Losartan Added to β-Blockade Therapy for Aortic Root Dilation in Marfan Syndrome: A Randomized, Open-Label Pilot Study
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference19 articles.
1. β-Blocker therapy does not alter the rate of aortic root dilation in pediatric patients with Marfan syndrome;Selamet Tierney;J Pediatr,2007
2. The effect of β-blocker therapy on clinical outcome in patients with Marfan's syndrome: a meta-analysis;Gersony;Int J Cardiol,2007
3. Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome;Habashi;Science,2006
4. Latent transforming growth factor β-binding protein 1 interacts with fibrillin and is a microfibril-associated protein;Isogai;J Biol Chem,2003
5. Angiotensin II blockade reverse myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy;Lim;Circulation,2001
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1. Management of aortic disease in children with FBN1-related Marfan syndrome;European Heart Journal;2024-09-09
2. Multidisciplinary follow-up in a patient with Morgagni hernia leads to diagnosis of Marfan syndrome;Italian Journal of Pediatrics;2024-05-07
3. Ameliorative Effect of Coenzyme Q10 on Phenotypic Transformation in Human Smooth Muscle Cells with FBN1 Knockdown;International Journal of Molecular Sciences;2024-02-25
4. TGFβ level in healthy and children with Marfan syndrome—effective reduction under sartan therapy;Frontiers in Pediatrics;2024-02-05
5. Hereditary Thoracic Aortic Diseases;Diagnostics;2024-01-04
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