Hypertrophic cardiomyopathy: a systematic review.

By B. Maron. 2002

2,341 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine

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In Cardiology and Cardiovascular Medicine

1. B. Maron
2. Steve R. Ommen
3. M. Maron
4. P. Spirito
5. C. Semsarian
6. Iacopo Olivotto
7. J. Udelson
8. Mark S. Link

Citations in the corpus

• Prevalence, Clinical Profile, and Significance of Left Ventricular Remodeling in the End-Stage Phase of Hypertrophic Cardiomyopathy (2006, methodology): “Remodeling Patterns Four patterns of LV remodeling were identified: (1) Twentythree patients (52%) showed the most complete remodeling, with LV cavity enlargement ( 55 mm end-diastolic) and/or increase in size, associated with relatively mild hypertrophy ( 20 mm), and/or regression in septal thickne”
• Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hypertrophic cardiomyopathy. (2007, methodology): “ICDs restored sinus rhythm, even in the presence of extreme functional and morphologic disease features such as marked left ventricular outflow tract obstruction and massive left ventricular hypertrophy.(2,4) Furthermore, ICDs were effective in preventing sudden arrhythmic death in virtually every p”
• Abnormal Calcium Handling Properties Underlie Familial Hypertrophic Cardiomyopathy Pathology in Patient-Specific Induced Pluripotent Stem Cells (2013, background): “…Mutation Exhibit Electrophysiological and Contractile Arrhythmia at the Single-Cell Level Arrhythmia is a clinical hallmark of HCM and is responsible for a significant portion of morbidity and mortality associated with the disease including sudden cardiac death (Maron, 2002; Maron et al., 1996).”
• Long-term effects of surgical septal myectomy on survival in patients with obstructive hypertrophic cardiomyopathy. (2005, background): “, 5% f all HCM patients) (2,5,6), and the particularly longerm follow-up that would be required.”