All Stories

  1. Prevention of Heart Failure in Women: An Expert Consensus Statement on Sex-Specific Risk Factors
  2. Evaluation of the Diagnostic Yield of Exome-Based Panels for Congenital Heart Defects in Different Clinical Settings
  3. Accelerated epigenetic ageing in congenital heart disease: the AccelerAGE study
  4. Decoding Mitral Valve Risk in Marfan Syndrome
  5. Diagnosis and management of heritable thoracic aortic diseases
  6. The ‘Ten Commandments’ for the 2025 ESC Guidelines on Cardiovascular Disease and Pregnancy
  7. Preventing cardiovascular complications in adults with congenital heart disease: predictors and outcomes of the levels of follow-up care
  8. Translating the Latest 2025 ESC Guidelines and Consensus Statement into Acute Cardiovascular Care Practice
  9. Valve-Sparing Root Replacement in Bicuspid and Tricuspid Aortic Valves: Long-Term Outcomes Into the Second Decade
  10. 2025 ESC Guidelines for the management of cardiovascular disease and pregnancy
  11. The challenges of decision-making in managing women with prosthetic heart valves during pregnancy: a global concern
  12. How sample handling distorts telomere studies
  13. Pregnancy outcomes in women with heritable thoracic aortic disease: data from the EORP ESC registry of pregnancy and cardiac disease (ROPAC) III
  14. Systematic disruption of zebrafish fibrillin genes identifies a translational zebrafish model for Marfan syndrome
  15. Novel Aortic Dissection Model Links Endothelial Dysfunction and Immune Infiltration
  16. Differences in Arterial Events in Vascular Ehlers-Danlos, Loeys-Dietz, and Marfan Syndrome
  17. Editor's Choice – A European Delphi Consensus on the Management of Abdominal Aortic Aneurysms in Patients with Heritable Aortic Diseases
  18. 2024 ESC Guidelines for the management of peripheral arterial and aortic diseases (Translation of the shortened document prepared by the Czech Society of Cardiology)
  19. 2024 ESC Guidelines for the management of peripheral arterial and aortic diseases (Translation of the summary of the document prepared by the Czech Society of Angiology, 2025)
  20. Pregnancy with a prosthetic heart valve, thrombosis, and bleeding: the ESC EORP Registry of Pregnancy and Cardiac disease III
  21. Pregnancy-related issues in rare and low-prevalence diseases: results of ERN transversal working group on pregnancy and family planning survey
  22. Linee guida ESC 2024 per la gestione delle patologie delle arterie periferiche e dell’aorta
  23. Interpretation and classification of FBN1 variants associated with Marfan syndrome: consensus recommendations from the Clinical Genome Resource’s FBN1 variant curation expert panel
  24. Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve
  25. Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease: results from the Montalcino Aortic Consortium
  26. New insights into the structural role of EMILINs within the human skin microenvironment
  27. Assessment of Myocardial Fibrosis in Marfan Syndrome Using Cardiac Magnetic Resonance Imaging
  28. Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications
  29. Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations
  30. Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve
  31. Perinatal outcomes after in-utero exposure to beta-blockers in women with heart disease: Data from the ESC EORP registry of pregnancy and cardiac disease (ROPAC)
  32. 2024 ESC Guidelines for the management of peripheral arterial and aortic diseases
  33. Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations
  34. Surveillance of adults with congenital heart disease: Current guidelines and actual clinical practice
  35. Bicuspid Aortic Valve Disease with Early-Onset Complications: Characteristics and Aortic Outcomes
  36. Anterior scleral thickness in Marfan syndrome: A quantitative analysis
  37. Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium
  38. A novel genetic mouse model of fatal aortic dissection reveals massive inflammatory cell infiltration in the thoracic aorta
  39. Bicuspid Aortic Valve Disease With Early Onset Complications: Characteristics And Aortic Outcomes
  40. Frailty and Cognitive Function in Middle-Aged and Older Adults With Congenital Heart Disease
  41. Three-dimensional co-culturing of stem cell-derived cardiomyocytes and cardiac fibroblasts reveals a role for both cell types in Marfan-related cardiomyopathy
  42. Evaluation of a nurse-led multi-component transition program for adolescents with congenital heart disease
  43. Biological Age in Congenital Heart Disease—Exploring the Ticking Clock
  44. Application of an automated analysis framework for pulsed-wave Doppler cardiac ultrasound measurements to generate reference data in adult zebrafish
  45. An Appealing Story of Sex Differences in Marfan Syndrome
  46. Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse models
  47. Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve
  48. Refining the course: long-term outcome in patients with bicuspid aortic valve
  49. Long-term follow-up of atrioventricular valve function in Fontan patients: effect of atrioventricular valve surgery
  50. Shedding light on type B aortic dissection in Marfan syndrome: implications for patient counselling and research priorities
  51. Fluid-Structure Interaction Modeling of the Aortic Hemodynamics in Adult Zebrafish: A Pilot Study Based on Synchrotron X-Ray Tomography
  52. Preferences for disease-related information and transitional skills among adolescents with congenital heart disease in the early transitional stage
  53. Genetic Testing in Patients With Congenital Heart Disease: You Do No Harm When Using the Right Tools!
  54. Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing
  55. HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN
  56. Mitral Annular Disjunction: Associated Pathologies and Clinical Consequences
  57. Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials
  58. Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)
  59. Last year of life of adults with congenital heart diseases: causes of death and patterns of care
  60. Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease
  61. Cardiolaminopathies
  62. Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study
  63. Publisher Correction: Marfan syndrome
  64. Hereditary thoracic aortic disease: How to save lives
  65. Needs and Experiences of Adolescents with Congenital Heart Disease and Parents in the Transitional Process: A Qualitative Study
  66. Association of Mitral Annular Disjunction With Cardiovascular Outcomes Among Patients With Marfan Syndrome
  67. Marfan syndrome
  68. Influenza Vaccination in Patients With Congenital Heart Disease in the Pre-COVID-19 Era: Coverage Rate, Patient Characteristics, and Outcomes
  69. Outflow Through Aortic Side Branches Drives False Lumen Patency in Type B Aortic Dissection
  70. An Overview of Investigational and Experimental Drug Treatment Strategies for Marfan Syndrome
  71. Cardiomyopathy in Genetic Aortic Diseases
  72. 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...
  73. Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO
  74. QRS Duration During Follow-Up of Tetralogy of Fallot: How Valuable is it? Analysis of ECG Changes in Relation to Pulmonary Valve Implantation
  75. Guía ESC 2020 para el tratamiento de las cardiopatías congénitas del adulto
  76. Congenital heart disease in the ESC EORP Registry of Pregnancy and Cardiac disease (ROPAC)
  77. 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
  78. Transfer and transition practices in 96 European adult congenital heart disease centres
  79. Pregnancy outcome in thoracic aortic disease data from the Registry Of Pregnancy And Cardiac disease
  80. 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
  81. A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations
  82. Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm
  83. The Dynamic and Multifaceted Nature of Cardiovascular Disease and Using Genetic Testing to Inform Clinical Care: An International Perspective
  84. Genética en la cardiopatía congénita: ¿estamos preparados?
  85. The ESC Clinical Practice Guidelines for the Management of Adult Congenital Heart Disease 2020
  86. The ‘Ten Commandments’ in Adult Congenital Heart Disease Guidelines
  87. Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study
  88. Effects of fibrillin mutations on the behavior of heart muscle cells in Marfan syndrome
  89. Creating the BELgian COngenital heart disease database combining administrative and clinical data (BELCODAC): Rationale, design and methodology
  90. Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review
  91. Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome
  92. 2020 ESC Guidelines for the management of adult congenital heart disease
  93. MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking Water
  94. Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice
  95. A new dimension in patent foramen ovale size estimation
  96. Pregnancy Outcomes in Women With Cardiovascular Disease: Evolving Trends Over 10 Years in the ESC Registry of Pregnancy and Cardiac Disease (ROPAC)
  97. Corrosion casting of the cardiovascular structure in adult zebrafish for analysis by scanning electron microscopy and X‐ray microtomography
  98. Long-Term Healthcare Utilization, Medical Cost, and Societal Cost in Adult Congenital Heart Disease
  99. Features of Marfan syndrome not listed in the Ghent nosology – The Dark Side of the Disease
  100. Angiotensin-II receptor blockade in Marfan syndrome
  101. Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome
  102. Development of a transition program for adolescents with congenital heart disease
  103. European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants
  104. Genetic testing for aortopathies
  105. Opinions of general and adult congenital heart disease cardiologists on care for adults with congenital heart disease in Belgium: a qualitative study
  106. Correction: Arterial tortuosity syndrome: 40 new families and literature review
  107. Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome
  108. 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...
  109. Real-world healthcare utilization in adult congenital heart disease: a systematic review of trends and ratios
  110. Disproportion and dysmorphism in an adult Belgian population with Turner syndrome: risk factors for chronic diseases?
  111. Staffing, activities, and infrastructure in 96 specialised adult congenital heart disease clinics in Europe
  112. Vascular Ehlers-Danlos Syndrome Management
  113. SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections
  114. Reply
  115. Body mass index in adults with congenital heart disease
  116. SMAD3 pathogenic variants: risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium
  117. OUP accepted manuscript
  118. Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome
  119. Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association
  120. Arterial tortuosity syndrome: 40 new families and literature review
  121. Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
  122. Cardiovascular imaging in Turner syndrome: state-of-the-art practice across the lifespan
  123. Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection
  124. Hepatic Changes in the Fontan Circulation: Identification of Liver Dysfunction and an Attempt to Streamline Follow-up Screening
  125. A heart for fibrillin: spatial arrangement in adult wild-type murine myocardial tissue
  126. Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome
  127. Looking for the Missing Links
  128. 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
  129. Heart failure and sudden cardiac death in heritable thoracic aortic disease caused by pathogenic variants in the SMAD3 gene
  130. Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome
  131. Hungarian Marfan family with large FBN1 deletion calls attention to copy number variation detection in the current NGS era
  132. Pregnancy Outcomes in Women With Rheumatic Mitral Valve Disease
  133. Propagation-based phase-contrast synchrotron imaging of aortic dissection in mice: from individual elastic lamella to 3D analysis
  134. Influence of socioeconomic factors on pregnancy outcome in women with structural heart disease
  135. Organisation of care for pregnancy in patients with congenital heart disease
  136. Sex, pregnancy and aortic disease in Marfan syndrome
  137. Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting
  138. The spectrum of spontaneous coronary artery dissection: illustrated review of the literature
  139. 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
  140. Pregnancy in women with hypertrophic cardiomyopathy: data from the European Society of Cardiology initiated Registry of Pregnancy and Cardiac disease (ROPAC)
  141. The 2017 international classification of the Ehlers-Danlos syndromes
  142. Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome
  143. Pregnancy in Women With SMAD3 Mutation
  144. Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome
  145. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations
  146. FBN1 : The disease-causing gene for Marfan syndrome and other genetic disorders
  147. Risk of Pregnancy in Moderate and Severe Aortic Stenosis
  148. Ventricular tachyarrhythmia during pregnancy in women with heart disease: Data from the ROPAC, a registry from the European Society of Cardiology
  149. Long-Term Outcome of Patients with Perimembranous Ventricular Septal Defect: Results from the Belgian Registry on Adult Congenital Heart Disease
  150. Pulmonary hypertension and pregnancy outcomes: data from the Registry Of Pregnancy and Cardiac Disease (ROPAC) of the European Society of Cardiology
  151. Linee guida ESC 2015 per il trattamento dell’endocardite infettiva. Task Force per il Trattamento dell’Endocardite Infettiva della Società Europea di Cardiologia (ESC)
  152. Global cardiac risk assessment in the Registry Of Pregnancy And Cardiac disease: results of a registry from the European Society of Cardiology
  153. Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse
  154. Guía ESC 2015 sobre el tratamiento de la endocarditis infecciosa
  155. Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches
  156. Type B aortic dissection triggered by heart transplantation in a patient with Marfan syndrome
  157. Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia
  158. Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
  159. 2015 ESC Guidelines for the management of infective endocarditis
  160. Pregnancy in Women With a Mechanical Heart Valve
  161. Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans
  162. ClinGen — The Clinical Genome Resource
  163. Marfan and Sartans: time to wake up!: Figure 1
  164. Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome
  165. Arterial hypertension in Turner syndrome
  166. Managing aortic aneurysms and dissections during pregnancy
  167. 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
  168. Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
  169. Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients
  170. Marfan Syndrome☆
  171. MAT2A Mutations Predispose Individuals to Thoracic Aortic Aneurysms
  172. 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
  173. Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome
  174. A different view on predictors of pulmonary hypertension in secundum atrial septal defect
  175. Reference Values for Echocardiographic Assessment of the Diameter of the Aortic Root and Ascending Aorta Spanning All Age Categories
  176. Loeys–Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signaling
  177. Treatment of pre-existing cardiomyopathy during pregnancy
  178. Absence of Cardiovascular Manifestations in a Haploinsufficient Tgfbr1 Mouse Model
  179. Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome
  180. New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections
  181. Heart failure in pregnant women with cardiac disease: data from the ROPAC
  182. First report of the genetic background of Marfan syndrome in Polish patients
  183. Functional analysis of the anatomical right ventricular components: should assessment of right ventricular function after repair of tetralogy of Fallot be refined?
  184. Characterization of Cardiovascular Involvement in Pseudoxanthoma Elasticum Families
  185. Worsening in oxygen saturation and exercise capacity predict adverse outcome in patients with Eisenmenger syndrome
  186. Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy
  187. Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice
  188. Echocardiographic Methods, Quality Review, and Measurement Accuracy in a Randomized Multicenter Clinical Trial of Marfan Syndrome
  189. Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy
  190. Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD
  191. Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2
  192. Predictive model for late atrial arrhythmia after closure of an atrial septal defect
  193. Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysms
  194. Multiple Aneurysms in a Patient With Aneurysms-Osteoarthritis Syndrome
  195. Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity
  196. In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg Syndrome
  197. Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria
  198. Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants
  199. The Ghent Marfan Trial — A randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockers
  200. Right Ventricular Function in Patients With Eisenmenger Syndrome
  201. Questioning the Pathogenic Role of the GLA p.Ala143Thr “Mutation” in Fabry Disease: Implications for Screening Studies and ERT
  202. Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome
  203. The importance of pulmonary artery pressures on late atrial arrhythmia in transcatheter and surgically closed ASD type secundum
  204. Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes
  205. A Quantitative Comparison Between Baseline Hemodynamics and End-Stage Aneurysm Formation in ApoE −/− Mice
  206. The new Ghent criteria for Marfan syndrome: what do they change?
  207. An Integrated Framework to Quantitatively Link Mouse-Specific Hemodynamics to Aneurysm Formation in Angiotensin II-infused ApoE −/− mice
  208. Iron deficiency is associated with adverse outcome in Eisenmenger patients
  209. PREDICTING THE OCCURRENCE OF ATRIAL ARRHYTHMIA AFTER CLOSURE OF AN ATRIAL SEPTAL DEFECT
  210. Resolving in-vivo flow fields in the systemic circulation of the mouse through combined ultrasound imaging and computational fluid dynamics
  211. Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial
  212. Dilated cardiomyopathy caused by a novel TNNT2 mutation—Added value of genetic testing in the correct identification of affected subjects
  213. Cardiovascular manifestations in men and women carrying a FBN1 mutation
  214. Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndrome
  215. The revised Ghent nosology for the Marfan syndrome
  216. Expanding the phenotype of sudden cardiac death—An unusual presentation of a family with a Lamin A/C mutation
  217. The Belgian Eisenmenger syndrome registry: Implications for treatment strategies?
  218. Circulating Transforming Growth Factor-β in Marfan Syndrome
  219. Patient-Specific Modelling of Aortic Arch Wall Shear Stress Patterns in Patients With Marfan Syndrome
  220. Short-term systolic and diastolic ventricular performance after surgical ventricular restoration for dilated ischemic cardiomyopathy
  221. 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
  222. Marfan and Marfan-like syndromes
  223. 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
  224. Strain Rate Imaging Detects Early Cardiac Effects of Pegylated Liposomal Doxorubicin as Adjuvant Therapy in Elderly Patients with Breast Cancer
  225. Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature
  226. Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation
  227. The expanding cardiovascular phenotype of Marfan syndrome
  228. 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
  229. Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions
  230. Effect of an Abdominal Aortic Aneurysm on Wave Reflection in the Aorta
  231. Successful alcohol septal ablation for late recurrence of left ventricular outflow tract obstruction after surgical myectomy in hypertrophic obstructive cardiomyopathy
  232. Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
  233. Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families
  234. 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
  235. Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome
  236. The Impact of an Abdominal Aortic Aneurysm on Aortic Wave Reflection
  237. Early Surgical Experience With Loeys-Dietz: A New Syndrome of Aggressive Thoracic Aortic Aneurysm Disease
  238. Marfan Syndrome
  239. 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
  240. Experimental and numerical assessment of the impact of abdominal aortic aneurysms on arterial wave reflection
  241. Synergistic inhibition of the enzymatic activity of aminopeptidase N by divalent metal ion chelators
  242. Primary impairment of left ventricular function in Marfan syndrome
  243. Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor
  244. A critical analysis of minor cardiovascular criteria in the diagnostic evaluation of patients with Marfan syndrome
  245. Aortic reflection coefficients and their association with global indexes of wave reflection in healthy controls and patients with Marfan's syndrome
  246. Variability of aortic stiffness is not associated with the fibrillin 1 genotype in patients with Marfan's syndrome
  247. Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
  248. Echocardiographically estimated left ventricular end-diastolic and right ventricular systolic pressure in normotensive healthy individuals
  249. The use of Tissue Doppler Imaging for the assessment of changes in myocardial structure and function in inherited cardiomyopathies
  250. 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′)
  251. Evaluation of left ventricular dimensions and function in Marfan's syndrome without significant valvular regurgitation
  252. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
  253. Comprehensive molecular screening of theFBN1gene favors locus homogeneity of classical Marfan syndrome
  254. Functional analysis of the common carotid artery
  255. DUP25 remains unconfirmed
  256. Familiale aandoeningen van de thoracale aorta
  257. 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
  258. Parameters of inflammation and infection in a community based case-control study of coronary heart disease
  259. QT dispersion is not related to infarct size or inducibility in patients with coronary artery disease and life threatening ventricular arrhythmias
  260. Connective Tissue Disorders