Marfan syndrome-Reference-Cited by-同舟云学术

Marfan syndrome

Published:2012-08 Issue:4 Volume:24 Page:498-504
ISSN:1040-8703
Container-title:Current Opinion in Pediatrics
language:en
Short-container-title:

Author:

Bolar Nikhita,Van Laer Lut,Loeys Bart L.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pediatrics, Perinatology and Child Health

Reference31 articles.

1. A case of congenital malformation of the four limbs, most pronounced in the extremities, characterized by an extension of the bones with a certain degree of slimming (in French).;Marfan;Bulletins et memoires de la Societe medicale des Hopitaux de Paris,1886

2. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.;Dietz;Nature,1991

3. Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.;Habashi;Science,2006

4. Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome.;Judge;J Clin Invest,2004

5. Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome.;Neptune;Nat Genet,2003

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