Aortic root complications in Marfan's syndrome: identification of a lower risk group.

Author:

Legget M. E.,Unger T. A.,O'Sullivan C. K.,Zwink T. R.,Bennett R. L.,Byers P. H.,Otto C. M.

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference20 articles.

1. The Marfan syndrome;Pyeritz, R.E.,1992

2. Life expectancy and causes of death in the Marfan syndrome;Murdoch, J.L.; Walker, B.A.; Halpem, B.L.; Kuzma, J.W.; McKussick, V.A.;NEnglJtMed,1972

3. Marfan's syndrome: natural history and long-term follow-up of cardiovascular involvement;Marsalese, D.L.; Moodie, D.S.; Vacante, M.; Lytle, B.W.; Gill, C.C.; Sterta, R.;J7 Am Coil Cardiol,1989

4. Prognostic significance of the pattern of aortic root dilation in the Marfan syndrome;Roman, M.J.; Rosen, S.E.; Kramer-Fox, R.; Devereux, R.B.;J Am Coll Cardiol,1993

5. The natural history of aortic dilation in Marfan syndrome;Hwa, J.; Richards, J.G.; Huang, M.; McKay, D.; Pressley, L.; Hughes, C.F.;MedJAust,1993

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