Differential contribution of elastin and fibrillin-1 to the cardiovascular phenotype of a double heterozygous Marfan and Williams-Beuren syndrome mouse model
Source
Genes and Diseases - ISSN 2352-4820-14:2 (2027) p.
Introducing allopurinol to the medical treatment of Marfan syndrome : advantages, limitations, and potential extension to other aortopathies
Source
Cardiovascular drugs and therapy - ISSN 0920-3206- (2026) p.
Sex-and age-dependent neurovascular abnormalities linked to neuroinflammation lead to exacerbated post-ischemic brain injury in Marfan syndrome mice
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Redox Biology - ISSN 2213-2317-83 (2025) p. 1-23
Extracellular vesicles as mediators of endothelial dysfunction in cardiovascular diseases
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International journal of molecular sciences - ISSN 1661-6596-26:3 (2025) p. 1-19
Navigating toward gene therapy in Marfan syndrome : a hope for halting aortic aneurysm
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Molecular Therapy. Methods & Clinical Development - ISSN 2329-0501-32:1 (2024) p. 1-2