All Stories

  1. Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review
  2. Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome
  3. Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice
  4. Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome
  5. Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome
  6. Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Huma...
  7. Real-world healthcare utilization in adult congenital heart disease: a systematic review of trends and ratios
  8. Disproportion and dysmorphism in an adult Belgian population with Turner syndrome: risk factors for chronic diseases?
  9. Staffing, activities, and infrastructure in 96 specialised adult congenital heart disease clinics in Europe
  10. Vascular Ehlers-Danlos Syndrome Management
  11. SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections
  12. Body mass index in adults with congenital heart disease
  13. SMAD3 pathogenic variants: risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium
  14. OUP accepted manuscript
  15. Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association
  16. Cardiovascular imaging in Turner syndrome: state-of-the-art practice across the lifespan
  17. Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection
  18. Heart failure and sudden cardiac death in heritable thoracic aortic disease caused by pathogenic variants in the SMAD3 gene
  19. Organisation of care for pregnancy in patients with congenital heart disease
  20. Sex, pregnancy and aortic disease in Marfan syndrome
  21. The spectrum of spontaneous coronary artery dissection: illustrated review of the literature
  22. Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trial
  23. The 2017 international classification of the Ehlers-Danlos syndromes
  24. Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome
  25. Pregnancy in Women With SMAD3 Mutation
  26. Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome
  27. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations
  28. FBN1 : The disease-causing gene for Marfan syndrome and other genetic disorders
  29. Long-Term Outcome of Patients with Perimembranous Ventricular Septal Defect: Results from the Belgian Registry on Adult Congenital Heart Disease
  30. Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse
  31. Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
  32. 2015 ESC Guidelines for the management of infective endocarditis
  33. Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans
  34. ClinGen — The Clinical Genome Resource
  35. Marfan and Sartans: time to wake up!: Figure 1
  36. Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome
  37. Arterial hypertension in Turner syndrome
  38. Managing aortic aneurysms and dissections during pregnancy
  39. Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaboration
  40. Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
  41. Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients
  42. Marfan Syndrome☆
  43. The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome
  44. Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome
  45. A different view on predictors of pulmonary hypertension in secundum atrial septal defect
  46. Reference Values for Echocardiographic Assessment of the Diameter of the Aortic Root and Ascending Aorta Spanning All Age Categories
  47. Loeys–Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signaling
  48. Treatment of pre-existing cardiomyopathy during pregnancy
  49. Absence of Cardiovascular Manifestations in a Haploinsufficient Tgfbr1 Mouse Model
  50. Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome
  51. Heart failure in pregnant women with cardiac disease: data from the ROPAC
  52. Functional analysis of the anatomical right ventricular components: should assessment of right ventricular function after repair of tetralogy of Fallot be refined?
  53. Characterization of Cardiovascular Involvement in Pseudoxanthoma Elasticum Families
  54. Worsening in oxygen saturation and exercise capacity predict adverse outcome in patients with Eisenmenger syndrome
  55. Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy
  56. Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice
  57. Echocardiographic Methods, Quality Review, and Measurement Accuracy in a Randomized Multicenter Clinical Trial of Marfan Syndrome
  58. Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy
  59. Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD
  60. Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2
  61. Predictive model for late atrial arrhythmia after closure of an atrial septal defect
  62. Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysms
  63. Multiple Aneurysms in a Patient With Aneurysms-Osteoarthritis Syndrome
  64. Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity
  65. In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg Syndrome
  66. Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria
  67. Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants
  68. The Ghent Marfan Trial — A randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockers
  69. Right Ventricular Function in Patients With Eisenmenger Syndrome
  70. Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome
  71. The importance of pulmonary artery pressures on late atrial arrhythmia in transcatheter and surgically closed ASD type secundum
  72. Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes
  73. A Quantitative Comparison Between Baseline Hemodynamics and End-Stage Aneurysm Formation in ApoE −/− Mice
  74. An Integrated Framework to Quantitatively Link Mouse-Specific Hemodynamics to Aneurysm Formation in Angiotensin II-infused ApoE −/− mice
  75. Iron deficiency is associated with adverse outcome in Eisenmenger patients
  76. PREDICTING THE OCCURRENCE OF ATRIAL ARRHYTHMIA AFTER CLOSURE OF AN ATRIAL SEPTAL DEFECT
  77. Resolving in-vivo flow fields in the systemic circulation of the mouse through combined ultrasound imaging and computational fluid dynamics
  78. Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial
  79. Cardiovascular manifestations in men and women carrying a FBN1 mutation
  80. Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndrome
  81. The revised Ghent nosology for the Marfan syndrome
  82. Expanding the phenotype of sudden cardiac death—An unusual presentation of a family with a Lamin A/C mutation
  83. The Belgian Eisenmenger syndrome registry: Implications for treatment strategies?
  84. Circulating Transforming Growth Factor-β in Marfan Syndrome
  85. Patient-Specific Modelling of Aortic Arch Wall Shear Stress Patterns in Patients With Marfan Syndrome
  86. Short-term systolic and diastolic ventricular performance after surgical ventricular restoration for dilated ischemic cardiomyopathy
  87. Marfan and Marfan-like syndromes
  88. Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic FBN1 Mutations
  89. Strain Rate Imaging Detects Early Cardiac Effects of Pegylated Liposomal Doxorubicin as Adjuvant Therapy in Elderly Patients with Breast Cancer
  90. Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature
  91. The expanding cardiovascular phenotype of Marfan syndrome
  92. Effect of an Abdominal Aortic Aneurysm on Wave Reflection in the Aorta
  93. Successful alcohol septal ablation for late recurrence of left ventricular outflow tract obstruction after surgical myectomy in hypertrophic obstructive cardiomyopathy
  94. The Impact of an Abdominal Aortic Aneurysm on Aortic Wave Reflection
  95. Marfan Syndrome
  96. Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood
  97. Synergistic inhibition of the enzymatic activity of aminopeptidase N by divalent metal ion chelators
  98. Primary impairment of left ventricular function in Marfan syndrome
  99. Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor
  100. A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndrome
  101. Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndrome
  102. Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
  103. Echocardiographically estimated left ventricular end-diastolic and right ventricular systolic pressure in normotensive healthy individuals
  104. Effects of age, gender, and left ventricular mass on septal mitral annulus velocity (E′) and the ratio of transmitral early peak velocity to E′ (E/E′)
  105. Evaluation of left ventricular dimensions and function in Marfan's syndrome without significant valvular regurgitation
  106. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
  107. Functional analysis of the common carotid artery
  108. DUP25 remains unconfirmed
  109. Diastolic dysfunction, infarct size, and exercise capacity in remote myocardial infarction: a combined approach of mitral E-wave deceleration time and color M-mode flow propagation velocity
  110. Connective Tissue Disorders