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Journal of Nursing Scholarship : an Official Publication of Sigma Theta Tau International Honor Society of Nursing
|
January 7, 2006
Genomics and cardiovascular disease
Lorraine Frazier, Rolanda L Johnson, Elizabeth Sparks
Progress in Cardiovascular Nursing
|
September 10, 2009
Cardiovascular nursing on human genomics: what do cardiovascular nurses need to know about congestive heart failure?
Lorraine Frazier, Shu-Fen Wung, Elizabeth Sparks, et al.
The Journal of Cardiovascular Nursing
|
April 3, 2008
Biobanks and biomarker research in cardiovascular disease
Lorraine Frazier, Elizabeth Sparks, Jennifer E Sanner, et al.
American Journal of Medical Genetics. Part A
|
November 29, 2015
Massive hemoptysis in Loeys-Dietz syndrome
Christopher L Bennett, Hamza Aziz, Elizabeth Sparks, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 2, 2004
Abnormal left ventricular mass and aortic distensibility in pediatric dialysis patients
Renee F Robinson, Milap C Nahata, Elizabeth Sparks, et al.
Circulation. Cardiovascular Genetics
|
September 6, 2012
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy
Neal K Lakdawala, Jens J Thune, Steven D Colan, 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 women
Van 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 dissections
Hariyadarshi Pannu, Van Tran Fadulu, Jessica Chang, et al.
Journal of the American College of Cardiology
|
February 2, 2010
Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy
Neal K Lakdawala, Lisa Dellefave, Charles S Redwood, et al.
Circulation Research
|
April 10, 2010
Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy
Adam J Saltzman, Debora Mancini-DiNardo, Chumei Li, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Journal of Nursing Scholarship : an Official Publication of Sigma Theta Tau International Honor Society of Nursing
|
January 7, 2006
Genomics and cardiovascular disease
Lorraine Frazier, Rolanda L Johnson, Elizabeth Sparks
Progress in Cardiovascular Nursing
|
September 10, 2009
Cardiovascular nursing on human genomics: what do cardiovascular nurses need to know about congestive heart failure?
Lorraine Frazier, Shu-Fen Wung, Elizabeth Sparks, et al.
The Journal of Cardiovascular Nursing
|
April 3, 2008
Biobanks and biomarker research in cardiovascular disease
Lorraine Frazier, Elizabeth Sparks, Jennifer E Sanner, et al.
American Journal of Medical Genetics. Part A
|
November 29, 2015
Massive hemoptysis in Loeys-Dietz syndrome
Christopher L Bennett, Hamza Aziz, Elizabeth Sparks, et al.
Pediatric Nephrology (Berlin, Germany)
|
November 2, 2004
Abnormal left ventricular mass and aortic distensibility in pediatric dialysis patients
Renee F Robinson, Milap C Nahata, Elizabeth Sparks, et al.
Circulation. Cardiovascular Genetics
|
September 6, 2012
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy
Neal K Lakdawala, Jens J Thune, Steven D Colan, 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 women
Van 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 dissections
Hariyadarshi Pannu, Van Tran Fadulu, Jessica Chang, et al.
Journal of the American College of Cardiology
|
February 2, 2010
Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy
Neal K Lakdawala, Lisa Dellefave, Charles S Redwood, et al.
Circulation Research
|
April 10, 2010
Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy
Adam J Saltzman, Debora Mancini-DiNardo, Chumei Li, et al.
Page
of 2