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Periodontal conditions in patients with Marfan syndrome - a multicenter case control studyPerspectives on the revised Ghent criteria for the diagnosis of Marfan syndromeThe role of the multidisciplinary health care team in the management of patients with Marfan syndromeChest radiography for the diagnosis of acute aortic syndromeEconomic and care considerations of Marfan syndrome.A standardized education protocol significantly reduces traumatic injuries and syncope recurrence: an observational study in 316 patients with vasovagal syncope.Prospective risk stratification of sudden cardiac death in Marfan's syndrome.Pulse wave analysis of the aortic pressure waveform in patients with vasovagal syncope.Heart rate turbulence and deceleration capacity for risk prediction of serious arrhythmic events in Marfan syndrome.Inpatient rehabilitation for adult patients with Marfan syndrome: an observational pilot study.Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse.A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm.The economic impact of Marfan syndrome: a non-experimental, retrospective, population-based matched cohort study.Induction of macrophage chemotaxis by aortic extracts from patients with Marfan syndrome is related to elastin binding protein.Overexpression of Gremlin-1 in patients with Loeys-Dietz syndrome: implications on pathophysiology and early disease detection.Marfan syndrome: an update of genetics, medical and surgical management.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.Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations.Analysis of Strengths, Weaknesses, Opportunities, and Threats as a Tool for Translating Evidence into Individualized Medical Strategies (I-SWOT).Ambulatory (24 h) blood pressure and arterial stiffness measurement in Marfan syndrome patients: a case control feasibility and pilot study.Vascular type Ehlers-Danlos syndrome is associated with platelet dysfunction and low vitamin D serum concentration.The importance of genetic testing in the clinical management of patients with Marfan syndrome and related disorders.Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.The Value of Circulating Biomarkers in Bicuspid Aortic Valve-Associated Aortopathy.Late post-AVR progression of bicuspid aortopathy: link to hemodynamics.Aortopathy in Bicuspid Aortic Valve Stenosis with Fusion of Right-Left versus Right-Non-Coronary Cusps: Are These Different Diseases?Morphologic and Functional Markers of Aortopathy in Patients With Bicuspid Aortic Valve Insufficiency Versus Stenosis.Branched versus fenestrated endografts for endovascular repair of aortic arch lesions.Diagnostic accuracy study of routine echocardiography for bicuspid aortic valve: a retrospective study and meta-analysis.Indomethacin Prevents the Progression of Thoracic Aortic Aneurysm in Marfan Syndrome Mice.Diagnosis and management of Marfan syndrome.Interpretation of sequence variants of the FBN1 gene: analog or digital? A commentary on decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants.Complete Antegrade Transapical Deployment of a Branched Aortic Arch Endograft: A Porcine Feasibility Study.Severe eczema and Hyper-IgE in Loeys-Dietz-syndrome - contribution to new findings of immune dysregulation in connective tissue disorders.Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in ChildhoodAddendum.Retrospective analysis of the effect of angiotensin II receptor blocker versus β-blocker on aortic root growth in paediatric patients with Marfan syndrome.FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression.Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice.
P50
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P50
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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Yskert von Kodolitsch
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