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Autor:
Stijntje Hibender, Barbara J.M. Mulder, Carlie J.M. de Vries, Anique ter Braake, Aeilko H. Zwinderman, Maurice J. van den Hoff, Esther Lutgens, M. Groenink, Edith E. Schermer, Romy Franken, Y. M. Pinto, Cindy van Roomen, Vivian de Waard, Quinn Gunst, Ingeborg van der Made
Publikováno v:
Arteriosclerosis, thrombosis, and vascular biology, 36(8), 1618-1626. Lippincott Williams and Wilkins
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 1618-26
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 8, pp. 1618-26
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 1618-26
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 8, pp. 1618-26
Objective— Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the fibrillin-1 gene. Patients with MFS are at risk of aortic aneurysm formation and dissection. Usually, blood pressure–lowering drugs are used to reduce aor