Zoekresultaten - Carolyn Y. Ho

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  1. 1
    Genetics and Clinical Destiny: Improving Care in Hypertrophic Cardiomyopathy

    Genetics and Clinical Destiny: Improving Care in Hypertrophic Cardiomyopathy door Carolyn Y. Ho

    Gepubliceerd in 2010
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  2. 2
    Hypertrophic Cardiomyopathy in 2012

    Hypertrophic Cardiomyopathy in 2012 door Carolyn Y. Ho

    Gepubliceerd in 2012
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  3. 3
    A Clinician’s Guide to Tissue Doppler Imaging

    A Clinician’s Guide to Tissue Doppler Imaging door Carolyn Y. Ho, Scott D. Solomon

    Gepubliceerd in 2006
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  4. 4
    A Contemporary Approach to Hypertrophic Cardiomyopathy

    A Contemporary Approach to Hypertrophic Cardiomyopathy door Carolyn Y. Ho, Christine E. Seidman

    Gepubliceerd in 2006
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  5. 5
    Genetic Testing in Hypertrophic Cardiomyopathy

    Genetic Testing in Hypertrophic Cardiomyopathy door Catherine G. Ireland, Carolyn Y. Ho

    Gepubliceerd in 2024
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  6. 6
    Genetics of hypertrophic cardiomyopathy: established and emerging implications for clinical practice

    Genetics of hypertrophic cardiomyopathy: established and emerging implications for clinical practice door Luís R. Lopes, Carolyn Y Ho, Perry Elliott

    Gepubliceerd in 2024
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  7. 7
    Meta-Analysis of Penetrance and Systematic Review on Transition to Disease in Genetic Hypertrophic Cardiomyopathy

    Meta-Analysis of Penetrance and Systematic Review on Transition to Disease in Genetic Hypertrophic Cardiomyopathy door Constantin‐Cristian Topriceanu, Alexandre C. Pereira, James Moon, Gabriella Captur, Carolyn Y. Ho

    Gepubliceerd in 2023
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  8. 8
    Ω-Net (Omega-Net): Fully automatic, multi-view cardiac MR detection, orientation, and segmentation with deep neural networks

    Ω-Net (Omega-Net): Fully automatic, multi-view cardiac MR detection, orientation, and segmentation with deep neural networks door Davis M. Vigneault, Weidi Xie, Carolyn Y. Ho, David A. Bluemke, J. Alison Noble

    Gepubliceerd in 2018
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  9. 9
    Research priorities in sarcomeric cardiomyopathies

    Research priorities in sarcomeric cardiomyopathies door Jolanda van der Velden, Carolyn Y. Ho, Jil C. Tardiff, Iacopo Olivotto, Björn C. Knollmann, L. Carrier

    Gepubliceerd in 2015
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  10. 10
    Genetic advances in sarcomeric cardiomyopathies: state of the art

    Genetic advances in sarcomeric cardiomyopathies: state of the art door Carolyn Y. Ho, Philippe Charron, Pascale Richard, Francesca Girolami, Karin Y. van Spaendonck‐Zwarts, Yigal M. Pinto

    Gepubliceerd in 2015
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  11. 11
    Homozygous Mutation in Cardiac Troponin T

    Homozygous Mutation in Cardiac Troponin T door Carolyn Y. Ho, Harry M. Lever, Roman W. DeSanctis, Carol Farver, Jonathan G. Seidman, Christine E. Seidman

    Gepubliceerd in 2000
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  12. 12
    Intracerebral Hemorrhage and Ischemic Stroke of Different Etiologies Have Distinct Alternatively Spliced mRNA Profiles in the Blood: a Pilot RNA-seq Study

    Intracerebral Hemorrhage and Ischemic Stroke of Different Etiologies Have Distinct Alternatively Spliced mRNA Profiles in the Blood: a Pilot RNA-seq Study door Cheryl Dykstra-Aiello, Glen C. Jickling, Bradley P. Ander, Xinhua Zhan, Dazhi Liu, Heather Hull, Miles Orantia, Carolyn Y. Ho, Boryana Stamova

    Gepubliceerd in 2015
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  13. 13
    The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

    The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance door Radwa Noureldin, Songtao Liu, Marcelo Souto Nacif, Daniel P. Judge, Marc K. Halushka, Theodore P. Abraham, Carolyn Y. Ho, David A. Bluemke

    Gepubliceerd in 2012
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  14. 14
    Cardiovascular manifestations of Fabry disease: relationships between left ventricular hypertrophy, disease severity, and -galactosidase A activity

    Cardiovascular manifestations of Fabry disease: relationships between left ventricular hypertrophy, disease severity, and -galactosidase A activity door Justina Wu, Carolyn Y. Ho, Hicham Skali, Rekha Abichandani, W. R. Wilcox, Maryam Banikazemi, Seymour Packman, Katherine B. Sims, Scott D. Solomon

    Gepubliceerd in 2010
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  15. 15
    Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

    Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations door Francesca Girolami, Carolyn Y. Ho, Christopher Semsarian, Massimo Baldi, Melissa L. Will, Katia Baldini, Francesca Torricelli, Laura Yeates, Franco Cecchi, Michael J. Ackerman, Iacopo Olivotto

    Gepubliceerd in 2010
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  16. 16
    Sex‐Related Differences in Genetic Cardiomyopathies

    Sex‐Related Differences in Genetic Cardiomyopathies door Alessia Argirò, Carolyn Y. Ho, Sharlene M. Day, Jolanda van der Velden, Elisabetta Cerbai, Sara Saberi, Jil C. Tardiff, Neal K. Lakdawala, Iacopo Olivotto

    Gepubliceerd in 2022
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  17. 17
    Intrinsic mitral valve alterations in hypertrophic cardiomyopathy sarcomere mutation carriers

    Intrinsic mitral valve alterations in hypertrophic cardiomyopathy sarcomere mutation carriers door John D. Groarke, Patrycja Galazka, Allison L. Cirino, Neal K. Lakdawala, Jens Jakob Thune, Henning Bundgaard, E. John Orav, Robert A. Levine, Carolyn Y. Ho

    Gepubliceerd in 2018
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  18. 18
    Study Design and Rationale of EXPLORER-HCM

    Study Design and Rationale of EXPLORER-HCM door Carolyn Y. Ho, Iacopo Olivotto, Daniel Jacoby, Steven J. Lester, Matthew T. Roe, Andrew Wang, Cynthia Burstein Waldman, David Zhang, Amy J. Sehnert, Stephen B. Heitner

    Gepubliceerd in 2020
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  19. 19
    Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): health status analysis of a randomised, double-blind, placebo-controlled, phase 3 trial

    Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): health status analysis of a randomised, double-blind, placebo-controlled, phase 3 tr... door John A. Spertus, Jennifer Fine, Perry Elliott, Carolyn Y. Ho, Iacopo Olivotto, Sara Saberi, Wanying Li, Chantal Dolan, Matthew Reaney, Amy J. Sehnert, Daniel Jacoby

    Gepubliceerd in 2021
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  20. 20
    Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2

    Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2 door Carolyn Y. Ho, Brith Otterud, RD Legare, Tena Varvil, Ruchi Saxena, DB DeHart, SE Kohler, JC Aster, S. Bruce Dowton, FP Li, Mark Leppert, DG Gilliland

    Gepubliceerd in 1996
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