 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
• Initial Angiotensin Receptor Blocker Response in Young Marfan Patients Decreases After 3 Years of Treatment
• Latent TGFbeta-binding proteins 1 and 3 protect the larval zebrafish outflow tract from aneurysmal dilatation
• Latent TGFβ-binding proteins 1 and 3 protect the larval zebrafish outflow tract from aneurysmal dilatation
• 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
• Marfan and Loeys-Dietz aortic phenotype: A potential tool for diagnosis and management
• 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
• Multicentric experience of antegrade thoracic endovascular aortic repair for the treatment of thoracic aortic diseases
• Myopia in the Diagnosis of Marfan Syndrome: An Important Early Sign of a Systemic Condition
• Natural history of the distal aorta following elective root replacement in patients 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
• Paradoxical Changes: EMMPRIN Tissue and Plasma Levels in Marfan Syndrome-Related Thoracic Aortic Aneurysms
• Pathology and pathophysiology of the aortic root
• Pediatric Heart Network Trial of Losartan vs. Atenolol in Children and Young Adults with Marfan Syndrome: Impact on Prescription Practices
• POGLUT2 and POGLUT3 O-glucosylate multiple EGF repeats in fibrillin-1, -2, and LTBP1 and promote secretion of fibrillin-1
• Posttraumatic aortic regurgitation and root pseudoaneurysm following blunt chest trauma: a case report
• 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
• 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
• Retinal detachment in Loeys-Dietz syndrome
• 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
• Severe Aortic Regurgitation of Early Degenerated Mitroflow Bioprosthesis: From Echocardiographic Diagnosis to Treatment with Valve-in-Valve Transcatheter Aortic Valve Implantation
• 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
• Sports Participation and Physical Activity in Individuals with Heritable Thoracic Aortic Disease and Aortopathy Conditions
• Strategies for Treatment of Multiple Brain Aneurysms Without Intraoperative Adjuncts
• Successful management of Stanford type A aortic dissection with severe scoliosis in the setting of Marfan syndrome: a case report
• Successful repair of an arch aneurysm with acute aortic dissection in a patient with Marfan syndrome using a hybrid surgical approach and the stent-assisted balloon-induced intimal disruption and relamination in aortic dissection repair technique
• The fibrotic niche impairs satellite cell function and muscle regeneration in mouse models of Marfan syndrome
• The impact of age in acute type A aortic dissection: a retrospective study
• The impact of sex and gender on aortic events in patients with Marfan syndrome
• The Many Lives of a Complex Marfan Syndrome Patient: Staged Therapeutic Decisions
• 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
• Treatment With Methotrexate Associated With Lipid Core Nanoparticles Prevents Aortic Dilation in a Murine Model of Marfan Syndrome
• Type A Aortic Dissection in Heart Transplantation Recipients in the United States
• Unique robotic vascular surgery procedures
• Unusual combination of acute aortic dissection, Mayer-Rokitansky-Kuster-Hauser syndrome, and 46,XX gonadal dysgenesis: A case report
• Versican accumulation drives Nos2 induction and aortic disease in Marfan syndrome via Akt activation
• What Should We Pay More Attention to Marfan Syndrome Expecting Ectopia Lentis: Incidence and Risk Factors of Retinal Manifestations