Loeys-Dietz Syndrome
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Elsevier
Reference9 articles.
1. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2;Loeys;Nat Genet,2005
2. Aneurysm syndromes caused by mutations in the TGF-beta receptor;Loeys;New Engl J Med,2006
3. Loeys-Dietz syndrome: a primer for diagnosis and management;Maccarrick;Genet Med,2014
4. Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis;van de Laar;Nat Genet,2011
5. Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm;Lindsay;Nat Genet,2012
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1. TGFβ prevents IgE-mediated allergic disease by restraining T follicular helper 2 differentiation;Science Immunology;2024-01-19
2. Unusual presentation of Loeys-Dietz syndrome: A case report of clinical findings and treatment challenges;World Journal of Clinical Cases;2022-11-26
3. Molecular Imaging of Aortic Aneurysm and Its Translational Power for Clinical Risk Assessment;Frontiers in Medicine;2022-04-15
4. Skeletal Deformities in Osterix-Cre;Tgfbr2f/f Mice May Cause Postnatal Death;Genes;2021-06-25
5. Imaging evaluation of uterine perforation and rupture;Abdominal Radiology;2021-06-15
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