All Stories

  1. The ‘Ten Commandments’ for the 2025 ESC Guidelines on Cardiovascular Disease and Pregnancy
  2. Preventing cardiovascular complications in adults with congenital heart disease: predictors and outcomes of the levels of follow-up care
  3. Translating the Latest 2025 ESC Guidelines and Consensus Statement into Acute Cardiovascular Care Practice
  4. 2025 ESC Guidelines for the management of cardiovascular disease and pregnancy
  5. The challenges of decision-making in managing women with prosthetic heart valves during pregnancy: a global concern
  6. Pregnancy outcomes in women with heritable thoracic aortic disease: data from the EORP ESC registry of pregnancy and cardiac disease (ROPAC) III
  7. Systematic disruption of zebrafish fibrillin genes identifies a translational zebrafish model for Marfan syndrome
  8. Differences in Arterial Events in Vascular Ehlers-Danlos, Loeys-Dietz, and Marfan Syndrome
  9. Editor's Choice – A European Delphi Consensus on the Management of Abdominal Aortic Aneurysms in Patients with Heritable Aortic Diseases
  10. Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve
  11. Assessment of Myocardial Fibrosis in Marfan Syndrome Using Cardiac Magnetic Resonance Imaging
  12. Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations
  13. Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve
  14. 2024 ESC Guidelines for the management of peripheral arterial and aortic diseases
  15. Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations
  16. Bicuspid Aortic Valve Disease with Early-Onset Complications: Characteristics and Aortic Outcomes
  17. Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium
  18. Bicuspid Aortic Valve Disease With Early Onset Complications: Characteristics And Aortic Outcomes
  19. Three-dimensional co-culturing of stem cell-derived cardiomyocytes and cardiac fibroblasts reveals a role for both cell types in Marfan-related cardiomyopathy
  20. Biological Age in Congenital Heart Disease—Exploring the Ticking Clock
  21. Application of an automated analysis framework for pulsed-wave Doppler cardiac ultrasound measurements to generate reference data in adult zebrafish
  22. Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve
  23. Refining the course: long-term outcome in patients with bicuspid aortic valve
  24. Long-term follow-up of atrioventricular valve function in Fontan patients: effect of atrioventricular valve surgery
  25. Shedding light on type B aortic dissection in Marfan syndrome: implications for patient counselling and research priorities
  26. Fluid-Structure Interaction Modeling of the Aortic Hemodynamics in Adult Zebrafish: A Pilot Study Based on Synchrotron X-Ray Tomography
  27. Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stage
  28. Genetic Testing in Patients With Congenital Heart Disease: You Do No Harm When Using the Right Tools!
  29. Mitral Annular Disjunction: Associated Pathologies and Clinical Consequences
  30. Last year of life of adults with congenital heart diseases: causes of death and patterns of care
  31. Hereditary thoracic aortic disease: How to save lives
  32. Needs and Experiences of Adolescents with Congenital Heart Disease and Parents in the Transitional Process: A Qualitative Study
  33. Association of Mitral Annular Disjunction With Cardiovascular Outcomes Among Patients With Marfan Syndrome
  34. Marfan syndrome
  35. Influenza Vaccination in Patients With Congenital Heart Disease in the Pre-COVID-19 Era: Coverage Rate, Patient Characteristics, and Outcomes
  36. Outflow Through Aortic Side Branches Drives False Lumen Patency in Type B Aortic Dissection
  37. An Overview of Investigational and Experimental Drug Treatment Strategies for Marfan Syndrome
  38. Transition to adulthood and transfer to adult care of adolescents with congenital heart disease: a global consensus statement of the ESC Association of Cardiovascular Nursing and Allied Professions (ACNAP), the ESC Working Group on Adult Congenital Hea...
  39. Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO
  40. QRS Duration During Follow-Up of Tetralogy of Fallot: How Valuable is it? Analysis of ECG Changes in Relation to Pulmonary Valve Implantation
  41. Guía ESC 2020 para el tratamiento de las cardiopatías congénitas del adulto
  42. Different levels of care for follow-up of adults with congenital heart disease: a cost analysis scrutinizing the impact on medical costs, hospitalizations, and emergency department visits
  43. Transfer and transition practices in 96 European adult congenital heart disease centres
  44. Pregnancy outcome in thoracic aortic disease data from the Registry Of Pregnancy And Cardiac disease
  45. Pregnancy Outcomes in Women After Arterial Switch Operation for Transposition of the Great Arteries: Results From ROPAC (Registry of Pregnancy and Cardiac Disease) of the European Society of Cardiology EURObservational Research Programme
  46. A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations
  47. Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm
  48. The Dynamic and Multifaceted Nature of Cardiovascular Disease and Using Genetic Testing to Inform Clinical Care: An International Perspective
  49. Genética en la cardiopatía congénita: ¿estamos preparados?
  50. The ESC Clinical Practice Guidelines for the Management of Adult Congenital Heart Disease 2020
  51. The ‘Ten Commandments’ in Adult Congenital Heart Disease Guidelines
  52. Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study
  53. Effects of fibrillin mutations on the behavior of heart muscle cells in Marfan syndrome
  54. Creating the BELgian COngenital heart disease database combining administrative and clinical data (BELCODAC): Rationale, design and methodology
  55. Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review
  56. Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome
  57. 2020 ESC Guidelines for the management of adult congenital heart disease
  58. MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking Water
  59. Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice
  60. A new dimension in patent foramen ovale size estimation
  61. Pregnancy Outcomes in Women With Cardiovascular Disease: Evolving Trends Over 10 Years in the ESC Registry of Pregnancy and Cardiac Disease (ROPAC)
  62. Corrosion casting of the cardiovascular structure in adult zebrafish for analysis by scanning electron microscopy and X‐ray microtomography
  63. Long-Term Healthcare Utilization, Medical Cost, and Societal Cost in Adult Congenital Heart Disease
  64. Features of Marfan syndrome not listed in the Ghent nosology – The Dark Side of the Disease
  65. Angiotensin-II receptor blockade in Marfan syndrome
  66. Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome
  67. Development of a transition program for adolescents with congenital heart disease
  68. European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants
  69. Genetic testing for aortopathies
  70. Opinions of general and adult congenital heart disease cardiologists on care for adults with congenital heart disease in Belgium: a qualitative study
  71. Correction: Arterial tortuosity syndrome: 40 new families and literature review
  72. Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome
  73. 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...
  74. Real-world healthcare utilization in adult congenital heart disease: a systematic review of trends and ratios
  75. Disproportion and dysmorphism in an adult Belgian population with Turner syndrome: risk factors for chronic diseases?
  76. Staffing, activities, and infrastructure in 96 specialised adult congenital heart disease clinics in Europe
  77. Vascular Ehlers-Danlos Syndrome Management
  78. SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections
  79. Reply
  80. Body mass index in adults with congenital heart disease
  81. SMAD3 pathogenic variants: risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium
  82. OUP accepted manuscript
  83. Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome
  84. Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association
  85. Arterial tortuosity syndrome: 40 new families and literature review
  86. Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
  87. Cardiovascular imaging in Turner syndrome: state-of-the-art practice across the lifespan
  88. Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection
  89. Hepatic Changes in the Fontan Circulation: Identification of Liver Dysfunction and an Attempt to Streamline Follow-up Screening
  90. A heart for fibrillin: spatial arrangement in adult wild-type murine myocardial tissue
  91. Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome
  92. Looking for the Missing Links
  93. Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome
  94. Heart failure and sudden cardiac death in heritable thoracic aortic disease caused by pathogenic variants in the SMAD3 gene
  95. Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome
  96. Hungarian Marfan family with large FBN1 deletion calls attention to copy number variation detection in the current NGS era
  97. Pregnancy Outcomes in Women With Rheumatic Mitral Valve Disease
  98. Propagation-based phase-contrast synchrotron imaging of aortic dissection in mice: from individual elastic lamella to 3D analysis
  99. Influence of socioeconomic factors on pregnancy outcome in women with structural heart disease
  100. Organisation of care for pregnancy in patients with congenital heart disease
  101. Sex, pregnancy and aortic disease in Marfan syndrome
  102. Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting
  103. The spectrum of spontaneous coronary artery dissection: illustrated review of the literature
  104. 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
  105. Pregnancy in women with hypertrophic cardiomyopathy: data from the European Society of Cardiology initiated Registry of Pregnancy and Cardiac disease (ROPAC)
  106. The 2017 international classification of the Ehlers-Danlos syndromes
  107. Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome
  108. Pregnancy in Women With SMAD3 Mutation
  109. Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome
  110. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations
  111. FBN1 : The disease-causing gene for Marfan syndrome and other genetic disorders
  112. Risk of Pregnancy in Moderate and Severe Aortic Stenosis
  113. Ventricular tachyarrhythmia during pregnancy in women with heart disease: Data from the ROPAC, a registry from the European Society of Cardiology
  114. Long-Term Outcome of Patients with Perimembranous Ventricular Septal Defect: Results from the Belgian Registry on Adult Congenital Heart Disease
  115. Pulmonary hypertension and pregnancy outcomes: data from the Registry Of Pregnancy and Cardiac Disease (ROPAC) of the European Society of Cardiology
  116. Global cardiac risk assessment in the Registry Of Pregnancy And Cardiac disease: results of a registry from the European Society of Cardiology
  117. Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse
  118. Guía ESC 2015 sobre el tratamiento de la endocarditis infecciosa
  119. Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches
  120. Type B aortic dissection triggered by heart transplantation in a patient with Marfan syndrome
  121. Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia
  122. Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
  123. 2015 ESC Guidelines for the management of infective endocarditis
  124. Pregnancy in Women With a Mechanical Heart Valve
  125. Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans
  126. ClinGen — The Clinical Genome Resource
  127. Marfan and Sartans: time to wake up!: Figure 1
  128. Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome
  129. Arterial hypertension in Turner syndrome
  130. Managing aortic aneurysms and dissections during pregnancy
  131. 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
  132. Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
  133. Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients
  134. Marfan Syndrome☆
  135. MAT2A Mutations Predispose Individuals to Thoracic Aortic Aneurysms
  136. 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
  137. Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome
  138. A different view on predictors of pulmonary hypertension in secundum atrial septal defect
  139. Reference Values for Echocardiographic Assessment of the Diameter of the Aortic Root and Ascending Aorta Spanning All Age Categories
  140. Loeys–Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signaling
  141. Treatment of pre-existing cardiomyopathy during pregnancy
  142. Absence of Cardiovascular Manifestations in a Haploinsufficient Tgfbr1 Mouse Model
  143. Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome
  144. New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections
  145. Heart failure in pregnant women with cardiac disease: data from the ROPAC
  146. First report of the genetic background of Marfan syndrome in Polish patients
  147. Functional analysis of the anatomical right ventricular components: should assessment of right ventricular function after repair of tetralogy of Fallot be refined?
  148. Characterization of Cardiovascular Involvement in Pseudoxanthoma Elasticum Families
  149. Worsening in oxygen saturation and exercise capacity predict adverse outcome in patients with Eisenmenger syndrome
  150. Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy
  151. Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice
  152. Echocardiographic Methods, Quality Review, and Measurement Accuracy in a Randomized Multicenter Clinical Trial of Marfan Syndrome
  153. Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy
  154. Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD
  155. Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2
  156. Predictive model for late atrial arrhythmia after closure of an atrial septal defect
  157. Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysms
  158. Multiple Aneurysms in a Patient With Aneurysms-Osteoarthritis Syndrome
  159. Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity
  160. In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg Syndrome
  161. Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria
  162. Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants
  163. The Ghent Marfan Trial — A randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockers
  164. Right Ventricular Function in Patients With Eisenmenger Syndrome
  165. Questioning the Pathogenic Role of the GLA p.Ala143Thr “Mutation” in Fabry Disease: Implications for Screening Studies and ERT
  166. Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome
  167. The importance of pulmonary artery pressures on late atrial arrhythmia in transcatheter and surgically closed ASD type secundum
  168. Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes
  169. A Quantitative Comparison Between Baseline Hemodynamics and End-Stage Aneurysm Formation in ApoE −/− Mice
  170. The new Ghent criteria for Marfan syndrome: what do they change?
  171. An Integrated Framework to Quantitatively Link Mouse-Specific Hemodynamics to Aneurysm Formation in Angiotensin II-infused ApoE −/− mice
  172. Iron deficiency is associated with adverse outcome in Eisenmenger patients
  173. PREDICTING THE OCCURRENCE OF ATRIAL ARRHYTHMIA AFTER CLOSURE OF AN ATRIAL SEPTAL DEFECT
  174. Resolving in-vivo flow fields in the systemic circulation of the mouse through combined ultrasound imaging and computational fluid dynamics
  175. Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial
  176. Dilated cardiomyopathy caused by a novel TNNT2 mutation—Added value of genetic testing in the correct identification of affected subjects
  177. Cardiovascular manifestations in men and women carrying a FBN1 mutation
  178. Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndrome
  179. The revised Ghent nosology for the Marfan syndrome
  180. Expanding the phenotype of sudden cardiac death—An unusual presentation of a family with a Lamin A/C mutation
  181. The Belgian Eisenmenger syndrome registry: Implications for treatment strategies?
  182. Circulating Transforming Growth Factor-β in Marfan Syndrome
  183. Patient-Specific Modelling of Aortic Arch Wall Shear Stress Patterns in Patients With Marfan Syndrome
  184. Short-term systolic and diastolic ventricular performance after surgical ventricular restoration for dilated ischemic cardiomyopathy
  185. Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion
  186. Marfan and Marfan-like syndromes
  187. 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
  188. Strain Rate Imaging Detects Early Cardiac Effects of Pegylated Liposomal Doxorubicin as Adjuvant Therapy in Elderly Patients with Breast Cancer
  189. Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature
  190. Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation
  191. The expanding cardiovascular phenotype of Marfan syndrome
  192. A pilot study to investigate the feasibility and cardiac effects of pegylated liposomal doxorubicin (PL-DOX) as adjuvant therapy in medically fit elderly breast cancer patients
  193. Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions
  194. Effect of an Abdominal Aortic Aneurysm on Wave Reflection in the Aorta
  195. Successful alcohol septal ablation for late recurrence of left ventricular outflow tract obstruction after surgical myectomy in hypertrophic obstructive cardiomyopathy
  196. Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
  197. Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families
  198. Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study
  199. Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome
  200. The Impact of an Abdominal Aortic Aneurysm on Aortic Wave Reflection
  201. Early Surgical Experience With Loeys-Dietz: A New Syndrome of Aggressive Thoracic Aortic Aneurysm Disease
  202. Marfan Syndrome
  203. 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
  204. Experimental and numerical assessment of the impact of abdominal aortic aneurysms on arterial wave reflection
  205. Synergistic inhibition of the enzymatic activity of aminopeptidase N by divalent metal ion chelators
  206. Primary impairment of left ventricular function in Marfan syndrome
  207. Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor
  208. A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndrome
  209. Aortic reflection coefficients and their association with global indexes of wave reflection in healthy controls and patients with Marfan's syndrome
  210. Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndrome
  211. Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
  212. Echocardiographically estimated left ventricular end-diastolic and right ventricular systolic pressure in normotensive healthy individuals
  213. The use of Tissue Doppler Imaging for the assessment of changes in myocardial structure and function in inherited cardiomyopathies
  214. 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′)
  215. Evaluation of left ventricular dimensions and function in Marfan's syndrome without significant valvular regurgitation
  216. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
  217. Comprehensive molecular screening of theFBN1gene favors locus homogeneity of classical Marfan syndrome
  218. Functional analysis of the common carotid artery
  219. DUP25 remains unconfirmed
  220. Familiale aandoeningen van de thoracale aorta
  221. 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
  222. Parameters of inflammation and infection in a community based case-control study of coronary heart disease
  223. QT dispersion is not related to infarct size or inducibility in patients with coronary artery disease and life threatening ventricular arrhythmias
  224. Connective Tissue Disorders