Disease: Marfan Syndrome type 2
- A novel FBN1 mutation in marfan's syndrome with giant aortic root aneurysm
- A Novel Variant in the FBN1 Gene Causing Marfan Syndrome: A Case Report
- A successful case of deceased-donor liver transplantation from a donor with Marfan syndrome: a case report
- Abnormal Cardiac Magnetic Resonance-Derived Ascending Aortic Area Strain Demonstrates Altered Ventriculo-Vascular Function in Marfan Syndrome
- Activation of the alternative complement pathway modulates inflammation in thoracic aortic aneurysm/dissection
- Ameliorative Effect of Coenzyme Q10 on Phenotypic Transformation in Human Smooth Muscle Cells with <em>FBN1</em> Knockdown
- Angiotensinogen as a Therapeutic Target for Cardiovascular and Metabolic Diseases
- Animal Models, Pathogenesis, and Potential Treatment of Thoracic Aortic Aneurysm
- Aorta pathology and pregnancy-related risks in adult congenital cardiac disease: does the aorta dilate during pregnancy?
- Aortic arch rupture in a patient with Marfan syndrome and previous aortic root repair: A stepwise approach to intraoperative catastrophe
- Association of Ocular Manifestations of Marfan Syndrome With Cardiovascular Complications
- Axillary vs Femoral Arterial Cannulation inĀ Acute Type A Dissection: International Multicenter Data
- Biometric and corneal characteristics in marfan syndrome with ectopia lentis
- Cardiovascular and Obstetric Outcomes Among Delivering Patients with Marfan or Loeys-Dietz Syndrome: A Retrospective Analysis by Hospital Delivery Setting
- Cardiovascular and obstetrical outcomes among delivering patients with Marfan or Loeys-Dietz syndrome: a retrospective analysis by hospital delivery setting
- Chronicle of a death foretold. It is time for echocardiographic screening in young athletes
- CLO24-084: Myeloid Sarcoma in a Patient With Marfan Syndrome
- Coexistence of type 2 diabetes mellitus, arginine vasopressin deficiency, and Marfan syndrome: A case report
- Combined Free-running 4D anatomical and flow MRI with native contrast using Synchronization of Neighboring Acquisitions by Physiological Signals (SyNAPS)
- Combined free-running four-dimensional anatomical and flow magnetic resonance imaging with native contrast using Synchronization of Neighboring Acquisitions by Physiological Signals
- Complicated and Uncomplicated Isolated Abdominal Aortic Dissections Demonstrate Different Patient Characteristics and Outcomes
- Corneal biomechanics and their association with severity of lens dislocation in Marfan syndrome
- 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
- Dural ectasia with cauda equina syndrome, a rare case report
- Early and mid-term outcomes of open thoracoabdominal aortic aneurysm repair after thoracic endovascular aortic repair
- Early-onset Marfan syndrome with aortic dilatation and giant pulmonary artery aneurysm: A case report
- Echogenomics: Echocardiography in Heritable Aortopathies
- EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder
- Endovascular aortic repair in patients with Marfan and Loeys-Dietz syndrome is safe and durable when employed by a multi-disciplinary aortic team
- Endovascular treatment for Stanford type B aortic dissection in Marfan syndrome patients: a series of 23 cases
- Enhanced Optic Nerve Expansion and Altered Ultrastructure of Elastic Fibers Induced by Lysyl Oxidase Inhibition in a Mouse Model of Marfan Syndrome
- Epidermoid Cyst of the Maxillary Sinus: A Case Report and Literature Review
- Extracardiac Manifestations Fail to Predict the Severity of Cardiac Phenotype in Children and Young Adults with Marfan Syndrome
- FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations
- Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations
- Frequency of Cardiac Valvulopathies in Patients With Marfan Syndrome: A Systematic Review and Meta-Analysis
- Genetic mutation and aqueous humor metabolites alterations in a family with Marfan syndrome
- Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia
- Graded Mobilization With Pacing Technique for Functional Mobility in a Preoperative Marfan Syndrome Case of Aortic Root Dilation: A Case Report
- Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study
- Identification of two novel large deletions in FBN1 gene by next-generation sequencing and multiplex ligation-dependent probe amplification
- In vivo phenotypic vascular dysfunction extends beyond the aorta in a mouse model for fibrillin-1 (Fbn1) mutation
- Increased Rate of Complications Following Total Knee Arthroplasty in Patients Who Have Marfan Syndrome
- Influencing factors of effective lens position in patients with Marfan syndrome and ectopia lentis
- Insights on obstetric outcomes in pregnant individuals with Marfan Syndrome: evidence from the National Inpatient Sample
- Integrated DNA methylation analysis reveals a potential role for PTPRN2 in Marfan syndrome scoliosis
- Interprofessional collaboration in the cardiovascular management of Marfan syndrome: A qualitative study based on interviews with professionals
- Long-term results of anterior chamber iris claw intraocular lens implantation in children with ectopia lentis in Marfan syndrome
- Longitudinal changes of refractive error in preschool children with congenital ectopia lentis
- Marfan syndrome
- Marfan syndrome in a Ghanaian male: The diagnostic challenges
- Marfanoid to Mortality: A Case Report on Sudden Cardiac Death Due to Aortic Dissection in a Young Male With Marfanoid Habitus
- miRNA Regulation of Cell Phenotype and Parietal Remodeling in Atherosclerotic and Non-Atherosclerotic Aortic Aneurysms: Differences and Similarities
- Mitral valve surgery in patients with Marfan syndrome
- Natriuretic peptides in the diagnosis and monitoring of heart failure
- Navigating toward gene therapy in Marfan syndrome: A hope for halting aortic aneurysm
- Neurotrophic Keratopathy in Marfan Syndrome Patient After Micropulse Transscleral Cyclophotocoagulation: A Call for Risk Stratification
- New treatment paradigm for patients with Marfan or Loyes-Dietz syndrome
- Novel variant of FBN2 in a patient with congenital contractual arachnodactyly
- Outcomes of complex abdominal wall reconstruction in patients with connective tissue disorders: a single center experience
- Overcoming challenges associated with identifying FBN1 deep intronic variants through whole-genome sequencing
- Paradoxical Changes: EMMPRIN Tissue and Plasma Levels in Marfan Syndrome-Related Thoracic Aortic Aneurysms
- Pathogenic variants affecting the TB5 domain of the fibrillin-1 protein: not only in geleophysic/acromicric dysplasias but also in Marfan syndrome
- Pediatric Microspherophakia Treatment With Scleral Fixated IOL Using a Z-suture Technique
- Pelvic Floor Dysfunction Among Persons With Marfan and Loeys-Dietz Syndrome
- Physical fitness in children with Marfan and Loeys-Dietz syndrome: associations between cardiovascular parameters, systemic manifestations, fatigue, and pain
- Practice Patterns and Barriers to Vascular Genetic Testing among Vascular Surgeons
- Predicting Marfan Syndrome in Children With Congenital Ectopia Lentis: Development and Validation of a Nomogram
- Progressive worsening of aortic regurgitation due to detachment of the aortic valve commissure with multimodality imaging to elucidate pathogenesis: a case report
- Quality of life in young patients with acute type a aortic dissection in China: comparison with Marfan syndrome and non-Marfan syndrome
- Quantitative measurement of dural ectasia: associations with clinical and genetic characteristics in Marfan syndrome
- Rare complications of infective endocarditis in marfan-like morphotype: diagnosis of multiple mitral valve aneurysms and aortic root abscess using three-dimensional transesophageal echocardiography
- Research Progress on Aortic Root Aneurysms
- Safety and Efficacy of Capsular Tension Ring and Capsular Hook Implantation for Managing Ectopia Lentis in Marfan Syndrome: A Real-World Study
- Severe dural ectasia in a pregnant patient with Marfan syndrome
- Short- and Long-term survival prediction in patients with acute type A aortic dissection undergoing open surgery
- Single-Nucleus Multiomic Analyses Identifies Gene Regulatory Dynamics of Phenotypic Modulation in Human Aneurysmal Aortic Root
- Structural and functional features of the eye in Marfan syndrome. Report 1. Changes in the fibrous tunic of the eye
- Structural and functional features of the eye in Marfan syndrome. Report 2. Changes in the anatomical complex of the lens
- Successful endovascular treatment of aortic arch aneurysm in a pediatric patient
- Successful Management of Multiple Giant Anterior Sacral Meningoceles Through an Anterior Approach in a Patient With Marfan Syndrome: A Case Report and Literature Review
- Successful surgical management of a superior cerebellar artery aneurysm in a patient with Marfan syndrome: illustrative case
- Temporomandibular disorders in individuals with Marfan syndrome: an exploratory analysis
- TGFbeta level in healthy and children with Marfan syndrome-effective reduction under sartan therapy
- The Antioxidant Vitamin B12 Analogue Cobinamide as a Treatment for Marfan Syndrome
- The Antioxidant/Nitric Oxide-Quenching Agent Cobinamide Prevents Aortic Disease in a Mouse Model of Marfan Syndrome
- The extracellular matrix glycoprotein fibrillin-1 in health and disease
- The Fbn1 gene variant governs passive ascending aortic mechanics in the mgdelta(lpn) mouse model of Marfan syndrome when superimposed to perlecan haploinsufficiency
- The Impact of Pregnancy in Patients with Thoracic Aortic Disease: Epidemiology, Risk Assessment, and Management Considerations
- The key role of miRNA in syndromic and sporadic forms of ascending aortic aneurysms as biomarkers and targets of novel therapeutic strategies
- The relationship between mitral valve prolapse and thoracic skeletal abnormalities in clinical practice: a systematic review
- The role of genetic testing in Marfan syndrome
- Three-dimensional co-culturing of stem cell-derived cardiomyocytes and cardiac fibroblasts reveals a role for both cell types in Marfan-related cardiomyopathy
- Type A Aortic Dissection in Heart Transplantation Recipients in the United States
- Understanding the links between snoring, OSA and aortic root pathologies in Marfan syndrome
- Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care
- Unraveling the genetic collagen connection: clinical and therapeutic insights on genetic connective tissue disorders
- Vitreous Veils in a Patient with Marfan Syndrome
- Wnt Signaling Inhibition Prevents Postnatal Inflammation and Disease Progression in Mouse Congenital Myxomatous Valve Disease