Clinical genetics

Citations 1-7 of 7 total displayed.

Most recent content (1 Nov 2009):

Original Articles
Dysfunctional Corin I555(P568) Allele Is Associated With Impaired Brain Natriuretic Peptide Processing and Adverse Outcomes in Blacks With Systolic Heart Failure: Results From the Genetic Risk Assessment in Heart Failure Substudy

J. Eduardo Rame, S. William Tam, Dennis McNamara, Manuel Worcel, Michael L. Sabolinski, Alan H. Wu, and Daniel L. Dries
Circ Heart Fail 2009;2:541-548; published online before print as doi:10.1161/CIRCHEARTFAILURE.109.866822 [Abstract] [Full text]  

Images and Case Reports in Heart Failure
Impaired Systolic Function in Loeys-Dietz Syndrome: A Novel Cardiomyopathy?

Peter M. Eckman, Eileen Hsich, E. Rene Rodriguez, Gonzalo V. Gonzalez-Stawinski, Rocio Moran, and David O. Taylor
Circ Heart Fail 2009;2:707-708, doi:10.1161/CIRCHEARTFAILURE.109.888636 [Full text]  

Past content (since May 2009):

Original Article
An _2C-Adrenergic Receptor Polymorphism Alters the Norepinephrine Lowering Effects and Therapeutic Response of the Beta Blocker Bucindolol in Chronic Heart Failure

Michael R. Bristow, Guinevere A. Murphy, Heidi Krause-Steinrauf, Jeffrey L. Anderson, John F. Carlquist, Surai Thaneemit-Chen, Vaishali Krishnan, William T. Abraham, Brian D. Lowes, J. David Port, Gordon W. Davis, Laura C. Lazzeroni, Alastair D. Robertson, Philip W. Lavori, and Stephen B. Liggett
Circ Heart Fail published October 30, 2009, doi:10.1161/CIRCHEARTFAILURE.109.885962 [Abstract]  

Original Article
Dysfunctional Corin I555 (P568) Allele is Associated with Impaired BNP Processing and Adverse Outcomes in African-Americans with Systolic Heart Failure: Results from the Genetic Risk Assessment in Heart Failure A-HeFT Sub-Study

J. Eduardo Rame, William Tam, Dennis McNamara, Manuel Worcel, Michael L. Sabolinski, Alan Wu, and Daniel L. Dries
Circ Heart Fail published September 28, 2009, doi:10.1161/CIRCHEARTFAILURE.109.866822 [Abstract]  

Images and Case Reports in Heart Failure
Heart Failure and Cardiac Involvement as Isolated Manifestation of Familial Form of Transthyretin Amyloidosis Resulting From Val30Met Mutation With No Clinical Signs of Polyneuropathy

Daniel C. Christoph, Dirk Boese, Kristian T.M. Johnson, Thomas W. Schlosser, Peter Hunold, Hideo A. Baba, Raimund Erbel, and Sebastian Philipp
Circ Heart Fail 2009;2:512-515, doi:10.1161/CIRCHEARTFAILURE.109.853697 [Full text]  

Original Article
Expression Patterns of Cardiac Myofilament Proteins - Genomic and Protein Analysis of Surgical Myectomy Tissue from Patients with Obstructive Hypertrophic Cardiomyopathy

Jeanne L. Theis, Johan Martijn Bos, Jason D. Theis, Dylan V. Miller, Joseph A. Dearani, Hartzell V. Schaff, Bernard J. Gersh, Steve R. Ommen, Richard L. Moss, and Michael J. Ackerman
Circ Heart Fail published May 13, 2009, doi:10.1161/CIRCHEARTFAILURE.108.789735 [Abstract]  

Advances in Heart Failure
Progress With Genetic Cardiomyopathies: Screening, Counseling, and Testing in Dilated, Hypertrophic, and Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Ray E. Hershberger, Jason Cowan, Ana Morales, and Jill D. Siegfried
Circ Heart Fail 2009;2:253-261, doi:10.1161/CIRCHEARTFAILURE.108.817346 [Abstract] [Full text]