Hypertrophic Obstructive Cardiomyopathy, Bleeding History, and Acquired von Willebrand Syndrome: Response to Septal Myectomy

Por Blackshear, Joseph L., Schaff, Hartzell V., Ommen, Steve R., Chen, Dong, Nichols, William L.
Publicado em 2011

Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients with Hypertrophic Cardiomyopathy

Por Bos, J. Martijn, Will, Melissa L., Gersh, Bernard J., Kruisselbrink, Teresa M., Ommen, Steve R., Ackerman, Michael J.
Publicado no Mayo Clin Proc (2014)

Atrial Fibrillation in Hypertrophic Cardiomyopathy: Prevalence, Clinical Correlations, and Mortality in a Large High‐Risk Population

Por Siontis, Konstantinos C., Geske, Jeffrey B., Ong, Kevin, Nishimura, Rick A., Ommen, Steve R., Gersh, Bernard J.
Publicado no J Am Heart Assoc (2014)

Relation Between Temperature Extremes And Symptom Exacerbation In Patients With Hypertrophic Cardiomyopathy

Por Bois, John P., Adams, Jonathon C., Kumar, Gautam, Ommen, Steve R., Nishimura, Rick A., Klarich, Kyle W.
Publicado no Am J Cardiol (2015)

Diastolic Relaxation and Compliance Reserve during Dynamic Exercise in Heart Failure with Preserved Ejection Fraction

Por Borlaug, Barry A, Jaber, Wissam A, Ommen, Steve R, Lam, Carolyn SP, Redfield, Margaret M, Nishimura, Rick A
Publicado em 2011

Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy

Por Bos, J. Martijn, Theis, Jeanne L., Tajik, A. Jamil, Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.
Publicado em 2008

Size, Shape and Stamina: The Impact of Left Ventricular Geometry on Exercise Capacity

Por Lam, Carolyn S.P., Grewal, Jasmine, Borlaug, Barry A., Ommen, Steve R., Kane, Garvan C., McCully, Robert B., Pellikka, Patricia A.
Publicado em 2010

Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations

Por McLeod, Christopher J., Bos, J. Martijn, Theis, Jeanne L., Edwards, William D., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.
Publicado em 2009

Cardiac structure and ventricular-vascular function in persons with heart failure and preserved ejection fraction from Olmsted County, Minnesota

Por Lam, Carolyn S. P., Roger, Véronique L., Rodeheffer, Richard J., Bursi, Francesca, Borlaug, Barry A., Ommen, Steve R., Kass, David A., Redfield, Margaret M.
Publicado em 2007

Prevalence and clinical correlates of QT prolongation in patients with hypertrophic cardiomyopathy

Por Johnson, Jonathan N., Grifoni, Camilla, Bos, J. Martijn, Saber-Ayad, Maha, Ommen, Steve R., Nistri, Stefano, Cecchi, Franco, Olivotto, Iacopo, Ackerman, Michael J.
Publicado em 2011

Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy

Por Murphy, Sinead L., Anderson, Jason H., Kapplinger, Jamie D., Kruisselbrink, Teresa M., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J., Bos, J. Martijn
Publicado no J Cardiovasc Transl Res (2016)

Molecular and Functional Characterization of Novel Hypertrophic Cardiomyopathy Susceptibility Mutations in TNNC1- Encoded Troponin C

Por Landstrom, Andrew P., Parvatiyar, Michelle S., Pinto, Jose R., Marquardt, Michelle L., Bos, J. Martijn, Tester, David J., Ommen, Steve R., Potter, James D., Ackerman, Michael J.
Publicado em 2008

Genotype—phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin

Por Bos, J. Martijn, Poley, Rainer N., Ny, Melissa, Tester, David J., Xu, Xiaolei, Vatta, Matteo, Towbin, Jeffrey A., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.
Publicado em 2005

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

Por Theis, Jeanne L., Bos, J. Martijn, Theis, Jason D., Miller, Dylan V., Dearani, Joseph A., Schaff, Hartzell V., Gersh, Bernard J., Ommen, Steve R., Moss, Richard L., Ackerman, Michael J.
Publicado em 2009

Mutations in JPH2-Encoded Junctophilin-2 Associated with Hypertrophic Cardiomyopathy in Humans

Por Landstrom, Andrew P., Weisleder, Noah, Batalden, Karin B., Bos, J. Martijn, Tester, David J., Ommen, Steve R., Wehrens, Xander H.T, Claycomb, William C., Ko, Jae-Kyun, Hwang, Moonsun, Pan, Zui, Ma, Jianjie, Ackerman, Michael J.
Publicado no J Mol Cell Cardiol (2007)

Formin Homology 2 Domain Containing 3 (FHOD3) Variants Associated with Hypertrophic Cardiomyopathy

Por Wooten, Eric C., Hebl, Virginia Bartleson, Wolf, Matthew J., Greytak, Sarah R., Orr, Nicole, Draper, Isabelle, Calvino, Jenna E., Kapur, Navin K., Maron, Martin S., Kullo, Iftikhar J., Ommen, Steve R., Bos, J. Martijn, Ackerman, Michael J., Huggins, Gordon S.
Publicado em 2012

Decreased Exercise Capacity and Sleep-Disordered Breathing in Patients With Hypertrophic Cardiomyopathy

Por Konecny, Tomas, Geske, Jeffrey B., Ludka, Ondrej, Orban, Marek, Brady, Peter A., Abudiab, Muaz M., Albuquerque, Felipe N., Placek, Alexander, Kara, Tomas, Sahakyan, Karine R., Gersh, Bernard J., Tajik, A. Jamil, Allison, Thomas G., Ommen, Steve R., Somers, Virend K.
Publicado no Chest (2015)

Utility of T-wave amplitude as a non-invasive risk marker of sudden cardiac death in hypertrophic cardiomyopathy

Por Sugrue, Alan, Killu, Ammar M, DeSimone, Christopher V, Chahal, Anwar A, Vogt, Josh C, Kremen, Vaclav, Hai, JoJo, Hodge, David O, Acker, Nancy G, Geske, Jeffrey B, Ackerman, Michael J, Ommen, Steve R, Lin, Grace, Noseworthy, Peter A, Brady, Peter A
Publicado no Open Heart (2017)

Research Priorities in Hypertrophic Cardiomyopathy: Report of a Working Group of the National Heart Lung and Blood Institute

Por Force, Thomas, Bonow, Robert O., Houser, Steven R., Solaro, R. John, Hershberger, Ray E., Adhikari, Bishow, Anderson, Mark E., Boineau, Robin, Byrne, Barry J., Cappola, Thomas P., Kalluri, Raghu, LeWinter, Martin M., Maron, Martin S., Molkentin, Jeffery D., Ommen, Steve R., Regnier, Michael, Wilson Tang, W. H., Tian, Rong, Konstam, Marvin A., Maron, Barry J., Seidman, Christine E.
Publicado em 2010

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Por Purevjav, Enkhsaikhan, Arimura, Takuro, Augustin, Sibylle, Huby, Anne-Cecile, Takagi, Ken, Nunoda, Shinichi, Kearney, Debra L., Taylor, Michael D., Terasaki, Fumio, Bos, Johan M., Ommen, Steve R., Shibata, Hiroki, Takahashi, Megumi, Itoh-Satoh, Manatsu, McKenna, William J., Murphy, Ross T., Labeit, Siegfried, Yamanaka, Yoichi, Machida, Noboru, Park, Jeong-Euy, Alexander, Peta M.A., Weintraub, Robert G., Kitaura, Yasushi, Ackerman, Michael J., Kimura, Akinori, Towbin, Jeffrey A.
Publicado em 2012