Aortic Dimensions, Biophysical Properties, and Plasma Biomarkers in Children and Adults with Marfan or Loeys-Dietz Syndrome
Author:
Funder
Canadian Institutes of Health Research
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference55 articles.
1. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene;Dietz;Nature,1991
2. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2;Loeys;Nat Genet,2005
3. Aneurysm syndromes caused by mutations in the TGF-beta receptor;Loeys;N Engl J Med,2006
4. Therapy of Marfan syndrome;Judge;Annu Rev Med,2008
5. Angiotensin II-dependent TGF-beta signaling contributes to Loeys-Dietz syndrome vascular pathogenesis;Gallo;J Clin Invest,2014
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1. TGFβ level in healthy and children with Marfan syndrome—effective reduction under sartan therapy;Frontiers in Pediatrics;2024-02-05
2. Are aortic biomechanical properties early markers of dilatation in patients with Marfan Syndrome? – A Systematic Review and Meta-Analysis;2024-01-07
3. Impact of Genotype-Phenotype Interactions on Cardiovascular Function in Paediatric Loeys-Dietz Syndrome;CJC Pediatric and Congenital Heart Disease;2023-12
4. A phenotypic screen of Marfan syndrome iPSC-derived vascular smooth muscle cells uncovers GSK3β as a new target;Stem Cell Reports;2023-02
5. Markers of extracellular matrix remodeling and systemic inflammation in patients with heritable thoracic aortic diseases;Frontiers in Cardiovascular Medicine;2022-12-20
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