• A Case of Marfan Syndrome With Congenital Hip Dysplasia and Spine Abnormality
• A case of total arch replacement in a patient with Marfan syndrome using a continuous-flow left ventricular assist device
• A Novel Variant in the FBN1 Gene Causing Marfan Syndrome: A Case Report
• Acute ischemic stroke with a diagnosis of Marfan syndrome: A report of 3 cases in multifaceted settings
• An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome
• Anterior scleral thickness in Marfan syndrome: A quantitative analysis
• Aortic size distribution among normal, hypertension, bicuspid, and Marfan populations
• Aortopathy - A surgical pathology experience
• Are aortic biomechanical properties early markers of dilatation in patients with Marfan syndrome? A systematic review and meta-analysis
• Assessment of extra-coronary peripheral arteriopathy in spontaneous coronary dissection: state of the art in non-invasive imaging techniques and future perspectives
• Atrial septal defect becoming clinically evident after cardiac surgery for annuloaortic ectasia: a case report
• Beaded aneurysm of the descending aorta in a Marfan syndrome patient due to wrapping 35 years ago
• Can Hemorrhagic Stroke Genetics Help Forensic Diagnosis in Pediatric Age (<5 Years Old)?
• Cardiovascular Management of Aortopathy in Children: A Scientific Statement From the American Heart Association
• Causative role of a novel intronic indel variant in FBN1 and maternal germinal mosaicism in Marfan syndrome
• Cerebral Microvascular Density, Permeability of the Blood-Brain Barrier, and Neuroinflammatory Responses Indicate Early Aging Characteristics in a Marfan Syndrome Mouse Model
• Challenges in prompt identification and surgical correction of Marfan Syndrome aortic disease in a middle-income country: a case series study
• Coding and Non-Coding Transcriptomic Landscape of Aortic Complications in Marfan Syndrome
• Coexistence of Marfan syndrome and fibromuscular dysplasia
• Commentator Discussion: Mitral valve surgery in patients with Marfan syndrome
• Comparative Analysis of Long-Term Outcomes in Thoracoabdominal Aortic Aneurysm Repair Between Marfan Syndrome and Non-Marfan Syndrome Patients
• Complement C3a/C3aR inhibition alleviates the formation of aortic aneurysm in Marfan syndrome mice
• Congenital right subclavian artery aneurysm resection in a 30-year-old woman
• Correction: Surgical outcome of scoliosis in patients with Marfan syndrome
• Correlation of posterior segment lesions with anterior segment biometric parameters and FBN1 genotype in patients with Marfan syndrome
• Diagnosis of Marfan Syndrome Following Progressive Myopia and Secondary Lens-Induced Angle Closure Crisis
• Disorders with Ophthalmic and Thoracic Involvement
• Double somatic mosaicism in Marfan syndrome
• Dyspnoea in a young woman
• Ectopia Lentis: Clinical profiles in a large cohort of children from a Tertiary Eye Care network in India
• Elastin turnover in Williams-Beuren and 7q11.23 microduplication syndromes
• Epidermoid Cyst of the Maxillary Sinus: A Case Report and Literature Review
• Evidence of cardiomyopathy associated with Marfan syndrome in children
• Extracardiac Manifestations Fail to Predict the Severity of Cardiac Phenotype in Children and Young Adults with Marfan Syndrome
• Familial Ectopia Lentis: Looking Beyond Marfan's Syndrome
• Generation of an induced pluripotent stem cell line, JHUi005-A, from a Marfan Syndrome patient harboring a pathogenic c.3338-2A>C intronic splicing variant
• Generation of Marfan syndrome-specific induced pluripotent stem cells harboring FBN1 mutations
• Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia
• Genotype-phenotype Correlations of Ocular Posterior Segment Abnormalities in Marfan Syndrome
• Giant left atrium in a patient with Marfan syndrome
• Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study
• Hereditary Aortic Aneurysms and Dissections: Clinical Diagnosis and Genetic Testing
• High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects
• Human Genetics of Ventricular Septal Defect
• Impact of the US Food and Drug Administration warning regarding increased risk of aortic aneurysms or aortic dissections on fluoroquinolone prescribing trends
• Incidence and Outcomes of Brucella Endocarditis in a High-Prevalence Area: A Single-Center Study
• Innovation in pathogenesis and management of aortic aneurysm
• Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome
• Letter regarding "The usefulness of the genetic panel in the classification and refinement of diagnostic accuracy of Mexican patients with Marfan syndrome and other connective tissue disorders"
• Long-Term Postoperative Outcomes following Cionni Ring and In-the-Bag Intraocular Lens Implantation in Eyes with Subluxated Lenses
• Long-term results of anterior chamber iris claw intraocular lens implantation in children with ectopia lentis in Marfan syndrome
• Longitudinal echocardiography in pediatric patients with hypermobile Ehlers-Danlos syndrome
• Management of a pregnant woman with Marfan syndrome and aortic root and aberrant right subclavian artery aneurysm: a case report
• Management of an elderly patient with nonsyndromic <em>TGFBR1</em>-related aortopathy: A case report
• Marfan and Loeys-Dietz aortic phenotype: A potential tool for diagnosis and management
• Marfan Syndrome Associated With Acute Myocardial Infarction in the First Trimester of Pregnancy
• Marfan syndrome presenting as an air leak syndrome!
• Marfan's syndrome is associated with a greater risk of Peyronie's disease: a case-control study of the TriNetX database
• miRNA-Driven Regulation of Endothelial-to-Mesenchymal Transition Differs among Thoracic Aortic Aneurysms
• Mitral Annular Disjunction and Its Progression during Childhood in Marfan Syndrome
• Mitral valve surgery in patients with Marfan syndrome
• Mitral valve transcatheter edge-to-edge repair as a bridge to treat aortic dissecting aneurysm in a case of Marfan syndrome: a case report
• MRI-Derived Dural Sac and Lumbar Vertebrae 3D Volumetry Has Potential for Detection of Marfan Syndrome
• 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
• Multidisciplinary follow-up in a patient with Morgagni hernia leads to diagnosis of Marfan syndrome
• National registry insights on genetic aortopathies and thoracic endovascular aortic interventions
• Neurological abnormalities in individuals with Marfan syndrome: results from a genetically confirmed Italian cohort
• Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic Diseases
• Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature
• Outcomes of endovascular therapy for Stanford type B aortic dissection in patients with sleep apnea syndrome
• Percutaneous gluteal artery access to embolize false lumen of type B aortic dissection in marfan patient
• Pilot study exploring artificial intelligence for facial-image-based diagnosis of Marfan syndrome
• Posttraumatic aortic regurgitation and root pseudoaneurysm following blunt chest trauma: a case report
• Proteomics analysis on aortic smooth muscle cells reveals new potential targets for the treatment of Marfan syndrome-associated thoracic aortic aneurysm
• Pulmonary artery aneurysm: computed tomography (CT) imaging findings and diagnosis
• Rare but There: Ceftriaxone-Induced Neutropenia in a Patient With a Brain Abscess
• Repair of popliteal aneurysm and spontaneous arteriovenous fistula in a patient with Marfan syndrome
• Response to the Letter regarding "The usefulness of the genetic panel in the classification and refinement of diagnostic accuracy of Mexican patients with Marfan syndrome and other connective tissue disorders"
• Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India
• Retrograde Stanford Type A Aortic Dissection of Marfan Syndrome Long After Thoracic Endovascular Aortic Repair:Report of a Case
• Reviewing hereditary connective tissue disorders: Proposals of harmonic medicolegal assessments
• Right ventricular function in marfan patients remains stable despite multiple cardiac interventions
• Risk Factors for Retinal Detachment in Marfan Syndrome After Pediatric Lens Removal
• Self-care behaviors and their individual-level determinants in Italian adults with Marfan syndrome: A single-center cross-sectional study
• Serous-Exudative Detachment and Progressive Macular Degeneration in a Patient With Kabuki and Marfan Syndrome
• Single-stage total aortic replacement in a young patient with chronic type A aortic dissection, Marfan and mega-aorta syndromes
• Skin mast cells in Marfan syndrome: specific emphasis on connective tissue remodeling
• Spontaneous Intracranial Hypotension Associated with Marfan Syndrome: A Case Report
• Sunrise in the eye: Bilateral superonasal lens subluxation in Marfan syndrome
• Targeted next-generation sequencing reveals the genetic mechanism of Chinese Marfan syndrome cohort with ocular manifestation
• Tissue material properties, whole-bone morphology and mechanical behavior in the Fbn1 (C1041G/+) mouse model of Marfan syndrome
• Transscleral fixation of intraocular lens in the treatment of lens subluxation in children
• Treatment and Outcomes of 844 Cases of Pneumothorax in Heritable Connective Tissue Disorders
• Uncovering an Unusual FBN1 Gene Mutation Responsible for Marfan Syndrome: A Case Study
• Updated 2022 ACC/AHA Guideline Improves Concordance Between TTE and CT in Monitoring Marfan Snydrome and Related Disorders, but Relevant Measurement Differences Remain Frequent
• Valvulopathies and Genetics: Where are We?
• Visual Outcomes in Ectopia Lentis in Marfan Syndrome: A Study of Four Surgical Techniques in Children and Adults
• Vitreous Veils in a Patient with Marfan Syndrome
• Zonular fibre Insertion-to-Limbus Distance (ZLD): normative data to assess lens position and diagnose ectopia lentis