Hypertrophic cardiomyopathy
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Hypertrophic cardiomyopathy: interrelation of clinical manifestations, pathoophysiology, and therapy
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Hypertrophic cardiomyopathy: the importance of the site and extent of hypertrophy — a review
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Hypertrophic cardiomyopathy: a discussion of nomenclature
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Familial hypertorphic cardiomyopathy is a genetically heterogeneous disease
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Cited by (84)
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2007, Journal of Heart and Lung TransplantationCitation Excerpt :Heart failure in HCM is largely the consequence of diastolic dysfunction.27 However, approximately 10% to 15% of patients with HCM progress to left ventricular dilation and dysfunction28; in this case, there is poor systolic as well as diastolic function, and it can be speculated that the resultant decrease in perfusion pressure may predispose to renal injury. Recipients with significant hemodynamic instability pre-transplant were at increased risk for long-term renal insufficiency.
Rare clinical presentation of nonobstructive hypertrophic cardiomyopathy: Apical aneurysm with thrombus
2007, International Journal of CardiologyCitation Excerpt :Hypertrophic cardiomyopathy (HCM) is characterized by massive and often asymmetrical left ventricular (LV) and/or right ventricular hypertrophy [1,2].
Midventricular hypertrophic cardiomyopathy coexistent with anomalous origin of circumflex artery
2006, International Journal of CardiologyResting ST-segment depression predicts exercise-induced subendocardial ischemia in patients with hypertrophic cardiomyopathy
2006, International Journal of CardiologyAutoimmunity against the second extracellular loop of beta <inf>1</inf>-adrenergic receptors induces early afterdepolarization and decreases in K-channel density in rabbits
2004, Journal of the American College of Cardiology
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