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- Journal Article
- A1
- open access
Angiotensin receptor blockers and β blockers in Marfan syndrome : an individual patient data meta-analysis of randomised trials
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Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
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- Journal Article
- A1
- open access
Physical activity intensity, bout-duration, and cardiometabolic risk markers in children and adolescents
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Clinical utility gene card for: hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches
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- Journal Article
- A1
- open access
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
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The new Ghent criteria for Marfan syndrome: what do they change ?
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In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome
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Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year
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Cardiovascular manifestations in men and women carrying a FBN1 mutation
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Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]