Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2849444 | American Heart Journal | 2013 | 11 Pages |
Abstract
Baseline demographic, clinical, and anthropometric characteristics of the randomized cohort are representative of patients in this population with moderate to severe aortic root dilation. The high percentage of young subjects with relatives who have had aortic dissection or surgery illustrates the need for more definitive therapy; we expect that the results of the study and the wealth of systematic data collected will make an important contribution to the management of individuals with Marfan syndrome.
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Authors
Ronald V. MD, Lin T. PhD, Harry C. MD, Gail D. MD, ScD, Anji T. MD, Bruce D. MD, Bart L. MD, PhD, D. Woodrow MD, PhD, Timothy J. MBChB, Julie MD, PhD, Geoffrey A. MD, Gloria L. MS, RD, Wyman W. MD, MPH, Jami C. MS, MD, Mark B. MD, Larry W. MD,