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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 8, 2005
Genetic basis of thoracic aortic aneurysms and aortic dissectionsHariyadarshi Pannu, Van Tran-Fadulu, Dianna M MilewiczAnnals of the New York Academy of Sciences|December 22, 2006
Genetic basis of thoracic aortic aneurysms and dissections: potential relevance to abdominal aortic aneurysmsHariyadarshi Pannu, Nili Avidan, Van Tran-Fadulu, et al.Nature Clinical Practice. Cardiovascular Medicine|March 3, 2007
Severe aortic and arterial aneurysms associated with a TGFBR2 mutationScott A LeMaire, Hariyadarshi Pannu, Van Tran-Fadulu, et al.Journal of Human Genetics|September 17, 2008
An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to diseaseDong-Chuan Guo, Prateek Gupta, Van Tran-Fadulu, et al.Annual Review of Genomics and Human Genetics|June 12, 2008
Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunctionDianna M Milewicz, Dong-Chuan Guo, Van Tran-Fadulu, et al.Circulation. Cardiovascular Genetics|December 18, 2010
Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissectionDong-Chuan Guo, Ellen S Regalado, Charles Minn, et al.American Journal of Medical Genetics. Part A|August 5, 2011
Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysmsEllen Regalado, Sarah Medrek, Van Tran-Fadulu, et al.American Journal of Medical Genetics. Part A|April 29, 2006
Familial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in womenVan Tran-Fadulu, Julia H Chen, Danielle Lemuth, et al.Circulation|July 20, 2005
Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissectionsHariyadarshi Pannu, Van Tran Fadulu, Jessica Chang, et al.European Journal of Medical Genetics|November 28, 2009
Paucity of skeletal manifestations in Hispanic families with FBN1 mutationsCarlos Villamizar, Ellen S Regalado, Van Tran Fadulu, et al.Pageof 2