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Journal ArticleDOI

American Society of Echocardiography clinical recommendations for multimodality cardiovascular imaging of patients with hypertrophic cardiomyopathy: Endorsed by the American Society of Nuclear Cardiology, Society for Cardiovascular Magnetic Resonance, and Society of Cardiovascular Computed Tomography.

TLDR
This research presents a meta-analyses of the determinants of infectious disease outbreaks in eight operation theatres across the United States and Canada over a period of 12 months in the period of May 21 to 29, 2012.
Abstract
Sherif F. Nagueh, MD, FASE, Chair,* S. Michelle Bierig, RDCS, FASE,* Matthew J. Budoff, MD, Milind Desai, MD,* Vasken Dilsizian, MD, Benjamin Eidem, MD, FASE,* Steven A. Goldstein, MD,* Judy Hung, MD, FASE,* Martin S. Maron, MD, Steve R. Ommen, MD,* and Anna Woo, MD,*Houston, Texas; St. Louis, Missouri; Los Angeles, California; Cleveland, Ohio; Baltimore, Maryland; Rochester, Minnesota; Washington, District of Columbia; Boston, Massachusetts; Toronto, Ontario, Canada

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Journal ArticleDOI

Echocardiography in Hypertrophic Cardiomyopathy: In with Strain, Out with Straining?

TL;DR: Echocardiography has helped elucidate numerous mechanisms for these abnormalities and is the primary imaging modality used in the screening, diagnosis, and intraprocedural and long-term monitoring of patients with HCM.
Journal ArticleDOI

Differences in the extent of fibrosis in obstructive and nonobstructive hypertrophic cardiomyopathy.

TL;DR: LVOT obstruction may play a role in the extent of fibrosis in HCM, possibly conditioning greater diastolic dysfunction.
Journal ArticleDOI

Differentiating physiology from pathology in elite athletes. Left ventricular hypertrophy versus hypertrophic cardiomyopathy

TL;DR: Hubert Krysztofiak, MD, PhD is the Head of the National Centre for Sports Medicine and an investigator at the Mossakowski Medical Research Centre of Polish Academy of Sciences, responsible for the medical care for Olympians.
Journal ArticleDOI

Ventricular Arrhythmia in Septal and Apical Hypertrophic Cardiomyopathy: The French-Canadian Experience.

TL;DR: The phenotype of apical HCM is much more common in French-Canadians of Caucasian descent compared to other Caucasian HCM populations and was associated with an increased risk of ventricular arrhythmia even when excluding patients with apical aneurysm.
References
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Journal ArticleDOI

Recommendations for the evaluation of left ventricular diastolic function by echocardiography

TL;DR: The assessment of left ventricular (LV) diastolic function and filling pressures is of paramount clinical importance to distinguish this syndrome from other diseases such as pulmonary disease resulting in dyspnea, to assess prognosis, and to identify underlying cardiac disease and its best treatment.
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